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136099-55-3

N-(2,6-DICHLORO-4-METHOXYPHENYL)ACETAMIDE is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

136099-55-3

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136099-55-3 Usage

Chemical Properties

White Solid

Check Digit Verification of cas no

The CAS Registry Mumber 136099-55-3 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,3,6,0,9 and 9 respectively; the second part has 2 digits, 5 and 5 respectively.
Calculate Digit Verification of CAS Registry Number 136099-55:
(8*1)+(7*3)+(6*6)+(5*0)+(4*9)+(3*9)+(2*5)+(1*5)=143
143 % 10 = 3
So 136099-55-3 is a valid CAS Registry Number.
InChI:InChI=1/C9H9Cl2NO2/c1-5(13)12-9-7(10)3-6(14-2)4-8(9)11/h3-4H,1-2H3,(H,12,13)

136099-55-3SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 18, 2017

Revision Date: Aug 18, 2017

1.Identification

1.1 GHS Product identifier

Product name N-(2,6-Dichloro-4-methoxyphenyl)acetamide

1.2 Other means of identification

Product number -
Other names HMS563C02

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:136099-55-3 SDS

136099-55-3Relevant articles and documents

Synthesis of deuterium labelled 4'-hydroxydiclofenac

Waterhouse, Ian

, p. 1075 - 1083 (2007/10/03)

Diclofenac is a potentially useful substrate for the study of drug-drug interactions caused by modulation of the activity of specific isoforms of cytochrome P450. The synthesis of a deuterium labelled version of its principal human metabolite, 4'-hydroxydiclofenac, for use as an internal standard in LC-MS-MS studies, is described.

Hepatic metabolism of diclofenac: Role of human CYP in the minor oxidative pathways

Bort, Roque,MacE, Katherine,Boobis, Alan,Gomez-Lechon, Maria-Jose.,Pfeifer, Andrea,Castell, Jose

, p. 787 - 796 (2007/10/03)

The aim of this study was to re-examine the human hepatic metabolism of diclofenac, with special focus on the generation of minor hydroxylated metabolites implicated in the idiosyncratic hepatotoxicity of the drug. Different experimental approaches were u

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