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1033-34-7

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1033-34-7 Usage

General Description

6-benzyl-2-(methylsulfanyl)-5,6,7,8-tetrahydropyrido[4,3-d]pyrimidin-4(1H)-one is a chemical compound with a complex structure. It contains a benzyl group, a methylsulfanyl group, and a tetrahydropyrido[4,3-d]pyrimidin-4(1H)-one ring system. 6-benzyl-2-(methylsulfanyl)-5,6,7,8-tetrahydropyrido[4,3-d]pyrimidin-4(1H)-one may have potential applications in pharmaceuticals or as a building block for the synthesis of other chemical compounds. Its structural features suggest that it may have biological activity and could be of interest in medicinal chemistry research. Overall, this compound has a unique and complex structure that could make it valuable for various scientific and industrial applications.

Check Digit Verification of cas no

The CAS Registry Mumber 1033-34-7 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 1,0,3 and 3 respectively; the second part has 2 digits, 3 and 4 respectively.
Calculate Digit Verification of CAS Registry Number 1033-34:
(6*1)+(5*0)+(4*3)+(3*3)+(2*3)+(1*4)=37
37 % 10 = 7
So 1033-34-7 is a valid CAS Registry Number.

1033-34-7SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 15, 2017

Revision Date: Aug 15, 2017

1.Identification

1.1 GHS Product identifier

Product name 6-benzyl-2-methylsulfanyl-1,5,7,8-tetrahydropyrido[4,3-d]pyrimidin-4-one

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

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More Details:1033-34-7 SDS

1033-34-7Relevant articles and documents

2-Alkyl-4-oxohexahydropyrimido[4,5-d]- and -[5,4-d]azocines

Voskressensky,Ovcharov,Borisova,Kulikova,Listratova,Borisov,Varlamov

experimental part, p. 222 - 228 (2011/12/15)

It has been established that 2-R-4-oxotetrahydropyrido[4,3-d]pyrimidines, under the action of activated alkynes in methanol, form a mixture of 2-R-4-oxohexahydropyrimido[4,5-d]azocines and products of decomposition of the tetrahydropyridine ring, the 2-R-5-methoxymethyl-4-oxo-6-vinylaminoethyl- pyrimidines. Tetrahydropyrido[3,4-d]pyrimidine, isomeric at the junction of the pyrimidine and tetrahydropyridine rings, forms only the corresponding pyrimido[5,4-d]azocine, the product of expansion, under the action of methyl propiolate.

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