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21813-61-6

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21813-61-6 Usage

Molecular weight

263.29 g/mol

Physical state

White solid

Structural features

Morpholine ring, phenyl group attached to a butanoic acid backbone

Usage

Organic synthesis, pharmaceutical research, potential applications in drug development

Potential properties

Biological activity, could be used as a starting material for the synthesis of derivatives with pharmacological properties

Further research needed

To fully understand its potential uses and effects.

Check Digit Verification of cas no

The CAS Registry Mumber 21813-61-6 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 2,1,8,1 and 3 respectively; the second part has 2 digits, 6 and 1 respectively.
Calculate Digit Verification of CAS Registry Number 21813-61:
(7*2)+(6*1)+(5*8)+(4*1)+(3*3)+(2*6)+(1*1)=86
86 % 10 = 6
So 21813-61-6 is a valid CAS Registry Number.

21813-61-6SDS

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 2-morpholin-4-yl-4-oxo-4-phenylbutanoic acid

1.2 Other means of identification

Product number -
Other names 2-Morpholino-4-oxo-4-phenyl-buttersaeure

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:21813-61-6 SDS

21813-61-6Relevant articles and documents

Lactones, XVIII: Synthesis of Lactone-Bridged 1,1-Diarylpropanamines

Lehmann, Jochen,Gossen, Axel

, p. 443 - 445 (2007/10/02)

Synthesis of the 3-amino-5,5-diaryl-4,5-dihydro-2(3H)-furanones 6a-h by addition of amines to the β-aroylacrylic acids 1-4 and treatment of 5a-h with phenyllithium closes the gap in the homologous series of γ-lactonized diarylalkanamines.

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