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40718-08-9

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40718-08-9 Usage

General Description

3,5-Dibromo-2-hydroxybenzonitrile is a chemical compound with the molecular formula C7H3Br2NO. It is a white to light yellow crystalline solid that is commonly used as an intermediate in the synthesis of pharmaceuticals, agrochemicals, and dyes. 3,5-DIBROMO-2-HYDROXYBENZONITRILE is known for its strong antimicrobial and antifungal properties, making it useful in the development of new medications and pesticides. Additionally, it is used as a building block in the production of various organic compounds due to its ability to undergo various chemical reactions, such as nucleophilic substitution and aromatic bromination. Overall, 3,5-Dibromo-2-hydroxybenzonitrile is a versatile chemical with a range of industrial applications.

Check Digit Verification of cas no

The CAS Registry Mumber 40718-08-9 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 4,0,7,1 and 8 respectively; the second part has 2 digits, 0 and 8 respectively.
Calculate Digit Verification of CAS Registry Number 40718-08:
(7*4)+(6*0)+(5*7)+(4*1)+(3*8)+(2*0)+(1*8)=99
99 % 10 = 9
So 40718-08-9 is a valid CAS Registry Number.
InChI:InChI=1/C7H3Br2NO/c8-5-1-4(3-10)7(11)6(9)2-5/h1-2,11H

40718-08-9SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 20, 2017

Revision Date: Aug 20, 2017

1.Identification

1.1 GHS Product identifier

Product name 3,5-DIBROMO-2-HYDROXYBENZONITRILE

1.2 Other means of identification

Product number -
Other names 3,5-dibromo-2-hydroxy-benzonitrile

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:40718-08-9 SDS

40718-08-9Relevant articles and documents

Chromatography-free entry to substituted salicylonitriles: Mitsunobu-triggered domino reactions of salicylaldoximes

Whiting, Ellis,Lanning, Maryanna E.,Scheenstra, Jacob A.,Fletcher, Steven

, p. 1229 - 1234 (2015/01/30)

A mild and efficient one-pot procedure is described to transform salicylaldoximes into salicylonitriles using Mitsunobu chemistry. The reactions proceed through the corresponding 1,2-benzisoxazoles that undergo the Kemp elimination in situ to generate the

A New Bromination Method for Phenols and Anisoles: NBS/HBF4*Et2O in CH3CN

Oberhauser, Thomas

, p. 4504 - 4506 (2007/10/03)

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