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4-ACETOXYMETHYLPHENYLACETIC ACID is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

61165-81-9

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61165-81-9 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 61165-81-9 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 6,1,1,6 and 5 respectively; the second part has 2 digits, 8 and 1 respectively.
Calculate Digit Verification of CAS Registry Number 61165-81:
(7*6)+(6*1)+(5*1)+(4*6)+(3*5)+(2*8)+(1*1)=109
109 % 10 = 9
So 61165-81-9 is a valid CAS Registry Number.

61165-81-9SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 20, 2017

Revision Date: Aug 20, 2017

1.Identification

1.1 GHS Product identifier

Product name 2-[4-(acetyloxymethyl)phenyl]acetic acid

1.2 Other means of identification

Product number -
Other names acetyl-OMPA

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:61165-81-9 SDS

61165-81-9Relevant articles and documents

COMPOSITIONS OF ALKYLAMIDOTHIAZOLES AND FRAGRANCES

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Paragraph 0076; 0077; 0078; 0079, (2016/02/12)

Disclosed are active ingredient combinations of alkylamidothiazoles and one or more cosmetically or dermatologically relevant fragrances.

COMPOSITIONS OF ALKYLAMIDOTHIAZOLES AND UV-FILTER SUBSTANCES

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Paragraph 0097-0100, (2016/02/28)

Disclosed are active ingredient combinations of alkylamidothiazoles and one or more cosmetically or dermatologically acceptable UV-filter substances.

COMBINATIONS OF ALKYLAMIDOTHIAZOLES AND PRESERVATIVES

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Page/Page column 0067; 0068; 0075; 0076, (2016/02/10)

Disclosed are active ingredient combinations of alkylamidothiazoles and one or more cosmetically or dermatologically acceptable preservatives.

ALKYLAMIDOTHIAZOLES, COSMETIC OR DERMATOLOGICAL PREPARATIONS CONTAINING SAID ALKYLAMIDOTHIAZOLES, AND USE THEREOF TO COMBAT OR PREVENT UNDESIRED PIGMENTATION OF THE SKIN

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Paragraph 0064; 0067, (2014/05/08)

Alkylamidothiazoles of general formula (I), wherein R 1=—C1-C24 alkyl (linear and branched), —C1-C24 alkenyl (linear and branched), —C1-C8 cycloalkyl, —C1-C8 cycloalkyl-alkylhydroxy, —C1-C24 alkylhydroxy (linear and branched), —C1-C24 alkylamine (linear and branched), —C1-C24 alkylaryl (linear and branched), —C1-C24 alkylaryl-alkyl-hydroxy (linear and branched), —C1-C24 alkyl-heteroaryl (linear and branched), —C1-C24-alkyl-O—C1-C24-alkyl (linear and branched), —C1-C24 alkyl morpholino, —C1-C24 alkyl piperidino, —C1-C24 alkyl piperazino, —C1-C24 alkyl-piperazino-N-alkyl, as well as cosmetic or dermatological preparations having an effective content of one or more alkylamidothiazoles, as well as the use thereof for the cosmetic or dermatological treatment and/or prophylaxis of undesired skin pigmentation.

Synthesis and anti-inflammatory activity of the major metabolites of imrecoxib

Feng, Zhiqiang,Chu, Fengming,Guo, Zongru,Sun, Piaoyang

body text, p. 2270 - 2272 (2009/12/03)

We have developed a novel and moderately selective COX-2 inhibitor, imrecoxib, as a new anti-inflammatory drug. We describe herein the preparation of the major metabolites M2 and M4 of imrecoxib, as well as the in vitro and in vivo activities of the two c

Electron-transfer Processes: Oxidation of Arylacetic Acids by Peroxydisulphate in Acetic Acid

Giordano, Claudio,Beili, Aldo,Citterio, Attilio,Minisci, Francesco

, p. 1574 - 1576 (2007/10/02)

The oxidation of arylacetic acids by peroxydisulphate in acetic acid media in the presence of potassium and copper(II) acetates leads to the corresponding benzylacetates.The mechanism of the reaction is rationalized by the occurrence of two pathways: the intermediate formation of aromatic radical cations or the direct decarboxylation of the arylacetate ion.The importance of acetic acid as reaction medium is stressed.

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