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914636-84-3

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914636-84-3 Usage

Properties

Nitrile derivative with a substituted benzene ring containing bromine, chlorine, and amino groups
Used in pharmaceutical and agrochemical industries as an intermediate for synthesis of various organic molecules and active pharmaceutical ingredients
Utilized in research and development for creation of new drugs and agrochemicals
Potential applications in material science and chemical synthesis due to unique chemical properties and reactivity

Usage

Intermediate for synthesis in pharmaceutical and agrochemical industries

Applications

Research and development, material science, chemical synthesis

Check Digit Verification of cas no

The CAS Registry Mumber 914636-84-3 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 9,1,4,6,3 and 6 respectively; the second part has 2 digits, 8 and 4 respectively.
Calculate Digit Verification of CAS Registry Number 914636-84:
(8*9)+(7*1)+(6*4)+(5*6)+(4*3)+(3*6)+(2*8)+(1*4)=183
183 % 10 = 3
So 914636-84-3 is a valid CAS Registry Number.

914636-84-3SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 18, 2017

Revision Date: Aug 18, 2017

1.Identification

1.1 GHS Product identifier

Product name 2-Amino-3-bromo-5-chlorobenzonitrile

1.2 Other means of identification

Product number -
Other names OR6760

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:914636-84-3 SDS

914636-84-3Relevant articles and documents

A PROCESS FOR THE SYNTHESIS ANTHRANILIC DIAMIDE COMPOUNDS AND INTERMEDIATES THEREOF

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Page/Page column 21; 22, (2020/09/08)

The present invention disclosed a process for the synthesis of anthranilic diamide compound of formula (I), wherein, R1, R2, R3a, R3b, R3c, R4, R5, R6 and Z are as defined in the detailed description. The process comprising the step of obtaining a mono- or dicyano substituted aniline compound of formula (IV) which is then converted to an anthranilic acid compound of formula (V) or an anthranilic amide compound of formula (Va). Further, the compound of formula (VI) can be optionally synthesized from compound of formula (IV or V or Va).

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