2-methyl-4-nitroaniline

CAS No 99

C7H8N2O2 2-Methyl-4-nitroaniline 99-52-5 Min Order: 1 Metric Ton FOB Price: USD $ 0 0-0 0/Metric Ton Our company was built in 2009 with an ISO certificate In the past 5 years we have grown up as a famous fine chemicals supplier in China and we had established stable business relationships with Samsung LG Merck Thermo Fisher Scientific and so

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2

2-Amino-5-nitrotoluene / (2-Methyl-4-nitroaniline) CAS-No : 99-52-5 Formula: C7H8N2O2 Mol weight: 152 15: Solvent: Methanol Concentration: Volume: Anzahl: In den Warenkorb Auf den Merkzettel AGB Datenschutz Impressum NEOCHEMA Wald Wir nutzen Cookies auf unserer Website um diese laufend fr Sie zu verbessern

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2

2-Methyl-4-nitroaniline: Catalog No : 683568: Relevant identified uses of the substance or mixture: Identified: Laboratory chemical uses: RD: Uses advised against: HPC Standards Am Wieseneck 7 04451 Cunnersdorf Deutschland Tel +49 34291 3372-36 Fax +49 34291 3372-39 contacthpc-standards : HAZARDS IDENTIFICATION: 2 1 Classification of the

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2

2-methyl-4-nitroaniline: SMILES: CC1=C(C=CC(=C1)[N+](=O)[O-])N: Specifications Melting Point: 129C to 133C: Color: Brown or Khaki to Yellow: Packaging: Glass bottle: Infrared Spectrum: Authentic: Quantity: 5g: CAS Min % 98 5: CAS Max % 100 0: Assay Percent Range: 98 5% min (GC) Linear Formula: CH 3 C 6 H 3 (NO 2)NH 2: Beilstein : 12 846: Solubility

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4

The compounds (1) was synthesized by the reaction of ferrocene with the diazonium salt of 2- methyl- 4-nitroaniline The 1H NMR spectrum of 1 showed that unsubstituted cp-ring of ferrocene displayed singlet for five protons at 4 14 ppm however the substituted cp-ring of ferrocene splited into two signals and appeared in the region of 4 25- 4 42 ppm

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Single Crystal Growth of

Single crystal of N‐benzyl‐2‐methyl‐4‐nitroaniline (BNA) a potential organic nonlinear optical (NLO) material for terahertz (THz) pulse generation is grown successfully from diffusion controlled melt environment by Czochralski pulling (Cz) technique and is reported for the first time A solution grown crystal having habitual morphology is used as a seed with

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CAS No 99

C7H8N2O2 2-Methyl-4-nitroaniline 99-52-5 Min Order: 1 Metric Ton FOB Price: USD $ 0 0-0 0/Metric Ton Our company was built in 2009 with an ISO certificate In the past 5 years we have grown up as a famous fine chemicals supplier in China and we had established stable business relationships with Samsung LG Merck Thermo Fisher Scientific and so

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Single Crystal Growth of

Single crystal of N‐benzyl‐2‐methyl‐4‐nitroaniline (BNA) a potential organic nonlinear optical (NLO) material for terahertz (THz) pulse generation is grown successfully from diffusion controlled melt environment by Czochralski pulling (Cz) technique and is reported for the first time A solution grown crystal having habitual morphology is used as a seed with

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4

The compounds (1) was synthesized by the reaction of ferrocene with the diazonium salt of 2- methyl- 4-nitroaniline The 1H NMR spectrum of 1 showed that unsubstituted cp-ring of ferrocene displayed singlet for five protons at 4 14 ppm however the substituted cp-ring of ferrocene splited into two signals and appeared in the region of 4 25- 4 42 ppm

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System of Registries

2-Methyl-4-nitroaniline Molecular Weight: 152 15 Molecular Formula: C7H8N2O2 Additional Metadata For more information about the substance you may click one of the links below to take you to the relevant section: Program and regulatory information about this substance including

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Regioselectivity of aniline and toluidine nitration with

regioselectivity is controlled by its +R effect (45% 2 -methyl-4 -nitroaniline) and by the +I effect of the methyl group (33% 2 -methyl-5 -nitroaniline) Overall it was shown that the +R effect of the acetamide groups is stronger than that of the succinimide group This is due to the presence of one more carbonyl group in the latter which

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Single Crystal Growth of

Single crystal of N‐benzyl‐2‐methyl‐4‐nitroaniline (BNA) a potential organic nonlinear optical (NLO) material for terahertz (THz) pulse generation is grown successfully from diffusion controlled melt environment by Czochralski pulling (Cz) technique and is reported for the first time A solution grown crystal having habitual morphology is used as a seed with

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OSA

We firstly obtained organic N-benzyl-2-methyl-4-nitroaniline (BNA) single crystals using solution growth method The crystal quality obtained by solution growth method was much better than that of crystals grown by the Bridgman method Furthermore using difference frequency generation (DFG) in solution-grown BNA we generated ultra-wideband tunable THz radiation

