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63399-98-4

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63399-98-4 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 63399-98-4 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 6,3,3,9 and 9 respectively; the second part has 2 digits, 9 and 8 respectively.
Calculate Digit Verification of CAS Registry Number 63399-98:
(7*6)+(6*3)+(5*3)+(4*9)+(3*9)+(2*9)+(1*8)=164
164 % 10 = 4
So 63399-98-4 is a valid CAS Registry Number.

63399-98-4SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 15, 2017

Revision Date: Aug 15, 2017

1.Identification

1.1 GHS Product identifier

Product name 4-[(6-oxocyclohexa-2,4-dien-1-ylidene)methylamino]butanoic acid

1.2 Other means of identification

Product number -
Other names N-salicylidene-4-aminobutyric acid

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:63399-98-4 SDS

63399-98-4Relevant articles and documents

Functionalities of conjugated compounds of γ-aminobutyric acid with salicylaldehyde or cinnamaldehyde

Liu, Tai-Ti,Tseng, Yi-Wei,Yang, Tsung-Shi

, p. 1102 - 1108 (2015)

Aldehydes or ketones can react with amino compounds to form Schiff base adducts, which have been widely studied and shown to exhibit antimicrobial, antioxidant or antiviral activity. Salicylaldehyde (SA) and cinnamaldehyde (CA) are components of plant ess

New Biologically Active Aromatic Derivatives of Fatty Acids

Lurie, E. Yu.,Kaplun, A. P.,Kulakov, V. N.,Shvets, V. I.

, p. 264 - 268 (2007/10/02)

A convenient method for synthesizing the homologous series of new aromatic derivatives of fatty acids is described.The synthetic approach includes the reductive alkylation of ω- and α-amino acids with hydroxybenzaldehydes.The physicochemical properties of

Transition-state analogues as inhibitors for GABA-aminotransferase

Iskander, MN,Andrews, PR,Winkler, DA,Brinkworth, RI,Paola, C Di,et al.

, p. 129 - 136 (2007/10/02)

Our previous calculations on the reaction catalysed by GABA-aminotransferase (GABA-T) have been utilized in this work in order to synthesize a series of reversible inhibitors of this enzyme.The synthesized transition-state analogues and their precursors i

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