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5-chloro-2-Thiopheneacetic acid is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

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  • 13669-19-7 Structure
  • Basic information

    1. Product Name: 5-chloro-2-Thiopheneacetic acid
    2. Synonyms: 5-chloro-2-Thiopheneacetic acid
    3. CAS NO:13669-19-7
    4. Molecular Formula: C6H5ClO2S
    5. Molecular Weight: 176.62
    6. EINECS: N/A
    7. Product Categories: N/A
    8. Mol File: 13669-19-7.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: 5-chloro-2-Thiopheneacetic acid(CAS DataBase Reference)
    10. NIST Chemistry Reference: 5-chloro-2-Thiopheneacetic acid(13669-19-7)
    11. EPA Substance Registry System: 5-chloro-2-Thiopheneacetic acid(13669-19-7)
  • 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: 13669-19-7(Hazardous Substances Data)

13669-19-7 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 13669-19-7 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 1,3,6,6 and 9 respectively; the second part has 2 digits, 1 and 9 respectively.
Calculate Digit Verification of CAS Registry Number 13669-19:
(7*1)+(6*3)+(5*6)+(4*6)+(3*9)+(2*1)+(1*9)=117
117 % 10 = 7
So 13669-19-7 is a valid CAS Registry Number.

13669-19-7SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 19, 2017

Revision Date: Aug 19, 2017

1.Identification

1.1 GHS Product identifier

Product name 2-(5-chlorothiophen-2-yl)acetic acid

1.2 Other means of identification

Product number -
Other names (5-chlorothiophen-2-yl)acetic acid

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:13669-19-7 SDS

13669-19-7Relevant articles and documents

PYRIDINOPYRIDINONE DERIVATIVES, PREPARATION THEREOF AND THERAPEUTIC USE THEREOF

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Page/Page column 20, (2011/06/19)

The present invention relates to pyridopyridone derivatives of formula (I): in which the variables are as defined herein, to their preparation and to their therapeutic use as inhibitors of the kinase activity of PDGF (platelet-derived growth factor) ligand receptors and possibly of FLT3 (fms-like tyrosine kinase receptor) ligand receptors.

Heterocyclic cycloalkanol ethylamines as norepinephrine reuptake inhibitors

Sabatucci, Joseph P.,Mahaney, Paige E.,Leiter, Jennifer,Johnston, Grace,Burroughs, Kevin,Cosmi, Scott,Zhang, Yingru,Ho, Douglas,Deecher, Darlene C.,Trybulski, Eugene

scheme or table, p. 2809 - 2812 (2010/08/21)

A series of heterocyclic cycloalkanol ethylamines have been prepared to expand our norepinephrine reuptake inhibitor (NRI) program. Synthesis of a variety of heterocycles identified (+)-S-21, a potent NRI efficacious in an animal model for thermoregulatory dysfunction.

Substituted oxoazaheterocyclyl compounds

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Page/Page column 76-77, (2008/06/13)

This invention is directed to oxoazaheterocycyl compounds which inhibit Factor Xa, to oxoazaheterocycyl compounds which inhibit both Factor Xa and Factor IIa, to pharmaceutical compositions comprising these compounds, to intermediates useful for preparing these compounds, to a method of directly inhibiting Factor Xa and to a method of simultaneously directly inhibiting Factor Xa and Factor IIa..

Quinolones as gonadotropin releasing hormone (GnRH) antagonists: Simultaneous optimization of the C(3)-aryl and C(6)-substituents

Young, Jonathan R.,Huang, Song X.,Chen, Irene,Walsh, Thomas F.,DeVita, Robert J.,Wyvratt Jr., Matthew J.,Goulet, Mark T.,Ren, Ning,Lo, Jane,Yang, Yi Tien,Yudkovitz, Joel B.,Cheng, Kang,Smith, Roy G.

, p. 1723 - 1727 (2007/10/03)

A series of 3-arylquinolones was prepared and evaluated for their ability to act as gonadotropin releasing hormone (GnRH) antagonists. A variety of substitution patterns of the 3-aryl substituent are described. The 3,4,5-trimethylphenyl substituent (23h) was found to be optimal. (C) 2000 Elsevier Science Ltd. All rights reserved.

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