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757965-23-4

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757965-23-4 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 757965-23-4 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 7,5,7,9,6 and 5 respectively; the second part has 2 digits, 2 and 3 respectively.
Calculate Digit Verification of CAS Registry Number 757965-23:
(8*7)+(7*5)+(6*7)+(5*9)+(4*6)+(3*5)+(2*2)+(1*3)=224
224 % 10 = 4
So 757965-23-4 is a valid CAS Registry Number.

757965-23-4SDS

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 4-O-acetylbenzaldehyde oxime

1.2 Other means of identification

Product number -
Other names 4-acetoxy-benzaldehyde-oxime

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:757965-23-4 SDS

757965-23-4Relevant articles and documents

Synthesis and anti-inflammatory activity of aromatic glucosinolates

Vo, Quan V.,Trenerry, Craige,Rochfort, Simone,Wadeson, Jenny,Leyton, Carolina,Hughes, Andrew B.

, p. 5945 - 5954 (2013/09/23)

Aromatic GLs are important members of the glucosinolate family of compounds because of their potential biological activity and medicinal properties. This study has shown success in the high yielding synthesis of some important aromatic GLs as well as the results of testing for anti-inflammatory properties of the synthetic GLs. 3,4-Dimethoxyphenylglucosinolate was found to be the most active anti-inflammatory of the seven glucosinolates assayed.

A new one pot method for the conversion of aldehydes into nitriles using hydroxyamine and phthalic anhydride

Wang, Eng-Chi,Lin, Gow-Juin

, p. 4047 - 4050 (2007/10/03)

The aryl and alkyl aldehydes were readily converted to give the corresponding nitrites in good yields using hydroxyamine and phthalic anhydride as reagents in one pot.

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