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Acetic acid, [4-(2-hydroxyethyl)phenoxy]-, ethyl ester is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

140893-10-3

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140893-10-3 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 140893-10-3 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,4,0,8,9 and 3 respectively; the second part has 2 digits, 1 and 0 respectively.
Calculate Digit Verification of CAS Registry Number 140893-10:
(8*1)+(7*4)+(6*0)+(5*8)+(4*9)+(3*3)+(2*1)+(1*0)=123
123 % 10 = 3
So 140893-10-3 is a valid CAS Registry Number.

140893-10-3SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 14, 2017

Revision Date: Aug 14, 2017

1.Identification

1.1 GHS Product identifier

Product name ethyl 2-[4-(2-hydroxyethyl)phenoxy]acetate

1.2 Other means of identification

Product number -
Other names Acetic acid,[4-(2-hydroxyethyl)phenoxy]-,ethyl 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:140893-10-3 SDS

140893-10-3Relevant academic research and scientific papers

Crystal polymorphism of aminoethylphenoxyacetic acid derivative

-

, (2008/06/13)

The present invention relates to a crystalline polymorph of 2-[4-[2-[[(1S,2R)-2-hydroxy-2-(4-hydroxy-phenyl)-1-methylethyl]amino]ethyl]phenoxy]acetic acid having strong diffraction peaks (diffraction angle: 2θ±0.1°) at 10.8, 19.1, 19.3, 19.8, 20.6 and 27.

Synthesis and evaluation of novel thiazolidine derivatives as thromboxane A2 receptor antagonists

Sato,Kawashima,Goto,Yamane,Chiba,Jinno,Satake,Imanishi,Iwata

, p. 521 - 529 (2007/10/02)

A series of 3-benzoyl or 3-phenylsulfonyl-2-substituted thiazolidine derivatives were synthesized, and evaluated for their thromboxane A2 (TXA2) receptor-antagonizing effect on (15S)-15-hydroxy-11α,9α- (epoxymethano)prosta-5(Z),13(E)-dienoic acid (U-46619)-induced aggregation of rabbit platelet-rich plasma (PRP). A simple 2-arylthiazolidine derivative, 3- benzoyl-2-(4-hydroxy-3-methoxyphenyl)thiazolidine (5a), showed mild TXA2 receptor antagonist activity. Modification of 5a led to 2-chloro-4-[3-(4- chlorophenylsulfonyl)thiazolidin-2-ylmethyl]phenoxyaretic acid (29d), which showed 10 times more potent TXA2 receptor antagonist activity than 5a.

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