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Check Digit Verification of cas no

The CAS Registry Mumber 656803-51-9 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 6,5,6,8,0 and 3 respectively; the second part has 2 digits, 5 and 1 respectively.
Calculate Digit Verification of CAS Registry Number 656803-51:
(8*6)+(7*5)+(6*6)+(5*8)+(4*0)+(3*3)+(2*5)+(1*1)=179
179 % 10 = 9
So 656803-51-9 is a valid CAS Registry Number.

656803-51-9SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 13, 2017

Revision Date: Aug 13, 2017

1.Identification

1.1 GHS Product identifier

Product name	tert-butyl 4-(3-methoxy-3-oxopropyl)piperazine-1-carboxylate

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:656803-51-9 SDS

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656803-51-9Relevant articles and documents

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Paragraph 0086-0088, (2019/08/20)

The invention discloses pyrimidopyridone compounds having antitumor activity as well as a preparation method and application of the pyrimidopyridone compounds. The invention particularly discloses thedeuterated pyrimidopyridone compounds represented by a

NEW ANTIBACTERIAL COMPOUNDS

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Page/Page column 59-60, (2016/07/05)

The present invention relates to novel antibacterial compounds, pharmaceutical compositions containing them and their use as antimicrobials.

Design and synthesis of novel sulfonamide-containing bradykinin hB 2 receptor antagonists. Synthesis and structure-relationships of α,α-tetrahydropyranylglycine

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supporting information; experimental part, p. 2091 - 2100 (2012/05/05)

A series of α,α-cycloalkylglycine sulfonamide compounds of general formula 1 has previously been identified by our group as selective human B2(hB2) receptor antagonists. Here we report the in vitro and in vivo BK antagonist activity

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656803-51-9