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CAS

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75712-73-1

Pyrimidine, 5-chloro-2,4-dimethyl- (9CI) is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

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  • 75712-73-1 Structure

  • Basic information

    1. Product Name: Pyrimidine, 5-chloro-2,4-dimethyl- (9CI)
    2. Synonyms: Pyrimidine, 5-chloro-2,4-dimethyl- (9CI);5-Chloro-2,4-diMethylpyriMidine
    3. CAS NO:75712-73-1
    4. Molecular Formula: C6H7ClN2
    5. Molecular Weight: 142.58618
    6. EINECS: N/A
    7. Product Categories: PYRIMIDINE
    8. Mol File: 75712-73-1.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.: 2-8°C
    8. Solubility: N/A
    9. CAS DataBase Reference: Pyrimidine, 5-chloro-2,4-dimethyl- (9CI)(CAS DataBase Reference)
    10. NIST Chemistry Reference: Pyrimidine, 5-chloro-2,4-dimethyl- (9CI)(75712-73-1)
    11. EPA Substance Registry System: Pyrimidine, 5-chloro-2,4-dimethyl- (9CI)(75712-73-1)

  • 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: 75712-73-1(Hazardous Substances Data)

75712-73-1 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 75712-73-1 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 7,5,7,1 and 2 respectively; the second part has 2 digits, 7 and 3 respectively.
Calculate Digit Verification of CAS Registry Number 75712-73:
(7*7)+(6*5)+(5*7)+(4*1)+(3*2)+(2*7)+(1*3)=141
141 % 10 = 1
So 75712-73-1 is a valid CAS Registry Number.

75712-73-1SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 20, 2017

Revision Date: Aug 20, 2017

1.Identification

1.1 GHS Product identifier

Product name 5-chloro-2,4-dimethylpyrimidine

1.2 Other means of identification

Product number -
Other names Pyrimidine,5-chloro-2,4-dimethyl

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:75712-73-1 SDS

75712-73-1Downstream Products

75712-73-1Relevant articles and documents

SUBSTITUTED CYCLOPROPYL COMPOUNDS, COMPOSITIONS CONTAINING SUCH COMPOUNDS AND METHODS OF TREATMENT

-

Page/Page column 80-81, (2009/12/02)

Substituted cyclopropyl compounds of formula (I) are disclosed as useful for treating or preventing type 2 diabetes and similar conditions. Pharmaceutically acceptable salts and solvates are included as well. The compounds are useful as agonists of the g-protein coupled receptor GPR-119.

Reactions of Halogenomethanes in the Vapor Phase. Part 4. The Reactions of Imidazoles with Chloroform at 550 deg C, and a Comparison with their Liquid-phase Reactions with Trichloroacetate Ion or Hexachloroacetone and Base

Busby, Reginald E.,Khan, Mohammad A.,Khan, Mohammad R.,Parrick, John,Shaw, C. J. Granville,Iqbal, Mohammad

, p. 1427 - 1430 (2007/10/02)

1-Unsubstituted imidazoles and chloroform at 550 deg C in a flow system give mainly 5-chloropyrimidines, together with 4-chloropyrimidines and chloropyrazines.The effects of methyl substituents on the ratio of products is considered.The liquid-phase reactions of 2-methyl- and 2,4,5-trimethyl-imidazole under conditions in which dichlorocarbene is said to be formed in basic or neutral conditions were studied, and compared with the gas-phase reactions with chloroform.

Reactions of Halogenomethanes in the Vapour Phase. Part 5. The Reactions of Imidazolines, Anils, and 1-Methylimidazole with Chloroform at 550 deg C, and a Comparison with their Liquid-Phase Reactions with Trichloroacetate Ion or Hexachloroacetone and Base

Busby, Reginald E.,Khan, Mohammad A.,Khan, Mohammad R.,Parrick, John,Shaw, C. J. Granville

, p. 1431 - 1435 (2007/10/02)

The vapor-phase reactions of imidazolines and anils with chloroform at 550 deg C are compared with their liquid-phase reactions in the presence of hexachloroacetone and base or upon thermolysis with trichloroacetate ion.In the vapour-phase reactions imidazolines, unlike imidazoles, gave non-chlorinated pyrimidines, and 1-methyl-imidazole gave 2-cyanopyrrole and the four 3-chlorocyanopyridines.

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