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2-Thiophenecarboxylicacid,3-amino-5-(1-methylethyl)-,methylester(9CI) is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

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  • 2-Thiophenecarboxylicacid,3-amino-5-(1-methylethyl)-,methylester(9CI)

    Cas No: 216574-44-6

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  • 216574-44-6 Structure
  • Basic information

    1. Product Name: 2-Thiophenecarboxylicacid,3-amino-5-(1-methylethyl)-,methylester(9CI)
    2. Synonyms: 2-Thiophenecarboxylicacid,3-amino-5-(1-methylethyl)-,methylester(9CI);Methyl 3-amino-5-(propan-2-yl)thiophene-2-carboxylate
    3. CAS NO:216574-44-6
    4. Molecular Formula: C9H13NO2S
    5. Molecular Weight: 199.27
    6. EINECS: N/A
    7. Product Categories: AMINOACID
    8. Mol File: 216574-44-6.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.: N/A
    8. Solubility: N/A
    9. CAS DataBase Reference: 2-Thiophenecarboxylicacid,3-amino-5-(1-methylethyl)-,methylester(9CI)(CAS DataBase Reference)
    10. NIST Chemistry Reference: 2-Thiophenecarboxylicacid,3-amino-5-(1-methylethyl)-,methylester(9CI)(216574-44-6)
    11. EPA Substance Registry System: 2-Thiophenecarboxylicacid,3-amino-5-(1-methylethyl)-,methylester(9CI)(216574-44-6)
  • 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: 216574-44-6(Hazardous Substances Data)

216574-44-6 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 216574-44-6 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 2,1,6,5,7 and 4 respectively; the second part has 2 digits, 4 and 4 respectively.
Calculate Digit Verification of CAS Registry Number 216574-44:
(8*2)+(7*1)+(6*6)+(5*5)+(4*7)+(3*4)+(2*4)+(1*4)=136
136 % 10 = 6
So 216574-44-6 is a valid CAS Registry Number.

216574-44-6SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 17, 2017

Revision Date: Aug 17, 2017

1.Identification

1.1 GHS Product identifier

Product name methyl 3-amino-5-propan-2-ylthiophene-2-carboxylate

1.2 Other means of identification

Product number -
Other names 2-thiophenecarboxylic acid,3-amino-5-(1-methylethyl)-,methyl ester

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:216574-44-6 SDS

216574-44-6Downstream Products

216574-44-6Relevant articles and documents

RAF KINASE INHIBITORS

-

Page/Page column 17, (2008/12/06)

Methods of treating tumors mediated by raf kinase, with substituted urea compounds, and such compounds per se.

Inhibition of p38 kinase activity by aryl ureas

-

, (2008/06/13)

This invention relates to the use of a group of aryl ureas in treating cytokine mediated diseases other than cancer and proteolytic enzyme mediated diseases other than cancer, and pharmaceutical compositions for use in such therapy.

p38 kinase inhibitors for the treatment of arthritis and osteoporosis: Thienyl, furyl, and pyrrolyl ureas

Redman, Aniko M,Johnson, Jeffrey S.,Dally, Robert,Swartz, Steve,Wild, Hanno,Paulsen, Holger,Caringal, Yolanda,Gunn, David,Renick, Joel,Osterhout, Martin,Kingery-Wood, Jill,Smith, Roger A.,Lee, Wendy,Dumas, Jacques,Wilhelm, Scott M.,Housley, Timothy J.,Bhargava, Ajay,Ranges, Gerald E.,Shrikhande, Alka,Young, Deborah,Bombara, Michael,Scott, William J.

, p. 9 - 12 (2007/10/03)

Inhibitors of the MAP kinase p38 are potentially useful for the treatment for osteoporosis, arthritis, and other inflammatory diseases. A series of thienyl, furyl, and pyrrolyl ureas has been identified as potent p38 inhibitors, displaying in vitro activity in the nanomolar range. (C) 2000 Elsevier Science Ltd.

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