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126926-34-9

126926-34-9

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126926-34-9 Usage

Uses

3-(Hydroxymethyl)Benzamide (~85%) can be used as HDAC8 inhibitors.

Check Digit Verification of cas no

The CAS Registry Mumber 126926-34-9 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,2,6,9,2 and 6 respectively; the second part has 2 digits, 3 and 4 respectively.
Calculate Digit Verification of CAS Registry Number 126926-34:
(8*1)+(7*2)+(6*6)+(5*9)+(4*2)+(3*6)+(2*3)+(1*4)=139
139 % 10 = 9
So 126926-34-9 is a valid CAS Registry Number.
InChI:InChI=1/C8H9NO2/c9-8(11)7-3-1-2-6(4-7)5-10/h1-4,10H,5H2,(H2,9,11)

126926-34-9SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 19, 2017

Revision Date: Aug 19, 2017

1.Identification

1.1 GHS Product identifier

Product name 3-(Hydroxymethyl)benzamide

1.2 Other means of identification

Product number -
Other names 3-Hydroxymethylbenzamide

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:126926-34-9 SDS

126926-34-9Upstream product

126926-34-9Downstream Products

126926-34-9Relevant articles and documents

Transition metal-free sodium borohydride promoted controlled hydration of nitriles to amides

Verma, Praveen Kumar,Kumar, Neeraj,Sharma, Upendra,Bala, Manju,Kumar, Vishal,Singh, Bikram

, p. 2867 - 2875 (2013/09/02)

A transition metal-free process, promoted by sodium borohydride, has been developed for convenient and selective hydration of nitriles to corresponding amides. The present process converts the aromatic, aliphatic, and heteroaromatic nitriles with wide functional group tolerance. The regioselective hydration of one nitrile moiety in the presence of an other nitrile group makes high impact in the present protocol.

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