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N

Predicted data is generated using the US Environmental Protection Agency's EPISuite™ Log Octanol-Water Partition Coef (SRC): Log Kow (KOWWIN v1 67 estimate) = 3 97 Boiling Pt Melting Pt Vapor Pressure Estimations (MPBPWIN v1 42): Boiling Pt (deg C): 371 23 (Adapted Stein Brown method) Melting Pt (deg C): 139 46 (Mean or Weighted MP) VP(mm Hg 25 deg

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Solubility and preferential solvation of 2

The mole fraction solubility of 2-methyl-4-nitroaniline in binary mixed solvents of (ethyl acetate + methanol) (ethyl acetate + ethanol) (ethyl acetate + n-propanol) and (ethyl acetate + isopropanol) was determined experimentally by using static method at temperatures from (278 15 to 313 15) K under atmospheric pressure The solubility increased with increasing temperature

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US4151203A

Process for the preparation of certain substituted p-nitroaniline compounds essentially free of the corresponding o-nitroaniline compounds The process comprises subjecting an alkanol solution of the anilides of such compounds to alkaline hydrolysis conditions thereby effecting hydrolysis and precipitation of the p-nitroaniline compound essentially free of the undesired o-isomer

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Growth optical and thermal studies on N

Benzyl 2-methyl-4-nitroaniline (BNA) is an N-derivative of MNA and it easily crystallizes and affords a larger quadratic optical nonlinearity than MNA [2] Through the optical rectification process a strong THz electromagnetic wave can be generated In this paper first we describe the growth of a BNA single crystal

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N

Abstract N-Methyl-4-nitroaniline (MNA) is used as an additive to lower the melting temperature of energetic materials in the synthesis of insensitive explosives This chemical is commonly used as an intermediate in the synthesis of dyes antioxidants pharmaceuticals and gasoline in gum inhibitors poultry medicines and as a corrosion inhibitor

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2

2-Methyl-4-nitroaniline 99-52-5 route of synthesis 2-Methyl-4-nitroaniline chemical synthesis methods 2-Methyl-4-nitroaniline synthetic routes ect +86-400-6021-666 servicemolbase Sign in Register About Us Chinese Search Batch Search Example 2163-42-0 15186-48-8 13463-67-7 57-55-6 107-43-7 56-81-5 Current Page: Home › Compound

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2

2-Methyl-4-nitroaniline 99-52-5 MSDS report 2-Methyl-4-nitroaniline MSDS safety technical specifications search 2-Methyl-4-nitroaniline safety information specifications ect +86-400-6021-666 servicemolbase Sign in Register About Us Chinese Search Batch Search Example 2163-42-0 15186-48-8 13463-67-7 57-55-6 107-43-7 56-81-5 Current Page: Home ›

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OSA

We performed the direct measurement of second harmonic generation and sum frequency generation phase-matching directions in the organic N-benzyl-2-methyl-4-nitroaniline crystal over its visible and near-infrared transparency range The fit of these data allowed us to refine the Sellmeier equations of the three principal refractive indices in this range

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Growth of N

N-benzyl-2-methyl-4-nitroaniline (BNA) fiber single crystals were grown by the micro-pulling down (-PD) method Crucible material and its shape were selected based on wetting of the crucible material by liquid BNA As a result BNA fiber single crystal with about 1–2 mm diameter was successfully grown

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Sika Chemicals Technical Grade 2

2-Methyl-4-Nitroaniline (99-52-5) is yellow powder Storage: Keep container tightly closed Keep container in a cool well-ventilated area Waste Disposal: Waste must be disposed of in accordance with federal state and local environmental control regulations

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2

2-Methyl-4-nitroaniline Weight: 152 153 g/mol: Formula: C 7 H 8 N 2 O 2: Hydrogen Acceptors: 3: Hydrogen Donors: 1: Aromatic Rings: 1: Rotatable Bonds: 1: 2-Methyl-4-nitroaniline (99-52-5) Score: #232 in Materials science #1527 in Physics #4545 in Chemistry What do you need help with? LabBot Procurement Synthesis Safety Alternatives Testing Regulation Suppliers

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N

N-ETHYL-2-METHYL-4-NITROANILINE is basic Reacts exothermically with acids to form salts plus water May be incompatible with isocyanates halogenated organics peroxides phenols (acidic) epoxides anhydrides and acid halides Reaction with strong reducing agents such as hydrides may generate flammable gaseous hydrogen

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2

2-Methyl-4-nitroaniline: Catalog No : 683568: Relevant identified uses of the substance or mixture: Identified: Laboratory chemical uses: RD: Uses advised against: HPC Standards Am Wieseneck 7 04451 Cunnersdorf Deutschland Tel +49 34291 3372-36 Fax +49 34291 3372-39 contacthpc-standards: HAZARDS IDENTIFICATION

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Growth optical and thermal studies on N

Benzyl 2-methyl-4-nitroaniline (BNA) is an N-derivative of MNA and it easily crystallizes and affords a larger quadratic optical nonlinearity than MNA [2] Through the optical rectification process a strong THz electromagnetic wave can be generated In this paper first we describe the growth of a BNA single crystal

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