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615-86-1

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615-86-1 Usage

General Description

2,4,5-tribromoaniline is a chemical compound that consists of a benzene ring with three bromine atoms attached to it. It is a derivative of aniline, which is a primary aromatic amine. 2,4,5-tribromoaniline is used in the synthesis of various pharmaceuticals, dyes, and organic compounds. It is also used as an intermediate in the production of agricultural chemicals and as a reagent in organic synthesis. 2,4,5-tribromoaniline is known to be toxic and may cause irritation to the skin, eyes, and respiratory system. Additionally, it may have harmful effects on aquatic organisms and the environment. Therefore, proper handling and disposal of 2,4,5-tribromoaniline are essential to prevent any negative impacts.

Check Digit Verification of cas no

The CAS Registry Mumber 615-86-1 includes 6 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 3 digits, 6,1 and 5 respectively; the second part has 2 digits, 8 and 6 respectively.
Calculate Digit Verification of CAS Registry Number 615-86:
(5*6)+(4*1)+(3*5)+(2*8)+(1*6)=71
71 % 10 = 1
So 615-86-1 is a valid CAS Registry Number.

615-86-1SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 12, 2017

Revision Date: Aug 12, 2017

1.Identification

1.1 GHS Product identifier

Product name 2,4,5-tribromoaniline

1.2 Other means of identification

Product number -
Other names 2,4,5-tribromo-aniline

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:615-86-1 SDS

615-86-1Relevant articles and documents

Synthesis of symmetrical dinitro-and diamino-substituted Troeger's base analogues

Sturala, Jiri,Cibulka, Radek

supporting information, p. 7066 - 7074 (2013/02/21)

This report describes a new synthetic approach to symmetrical diamino-substituted Troeger's base analogues, allowing the synthesis of 1,7-, and 4,10-diamino derivatives with no additional substituents and of 3,9-diamino derivative with methyl groups in the 1-, 4-, 7-and 10-positions. The synthesis uses regioselective nitration of dihalo-substituted-or tetrahalo-substituted Troeger's bases followed either by hydrogenation of the nitro functions accompanied by removal of halogen atoms or alternatively by chemoselective reduction of nitro groups to obtain the dihalo-diamino- substituted Troeger's base analogues. The 2,8-diamino derivatives, not accessible by this approach, can be prepared by Buchwald-Hartwig amination of the 2,8-dibromo-substituted Troeger's bases.

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