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7632-73-7

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7632-73-7 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 7632-73-7 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 7,6,3 and 2 respectively; the second part has 2 digits, 7 and 3 respectively.
Calculate Digit Verification of CAS Registry Number 7632-73:
(6*7)+(5*6)+(4*3)+(3*2)+(2*7)+(1*3)=107
107 % 10 = 7
So 7632-73-7 is a valid CAS Registry Number.

7632-73-7SDS

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 1-phenyl-3-piperidin-1-ylprop-2-ene-1-thione

1.2 Other means of identification

Product number -
Other names 1-phenyl-3-piperidin-1-yl-prop-2-ene-1-thione

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:7632-73-7 SDS

7632-73-7Relevant articles and documents

IMINE CHEMISTRY-II.A NEW ROUTE TO CYCLIC ENAMINONES FROM IMINES AND β-PROPIOLACTONE OR α,β-UNSATURATED ACIDS. THE PREPARATION OF ENAMINO-THIONES

Shabana, R.,Rasmussen, J. B.,Olesen, S. O.,Lawesson, S.-O.

, p. 3047 - 3051 (2007/10/02)

Imines, formed from cyclohexanone and primary aromatic and aliphatic amines, were reacted with β-propiolactone, acrylic, crotonic, and methacrylic acids to give as main products bicyclic lactams, 3,4,5,6,7,8-hexahydro-2-quinolinone, 2, and enaminones, 2,3,5,6,7,8-hexahydro-4-quinolinone, 3.The enaminones 3 and a series of noncyclic enaminones 11 were reacted with 2,4-bis(4-methoxyphenyl)-1,3,2,4-dithiadiphosphetane-2,4-disulfide, 9, a new thiation reagent, giving the corresponding enamino-thiones 10 and 12, respectively.Compound 2a was also reacted with 9 giving N-phenyl- 3,4,5,6,7,8-hexahydro-2-quinolinthione, 13a. 360 MHz (1)H NMR and 90.25 MHz (13)C NMR data are reported for the compounds 2a, 3a and 10a.

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