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1393456-97-7

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1393456-97-7 Usage

Description

(4-Chloro-2-(methylthio)-6-(piperidin-1-yl)pyrimidin-5-yl)(phenyl)methanol is a complex organic molecule with a molecular formula of C19H20ClN3OS. It is a white, crystalline solid that contains various functional groups, including chloro, methylthio, piperidin-1-yl, pyrimidin-yl, and phenyl groups. (4-Chloro-2-(methylthio)-6-(piperidin-1-yl)pyrimidin-5-yl)(phenyl)methanol is of interest in pharmaceutical research and development due to its potential medicinal properties and interactions with biological targets.

Uses

Used in Pharmaceutical Research and Development:
(4-Chloro-2-(methylthio)-6-(piperidin-1-yl)pyrimidin-5-yl)(phenyl)methanol is used as a compound of interest in pharmaceutical research and development for its potential medicinal properties. The presence of the phenyl group suggests that it may have interactions with biological targets, making it a promising candidate for drug discovery.
Used in Central Nervous System Applications:
(4-Chloro-2-(methylthio)-6-(piperidin-1-yl)pyrimidin-5-yl)(phenyl)methanol is used as a compound with potential activity on the central nervous system due to the presence of the piperidin-1-yl group. This characteristic makes it a target for further study and evaluation in the development of therapeutic agents for neurological disorders.
Used in Drug Discovery:
(4-Chloro-2-(methylthio)-6-(piperidin-1-yl)pyrimidin-5-yl)(phenyl)methanol is used as a target for drug discovery, as its complex structure and various functional groups may provide insights into the development of new therapeutic agents with novel mechanisms of action.
Used in Medicinal Chemistry:
(4-Chloro-2-(methylthio)-6-(piperidin-1-yl)pyrimidin-5-yl)(phenyl)methanol is used as a starting point for medicinal chemistry research, where its structure can be modified and optimized to enhance its therapeutic potential and selectivity for specific biological targets.

Check Digit Verification of cas no

The CAS Registry Mumber 1393456-97-7 includes 10 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 7 digits, 1,3,9,3,4,5 and 6 respectively; the second part has 2 digits, 9 and 7 respectively.
Calculate Digit Verification of CAS Registry Number 1393456-97:
(9*1)+(8*3)+(7*9)+(6*3)+(5*4)+(4*5)+(3*6)+(2*9)+(1*7)=197
197 % 10 = 7
So 1393456-97-7 is a valid CAS Registry Number.

1393456-97-7SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 12, 2017

Revision Date: Aug 12, 2017

1.Identification

1.1 GHS Product identifier

Product name (4-chloro-2-methylsulfanyl-6-piperidin-1-ylpyrimidin-5-yl)-phenylmethanol

1.2 Other means of identification

Product number -
Other names (4-Chloro-2-(methylthio)-6-(piperidin-1-yl)pyrimidin-5-yl)(phenyl)methanol

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 -
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More Details:1393456-97-7 SDS

1393456-97-7Relevant articles and documents

Synthesis of 5,6-disubstituted thieno[2,3-d]pyrimidines from 4-chloropyrimidines

Kobayashi, Kazuhiro,Suzuki, Teruhiko,Kozuki, Taketoshi,Matsumoto, Naoki,Hiyoshi, Hidetaka,Umezu, Kazuto

experimental part, p. 1405 - 1416 (2012/08/07)

Facile reaction sequences for the preparation of 5,6-disubstituted thieno[2,3-d]pyrimidines starting with 4-chloropyrimidines have been developed. 4-Chloro-6-methoxypyrimidines were aroylated at the 5-positions via lithiation with LDA and subsequent treatment with benzaldehyde or N-methoxy- Nmethylbenzamides to give aryl(4-chloro-6-methoxypyrimidin-5-yl)methanones. These pyrimidinyl ketones were transformed in one-pot into 5,6-disubstituted 4-methoxythieno[2,3-d]pyrimidines by a successive treatment with sodium sulfide, BrCH2EWGs, and sodium hydride. Lithiation of 4,6-dichloro-2-(methylsulfanyl) pyrimidine at the 5-position was followed by treatment with tertiary formamides to give 4-chloro-6-(dialkylamino)pyrimidine-5-carboxaldehydes, which could be transformed into 5,6-disubstituted 4-(dialkylamino)thieno[2,3-d]pyrimidines via aryl[4-chloro-6-(dialkylamino)-pyrimidin-5-yl]methanones using the same one-pot thiophene ring forming sequence.

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