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5007-36-3

5007-36-3

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5007-36-3 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 5007-36-3 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 5,0,0 and 7 respectively; the second part has 2 digits, 3 and 6 respectively.
Calculate Digit Verification of CAS Registry Number 5007-36:
(6*5)+(5*0)+(4*0)+(3*7)+(2*3)+(1*6)=63
63 % 10 = 3
So 5007-36-3 is a valid CAS Registry Number.

5007-36-3SDS

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 6-phenyl-1,3-diazaspiro[4.5]decane-2,4-dione

1.2 Other means of identification

Product number -
Other names 10-phenyl-2,4-diazaspiro[4.5]decane-1,3-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:5007-36-3 SDS

5007-36-3Relevant articles and documents

New spirohydantoin derivatives - Synthesis, pharmacological evaluation, and molecular modeling study

Czopek, Anna,Zagórska, Agnieszka,Ko?aczkowski, Marcin,Bucki, Adam,Gryz?o, Beata,Rychtyk, Joanna,Paw?owski, Maciej,Siwek, Agata,Sata?a, Grzegorz,Bojarski, Andrzej,Kubacka, Monika,Filipek, Barbara

, p. 1545 - 1554 (2016/12/18)

A series of new arylpiperazinylpropyl derivatives of 8/6-phenyl-1,3-diazaspiro[4.5]decan-2,4-dione and spiro[imidazolidine-4,1′-indene/naphthalene]-2,5-dione was synthesized and their affinity was evaluated toward serotonin 5-HT1A, 5-HT2A

Stereochemistry of the conventional and modified Bucherer-Bergs reactions of 2-substituted cyclohexanones

Sacripante, Guerino,Edward, John T.

, p. 1982 - 1987 (2007/10/02)

The configurations of the spiro-hydantoins produced from 2-methyl- and 2-phenylcyclohexanone, 2,6-dimethylcyclohexanone, and dl-menthone by either the conventional Bucherer-Bergs (B.-B.) reaction, or a variant employing COS or CS2 in place of C

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