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1229383-37-2

7-aMinoiMidazo[1,2,c]pyriMidine is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

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  • 1229383-37-2 Structure

  • Basic information

    1. Product Name: 7-aMinoiMidazo[1,2,c]pyriMidine
    2. Synonyms: 7-aMinoiMidazo[1,2,c]pyriMidine;imidazo[1,2-c]pyrimidin-7-amine
    3. CAS NO:1229383-37-2
    4. Molecular Formula: C6H6N4
    5. Molecular Weight: 134.13864
    6. EINECS: -0
    7. Product Categories: organic building block
    8. Mol File: 1229383-37-2.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.: Keep in dark place,Sealed in dry,Room Temperature
    8. Solubility: N/A
    9. CAS DataBase Reference: 7-aMinoiMidazo[1,2,c]pyriMidine(CAS DataBase Reference)
    10. NIST Chemistry Reference: 7-aMinoiMidazo[1,2,c]pyriMidine(1229383-37-2)
    11. EPA Substance Registry System: 7-aMinoiMidazo[1,2,c]pyriMidine(1229383-37-2)

  • 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: 1229383-37-2(Hazardous Substances Data)

1229383-37-2 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 1229383-37-2 includes 10 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 7 digits, 1,2,2,9,3,8 and 3 respectively; the second part has 2 digits, 3 and 7 respectively.
Calculate Digit Verification of CAS Registry Number 1229383-37:
(9*1)+(8*2)+(7*2)+(6*9)+(5*3)+(4*8)+(3*3)+(2*3)+(1*7)=162
162 % 10 = 2
So 1229383-37-2 is a valid CAS Registry Number.

1229383-37-2SDS

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 imidazo[1,2-c]pyrimidin-7-ylamine

1.2 Other means of identification

Product number -
Other names Imidazo[1,2-c]pyrimidin-7-amine

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:1229383-37-2 SDS

1229383-37-2Downstream Products

1229383-37-2Relevant articles and documents

Heteroaryl urea inhibitors of fatty acid amide hydrolase: Structure-mutagenicity relationships for arylamine metabolites

Tichenor, Mark S.,Keith, John M.,Jones, William M.,Pierce, Joan M.,Merit, Jeff,Hawryluk, Natalie,Seierstad, Mark,Palmer, James A.,Webb, Michael,Karbarz, Mark J.,Wilson, Sandy J.,Wennerholm, Michelle L.,Woestenborghs, Filip,Beerens, Dominiek,Luo, Lin,Brown, Sean M.,Boeck, Marlies De,Chaplan, Sandra R.,Breitenbucher, J. Guy

, p. 7357 - 7362 (2013/02/21)

The structure-activity relationships for a series of heteroaryl urea inhibitors of fatty acid amide hydrolase (FAAH) are described. Members of this class of inhibitors have been shown to inactivate FAAH by covalent modification of an active site serine with subsequent release of an aromatic amine from the urea electrophile. Systematic Ames II testing guided the optimization of urea substituents by defining the structure-mutagenicity relationships for the released aromatic amine metabolites. Potent FAAH inhibitors were identified having heteroaryl amine leaving groups that were non-mutagenic in the Ames II assay.

HETEROARYL-SUBSTITUTED UREA MODULATORS OF FATTY ACID AMIDE HYDROLASE

-

Page/Page column 29, (2010/07/02)

Certain heteroaryl-substituted piperidinyl and piperazinyl urea compounds are described, which are useful as FAAH inhibitors. Such compounds may be used in pharmaceutical compositions and methods for the treatment of disease states, disorders, and conditions mediated by fatty acid amide hydrolase (FAAH) activity, such as anxiety, pain, inflammation, sleep disorders, eating disorders, insulin resistance, diabetes, osteoporosis, and movement disorders (e.g., multiple sclerosis).

HETEROARYL-SUBSTITUTED UREA MODULATORS OF FATTY ACID AMIDE HYDROLASE

-

Page/Page column 33, (2010/07/02)

Certain heteroaryl-substituted piperidinyl and piperazinyl urea compounds are described, which are useful as FAAH inhibitors. Such compounds may be used in pharmaceutical compositions and methods for the treatment of disease states, disorders, and conditions mediated by fatty acid amide hydrolase (FAAH) activity, such as anxiety, pain, inflammation, sleep disorders, eating disorders, insulin resistance, diabetes, osteoporosis, and movement disorders (e.g., multiple sclerosis).

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