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2-(2-(Methylthio)pyrimidin-4-yl)malonaldehyde is an organic compound characterized by its molecular formula C8H8N2O2S. It is a yellow to brown crystalline solid that exhibits unique reactivity due to the presence of a pyrimidine ring and a malonaldehyde moiety. 2-(2-(methylthio)pyrimidin-4-yl)malonaldehyde is utilized in various chemical processes, particularly in the synthesis of pharmaceuticals, agrochemicals, and other fine chemicals.

77168-37-7

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77168-37-7 Usage

Uses

Used in Pharmaceutical Industry:
2-(2-(Methylthio)pyrimidin-4-yl)malonaldehyde is used as a key intermediate in the synthesis of various pharmaceuticals. Its unique chemical structure allows for the development of new drugs with potential therapeutic applications.
Used in Agrochemical Industry:
In the agrochemical industry, 2-(2-(methylthio)pyrimidin-4-yl)malonaldehyde is employed as a precursor in the production of agrochemicals. Its reactivity and chemical properties contribute to the creation of effective compounds for agricultural use.
Used in Organic Synthesis:
2-(2-(Methylthio)pyrimidin-4-yl)malonaldehyde is used as a reagent in organic synthesis, enabling the formation of complex organic molecules. Its versatility in chemical reactions makes it a valuable component in the synthesis of a wide range of organic compounds.
Used in Fine Chemicals Production:
2-(2-(methylthio)pyrimidin-4-yl)malonaldehyde is also utilized in the production of fine chemicals, which are high-purity chemicals used in various industries, including pharmaceuticals, fragrances, and flavors. The unique properties of 2-(2-(methylthio)pyrimidin-4-yl)malonaldehyde contribute to the development of high-quality fine chemicals.
It is crucial to handle and store 2-(2-(methylthio)pyrimidin-4-yl)malonaldehyde with care, as it may pose certain health and safety hazards if not properly managed. Proper handling and storage practices are essential to ensure the safety of individuals working with this chemical and to maintain the integrity of the compounds produced using it.

Check Digit Verification of cas no

The CAS Registry Mumber 77168-37-7 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 7,7,1,6 and 8 respectively; the second part has 2 digits, 3 and 7 respectively.
Calculate Digit Verification of CAS Registry Number 77168-37:
(7*7)+(6*7)+(5*1)+(4*6)+(3*8)+(2*3)+(1*7)=157
157 % 10 = 7
So 77168-37-7 is a valid CAS Registry Number.
InChI:InChI=1/C8H8N2O2S/c1-13-8-9-3-2-7(10-8)6(4-11)5-12/h2-6H,1H3

77168-37-7SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 18, 2017

Revision Date: Aug 18, 2017

1.Identification

1.1 GHS Product identifier

Product name 2-(2-methylsulfanylpyrimidin-4-yl)propanedial

1.2 Other means of identification

Product number -
Other names S03-0164

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:77168-37-7 SDS

77168-37-7Downstream Products

77168-37-7Relevant academic research and scientific papers

Unfused Heterobicycles as Amplifiers of Phleomycin.I Some Pyridinyl- and Pyrazolyl-pyrimidines, Bithiazoles and Thiazolylpyridines

Brown, Desmond J.,Cowden, William B.,Grigg, Geoffrey W.,Kavulak, Diana

, p. 2291 - 2298 (2007/10/02)

Syntheses are reported for some simple derivatives of 2-(pyridin-2'-yl)pyrimidine; 4-(pyrazol-1'-yl)pyrimidine; 4-(pyrazol-4'-yl)pyrimidine; 4,5'-bithiazole; 2-, 3-, and 4-(thiazol-4'-yl)pyridine and 2-, 3-, and 4-(thiazol-2'-yl)pyridine.Biological activities, as amplifiers of phleomycin against in vitro cultures of Escherichia coli, are tabulated and discussed.

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