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Propanoic acid, 3-[2-(acetylamino)-4-nitrophenoxy]- is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

89665-56-5

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89665-56-5 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 89665-56-5 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 8,9,6,6 and 5 respectively; the second part has 2 digits, 5 and 6 respectively.
Calculate Digit Verification of CAS Registry Number 89665-56:
(7*8)+(6*9)+(5*6)+(4*6)+(3*5)+(2*5)+(1*6)=195
195 % 10 = 5
So 89665-56-5 is a valid CAS Registry Number.

89665-56-5SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 17, 2017

Revision Date: Aug 17, 2017

1.Identification

1.1 GHS Product identifier

Product name 3-(2-acetamido-4-nitrophenoxy)propanoic 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:89665-56-5 SDS

89665-56-5Downstream Products

89665-56-5Relevant academic research and scientific papers

On the pharmaceutical and biopharmaceutical evaluation of acetylaminonitropropoxybenzene (falimint). Part IV. Biotransformation of the active agent

Gerlach,Buge,Peinhardt,Furst

, p. 42 - 45 (2007/10/02)

2-Acetamino-4-nitropropoxybenzene is metabolized almost completely. Till now in urine of man seven components have been detected. The main way of metabolism is the oxidation of propoxy group of a carboxyl group. Also the deacetylated compound of this acid has been found to a certain extent. A further metabolite is supposed to be oxidized in the side chain in another way. In a higher extent dealkylation to 2-acetamino-4-nitrophenol takes place which is eliminated probably in conjugation with glucuronic acid. Free 2-acetamino-4-nitrophenol and 2-amino-4-nitrophenol respectively are only detectable in traces. Deacetylation of 2-amino-4-nitropropoxybenzene takes place only in a very small extent. Till now metabolites with reduced nitro group haven't been found.

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