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98735-78-5

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98735-78-5 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 98735-78-5 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 9,8,7,3 and 5 respectively; the second part has 2 digits, 7 and 8 respectively.
Calculate Digit Verification of CAS Registry Number 98735-78:
(7*9)+(6*8)+(5*7)+(4*3)+(3*5)+(2*7)+(1*8)=195
195 % 10 = 5
So 98735-78-5 is a valid CAS Registry Number.

98735-78-5SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 12, 2017

Revision Date: Aug 12, 2017

1.Identification

1.1 GHS Product identifier

Product name (6S)-6-Methyl-4,7-diazaspiro[2.5]octane-5,8-dione

1.2 Other means of identification

Product number -
Other names (S)-6-METHYL-4,7-DIAZASPIRO[2.5]OCTANE-5,8-DIONE

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:98735-78-5 SDS

98735-78-5Upstream product

98735-78-5Downstream Products

98735-78-5Relevant articles and documents

IMIDAZOTHIAZOLE DERIVATIVE HAVING 4,7-DIAZASPIROY2.5¨OCTANE RING STRUCTURE

-

Page/Page column 96-97, (2011/04/18)

There is provided a novel compound that inhibits the interaction between murine double minute 2 (Mdm2) protein and p53 protein and exhibits anti-tumor activity. The present invention provides an imidazothiazole derivative represented by the following formula (1) having various substituents that inhibits the interaction between Mdm2 protein and p53 protein and exhibits anti-tumor activity: wherein R1 R2, R3, R4, R5, Ar1, and Ar2 in formula (1) each have the same meanings as defined in the specification.

Stereochemistry of Cyclic Dipeptides. Assignment of the Prochiral Methylenes of 1-Aminocyclopropane-1-carboxylic Acid

Woodard, Ronald W.

, p. 4796 - 4799 (2007/10/02)

The two enantiomeric methylene carbons of 1-aminocyclopropane-1-carboxylic acid (ACC) were differentiated by an NMR study.Several amino acids such as L-alanine, D-alanine, and 2-aminoisobutyric acid as well as ACC were condensed with L- and/or D-phenylala

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