15979-82-5

• 

• Basic information

  1. Product Name: 3-methyl-N-(4-nitrophenyl)aniline
  2. Synonyms: 3-METHYL-N-(4-NITROPHENYL)BENZENAMINE
  3. CAS NO:15979-82-5
  4. Molecular Formula: C₁₃H₁₂N₂O₂
  5. Molecular Weight: 228.2466
  6. EINECS: N/A
  7. Product Categories: N/A
  8. Mol File: 15979-82-5.mol
  9. Article Data: 6

• Chemical Properties

  1. Melting Point: N/A
  2. Boiling Point: 388.6°C at 760 mmHg
  3. Flash Point: 188.8°C
  4. Appearance: N/A
  5. Density: 1.243g/cm³
  6. Vapor Pressure: 3.02E-06mmHg at 25°C
  7. Refractive Index: 1.65
  8. Storage Temp.: N/A
  9. Solubility: N/A
  10. CAS DataBase Reference: 3-methyl-N-(4-nitrophenyl)aniline(CAS DataBase Reference)
  11. NIST Chemistry Reference: 3-methyl-N-(4-nitrophenyl)aniline(15979-82-5)
  12. EPA Substance Registry System: 3-methyl-N-(4-nitrophenyl)aniline(15979-82-5)

• Safety Data

  1. Hazard Codes: N/A
  2. Statements: N/A
  3. Safety Statements: N/A
  4. WGK Germany:
  5. RTECS:
  6. HazardClass: N/A
  7. PackingGroup: N/A
  8. Hazardous Substances Data: 15979-82-5(Hazardous Substances Data)

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• SDS
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• Downstream Products
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15979-82-5 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 15979-82-5 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 1,5,9,7 and 9 respectively; the second part has 2 digits, 8 and 2 respectively.
Calculate Digit Verification of CAS Registry Number 15979-82:
(7*1)+(6*5)+(5*9)+(4*7)+(3*9)+(2*8)+(1*2)=155
155 % 10 = 5
So 15979-82-5 is a valid CAS Registry Number.

15979-82-5SDS

SAFETY DATA SHEETS

According to Globally Harmonized System of Classification and Labelling of Chemicals (GHS) - Sixth revised edition

Version: 1.0

Creation Date: Aug 16, 2017

Revision Date: Aug 16, 2017

1.Identification

1.1 GHS Product identifier

Product name	3-Methyl-N-(4-nitrophenyl)aniline

1.2 Other means of identification

Product number	-
Other names	4-nitro-3'-methyl-diphenyl amine

1.3 Recommended use of the chemical and restrictions on use

Identified uses	For industry use only.
Uses advised against	no data available

1.4 Supplier's details

1.5 Emergency phone number

Emergency phone number	-
Service hours	Monday to Friday, 9am-5pm (Standard time zone: UTC/GMT +8 hours).

More Details:15979-82-5 SDS

15979-82-5Upstream product

• 1798-11-4 4-nitrophenoxyacetic acid 
• 350-46-9 4-Fluoronitrobenzene 
• 108-44-1 1-amino-3-methylbenzene 
• 108-39-4 3-methyl-phenol 
• 100-01-6 4-nitro-aniline 
• 100-32-3 di(p-nitrophenyl) disulfide 
• 26760-22-5 methyl p-nitrobenzenesulphinate 
• 625-95-6 3-Iodotoluene 
• 621-29-4 3-tolyl isocyanate 
• 20142-88-5 2-(4-nitrophenoxy)acetyl chloride 
• 392237-47-7 2-(4-nitro-phenoxy)-N-m-tolyl-acetamide 

15979-82-5Downstream Products

• 225381-71-5 N-(6-phenyl-thieno[3,2-d]pyrimidin-4-yl)-N'-m-tolyl-benzene-1,4-diamine 
• 42771-90-4 N¹-(m-tolyl)benzene-1,4-diamine 

15979-82-5Relevant articles and documents

Diarylamine Synthesis via Desulfinylative Smiles Rearrangement

Sephton, Thomas,Large, Jonathan M.,Butterworth, Sam,Greaney, Michael F.

, p. 1132 - 1135 (2022/02/09)

Diarylamines are obtained directly from sulfinamides through a novel rearrangement sequence. The transformation is transition metal-free and proceeds under mild conditions, providing facile access to highly sterically hindered diarylamines that are otherw

Smiles rearrangement for the synthesis of diarylamines

Tian, Xiao,Wu, Ren-Min,Liu, Gang,Li, Zhu-Bo,Wei, He-Lin,Yang, Hao,Shin, Dong-Soo,Wang, Li-Ying,Zuo, Hua

experimental part, p. 118 - 126 (2011/10/02)

A protocol for the one-pot synthesis of diarylamines via Smiles rearrangement under microwave irradiation has been developed. Various diarylamines were effectively synthesized starting from readily available substituted phenols, arylamines and chloroacetyl chloride in moderate to good yields (58-92%). ARKAT-USA, Inc.

Thienopyrimidine and thienopyridine derivatives useful as anticancer agents

-

, (2008/06/13)

The invention relates to compounds of the formulas 1 and 2 and to pharmaceutically acceptable salts and hydrates thereof, wherein X1, R1, R2and R11are as defined herein. The invention also relates to pharmaceutical compositions containing the compounds of formulas 1 and 2 and to methods of treating hyperproliferative disorders in a mammal by administering the compounds of formulas 1 and 2.

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