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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.

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.

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

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