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1208170-17-5

4-Chloro-6-Methyl-2-(Methylthio)pyrimidine-5-carbonitrile is a complex organic compound that belongs to the pyrimidines family, which are aromatic heterocyclic organic compounds. It is characterized by the presence of chlorine, methyl, methylthio functional groups, and a carbonitrile group in its molecular structure. Although specific details about its properties or common uses are not widely available, it is likely to be used in pharmaceuticals and in the synthesis of more complex organic molecules. Due to potential unknown toxicity or dangerous reactions, it is essential to handle this compound under scientific guidance.

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  • 1208170-17-5 Structure

  • Basic information

    1. Product Name: 4-Chloro-6-Methyl-2-(Methylthio)pyriMidine-5-carbonitrile
    2. Synonyms: 4-Chloro-6-Methyl-2-(Methylthio)pyriMidine-5-carbonitrile
    3. CAS NO:1208170-17-5
    4. Molecular Formula: C7H6ClN3S
    5. Molecular Weight: 199.66064
    6. EINECS: N/A
    7. Product Categories: N/A
    8. Mol File: 1208170-17-5.mol

  • Chemical Properties

    1. Melting Point: N/A
    2. Boiling Point: N/A
    3. Flash Point: N/A
    4. Appearance: /
    5. Density: N/A
    6. Refractive Index: N/A
    7. Storage Temp.: under inert gas (nitrogen or Argon) at 2-8°C
    8. Solubility: N/A
    9. CAS DataBase Reference: 4-Chloro-6-Methyl-2-(Methylthio)pyriMidine-5-carbonitrile(CAS DataBase Reference)
    10. NIST Chemistry Reference: 4-Chloro-6-Methyl-2-(Methylthio)pyriMidine-5-carbonitrile(1208170-17-5)
    11. EPA Substance Registry System: 4-Chloro-6-Methyl-2-(Methylthio)pyriMidine-5-carbonitrile(1208170-17-5)

  • Safety Data

    1. Hazard Codes: N/A
    2. Statements: N/A
    3. Safety Statements: N/A
    4. WGK Germany:
    5. RTECS:
    6. HazardClass: N/A
    7. PackingGroup: N/A
    8. Hazardous Substances Data: 1208170-17-5(Hazardous Substances Data)

1208170-17-5 Usage

Uses

Used in Pharmaceutical Industry:
4-Chloro-6-Methyl-2-(Methylthio)pyrimidine-5-carbonitrile is used as a chemical intermediate for the synthesis of various pharmaceutical compounds. Its unique molecular structure with functional groups such as chlorine, methyl, and methylthio, along with a carbonitrile group, makes it a promising candidate for the development of new drugs.
Used in Organic Synthesis:
4-Chloro-6-Methyl-2-(Methylthio)pyrimidine-5-carbonitrile is used as a building block in the synthesis of more complex organic molecules. Its versatile molecular structure allows for further chemical reactions and modifications, making it a valuable component in the creation of advanced organic compounds for various applications.

Check Digit Verification of cas no

The CAS Registry Mumber 1208170-17-5 includes 10 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 7 digits, 1,2,0,8,1,7 and 0 respectively; the second part has 2 digits, 1 and 7 respectively.
Calculate Digit Verification of CAS Registry Number 1208170-17:
(9*1)+(8*2)+(7*0)+(6*8)+(5*1)+(4*7)+(3*0)+(2*1)+(1*7)=115
115 % 10 = 5
So 1208170-17-5 is a valid CAS Registry Number.

1208170-17-5SDS

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 4-chloro-6-methyl-2-(methylthio)pyrimidine-5-carbonitrile

1.2 Other means of identification

Product number -
Other names 4-chloro-6-methyl-2-(methylthio)-5-pyrimidinecarbonitrile

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:1208170-17-5 SDS

1208170-17-5Relevant articles and documents

Design, synthesis, and antihypertensive activity of new pyrimidine derivatives endowing new pharmacophores

Farghaly, Ahmed M.,AboulWafa, Omaima M.,Elshaier, Yaseen A. M.,Badawi, Waleed A.,Haridy, Haridy H.,Mubarak, Heba A. E.

, p. 360 - 379 (2019)

A new series of achiral pyrimidine derivatives based on nifedipine-like structure was designed and synthesized. These pyrimidyl derivatives contained hydrazine, hydrazones, acetohydrazide, differently substituted benzylidene functionalities, benzosulfohyd

An efficient and practical synthesis of 2,4-substituted pyrido[4,3-d]pyrimidin-5(6H)-ones

Tian, Xinrong,Suarez, Dominic P.,Li, William Hoi Hong,McSherry, Allison K.,Sanchez, Robert M.,Moore, Michael L.,Axten, Jeffrey M.

, (2019/11/13)

We describe an efficient synthesis of 2,4-substituted pyrido[4,3-d]pyrimidin-5(6H)-ones, which involves the acid-promoted cyclization of cyano enamine 15 to afford 2,4-bis(methylthio)pyrido[4,3-d]pyrimidin-5(6H)-one 17 as a key intermediate. Selective displacement of the 4-methylthio group by a wide range of anilines followed by oxidation of the 2-methylthio group and subsequent substitution by amines enabled the synthesis of a variety of 2,4-disubstituted pyrido[4,3-d]pyrimidin-5(6H)-ones.

BICYCLIC INHIBITORS OF ALK

-

, (2014/06/25)

The present invention relates to compounds of formula (1) or pharmaceutical acceptable salts, Formula (1) wherein R1, R2, R3, X, Y, Z, A, B, G1, m, and n are defined in the description. The present invention relates also to compositions containing said compounds which are useful for inhibiting kinases such as ALK and methods of treating diseases such as cancer.

BICYCLIC INHIBITORS OF ALK

-

, (2012/08/07)

The present invention relates to compounds of formula (1) or pharmaceutical acceptable salts, Formula (1) wherein R1, R2, R3, X, Y, Z, A, B, G1, m, and n are defined in the description. The present invention relates also to compositions containing said compounds which are useful for inhibiting kinases such as ALK and methods of treating diseases such as cancer.

CHEMICAL COMPOUNDS

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Page/Page column 55, (2010/04/03)

The invention is directed to pyrido[4,3-d]pyrimidin-5(6H)-one derivatives. Specifically, the invention is directed to compounds according to Formula (I) wherein R1, R2, R3, and R4 are defined below. The compound

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