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774238-90-3

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774238-90-3 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 774238-90-3 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 7,7,4,2,3 and 8 respectively; the second part has 2 digits, 9 and 0 respectively.
Calculate Digit Verification of CAS Registry Number 774238-90:
(8*7)+(7*7)+(6*4)+(5*2)+(4*3)+(3*8)+(2*9)+(1*0)=193
193 % 10 = 3
So 774238-90-3 is a valid CAS Registry Number.

774238-90-3SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 19, 2017

Revision Date: Aug 19, 2017

1.Identification

1.1 GHS Product identifier

Product name tert-butyl N-[[4-(hydroxymethyl)phenyl]methyl]-N-methylcarbamate

1.2 Other means of identification

Product number -
Other names -

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:774238-90-3 SDS

774238-90-3Relevant articles and documents

IRAK DEGRADERS AND USES THEREOF

-

, (2020/06/19)

The present invention provides compounds, compositions thereof, and methods of using the same.

PROBES FOR IMAGING HUNTINGTIN PROTEIN

-

, (2016/03/22)

Provided are imaging agents comprising a compound of Formula (I), or a pharmaceutically acceptable salt thereof, and methods of their use.

Discovery of novel thieno[2,3-d]pyrimidin-4-yl hydrazone-based inhibitors of Cyclin D1-CDK4: Synthesis, biological evaluation and structure-activity relationships. Part 2

Horiuchi, Takao,Nagata, Motoko,Kitagawa, Mayumi,Akahane, Kouichi,Uoto, Kouichi

experimental part, p. 7850 - 7860 (2010/04/02)

The design, synthesis and evaluation of novel thieno[2,3-d]pyrimidin-4-yl hydrazone analogues as cyclin-dependent kinase 4 (CDK4) inhibitor are described. Focusing on the optimization of the heteroaryl moiety at the hydrazone with substituted phenyl group

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