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3-Pyridinepropanamide, b-oxo- is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

152171-44-3

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152171-44-3 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 152171-44-3 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,5,2,1,7 and 1 respectively; the second part has 2 digits, 4 and 4 respectively.
Calculate Digit Verification of CAS Registry Number 152171-44:
(8*1)+(7*5)+(6*2)+(5*1)+(4*7)+(3*1)+(2*4)+(1*4)=103
103 % 10 = 3
So 152171-44-3 is a valid CAS Registry Number.

152171-44-3SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 19, 2017

Revision Date: Aug 19, 2017

1.Identification

1.1 GHS Product identifier

Product name 3-oxo-3-(3-pyridyl)propanamide

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:152171-44-3 SDS

152171-44-3Upstream product

152171-44-3Downstream Products

152171-44-3Relevant academic research and scientific papers

Preparation of N-unsubstituted β-ketoamides by Rhodococcus rhodochrous-catalysed hydration of β-ketonitriles

Gotor, Vicente,Liz, Ramón,Testera, Ana Ma

, p. 607 - 618 (2004)

A varied set of N-unsubstituted β-ketoamides, hardly obtainable or non-accessible by non-enzymatic methods, have been synthesized, with good to excellent yields, by the generally fast hydration of the corresponding β-ketonitriles, catalysed by the bacterium Rhodococcus rhodochrous IFO 15564. This bacterium shows nitrile hydratase and amidase activities, the latter being inhibited during its growth phase with diethyl phosphoramidate (DEPA). Optimization of the processes and studies concerning large-scale biotransformations were also carried out. β-Ketoamides exist as keto-enol mixtures whose composition depends on their substituents and varies with solvent polarity.

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