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151675-59-1

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151675-59-1 Usage

Uses

5-?(Dimethylamino)?-?5-?oxopentanoic Acid acts as a reagent in the synthesis of leukotriene B4 analogs for improved receptor binding activity.

Check Digit Verification of cas no

The CAS Registry Mumber 151675-59-1 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,5,1,6,7 and 5 respectively; the second part has 2 digits, 5 and 9 respectively.
Calculate Digit Verification of CAS Registry Number 151675-59:
(8*1)+(7*5)+(6*1)+(5*6)+(4*7)+(3*5)+(2*5)+(1*9)=141
141 % 10 = 1
So 151675-59-1 is a valid CAS Registry Number.

151675-59-1SDS

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 5-(Dimethylamino)-5-oxopentanoic acid

1.2 Other means of identification

Product number -
Other names Pentanoic acid,5-(dimethylamino)-5-oxo

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:151675-59-1 SDS

151675-59-1Relevant articles and documents

Enolic Radical Derived from Acetic Acid: A Useful Radical Alternative to Acetate Enolate in Michael-Type Reactions

Foubelo, Francisco,Lloret, Francisco,Yus, Miguel

, p. 8465 - 8470 (1993)

The reaction of iodoacetic acid 1 with tributyltin chloride and sodium borohydride in the presence of different electrophilic olefins 2 (methyl, allyl or tert-butyl acrylates, N,N-dimethyl or N,N-di-iso-propyl acrylamides, acrylonitrile, methyl methacrylate, methacrylonitrile and 1,1-dichloroethylene) and AIBN as an initiator yields, after treatment with aqueous sodium fluoride, the corresponding products 3 through a radical Michael-type process.

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