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108912-14-7

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108912-14-7 Usage

Class

Propionic acid derivative

Use

Building block in pharmaceuticals and agrochemicals

Molecular weight

242.33 g/mol

Physical state

White to off-white solid

Solubility

Sparingly soluble in water, soluble in most organic solvents

Potential applications

Pharmaceuticals industry due to unique chemical structure and biological activity

Check Digit Verification of cas no

The CAS Registry Mumber 108912-14-7 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,0,8,9,1 and 2 respectively; the second part has 2 digits, 1 and 4 respectively.
Calculate Digit Verification of CAS Registry Number 108912-14:
(8*1)+(7*0)+(6*8)+(5*9)+(4*1)+(3*2)+(2*1)+(1*4)=117
117 % 10 = 7
So 108912-14-7 is a valid CAS Registry Number.

108912-14-7SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 13, 2017

Revision Date: Aug 13, 2017

1.Identification

1.1 GHS Product identifier

Product name 2-(4-Thiophen-3-yl-phenyl)-propionic acid

1.2 Other means of identification

Product number -
Other names -

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:108912-14-7 SDS

108912-14-7Downstream Products

108912-14-7Relevant articles and documents

Synthesis and evaluation of S-4-(3-thienyl)phenyl-α-methylacetic acid

Mittal, Shilpi,Malde, Alpeshkumar,Selvam,Arun,Johar,Jachak, Sanjay M.,Ramarao,Bharatam,Chawla

, p. 979 - 982 (2007/10/03)

Herein we report an efficient procedure to synthesize S-4-(3-thienyl) phenyl-α-methylacetic acid, an enantiomerically pure intermediate of a recently approved nonsteroidal antiinflammatory cyclooxygenase inhibitor, atliprofen [methyl RS-4-(3-thienyl)phenyl-α-methylacetate]. The interactions of the active S-isomer of the acid were theoretically compared with those of S-ibuprofen through molecular docking studies using COX-1 and COX-2 protein structures. The results were corroborated by in vitro and in vivo studies.

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