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15979-85-8

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15979-85-8 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 15979-85-8 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 5 respectively.
Calculate Digit Verification of CAS Registry Number 15979-85:
(7*1)+(6*5)+(5*9)+(4*7)+(3*9)+(2*8)+(1*5)=158
158 % 10 = 8
So 15979-85-8 is a valid CAS Registry Number.

15979-85-8SDS

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-chloro-N-(4-nitrophenyl)aniline

1.2 Other means of identification

Product number -
Other names 3-CHLORO-N-(4-NITROPHENYL)BENZENAMINE

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:15979-85-8 SDS

15979-85-8Downstream Products

15979-85-8Relevant articles and documents

Ligand-Enabled Gold-Catalyzed C(sp2)-N Cross-Coupling Reactions of Aryl Iodides with Amines

Akram, Manjur O.,Das, Avishek,Chakrabarty, Indradweep,Patil, Nitin T.

supporting information, p. 8101 - 8105 (2019/10/11)

The first example of ancillary (P,N)-ligand-enabled gold-catalyzed C-N cross-coupling reactions of aryl iodides with amines is reported. The high generality of the reaction in de novo synthesis, late-stage modifications, and cascade processes to access functionalized indolinones and carbazoles underscores the synthetic potential of the presented strategy. Monitoring the reaction with ESI-HRMS and NMR provided strong evidence for the in situ formation of putative high valent Au(III) intermediates.

Process for the preparation of nitro diphenyl amine derivatives

-

, (2008/06/13)

A process for the preparation of nitro-diphenyl amines is disclosed by decarboxylation of a urethane in the presence of a base at an elevated temperature using tetramethylene sulphone as reaction medium is disclosed. The urethane can be one formed by the reaction of a nitrophenol with an aromatic isocyanate.

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