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81494-51-1

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81494-51-1 Usage

Molecular Structure

2-[(1-hydroxy-3-oxoprop-1-en-2-yl)carbamoyl]benzoic acid consists of a benzoic acid core and a hydroxy-oxo propenyl carbamoyl side chain.

Chemical Family

It is a member of the carboxylic acid family.

Common Uses

It is commonly used in pharmaceutical and industrial applications.

Biological Activity

It has the potential to exhibit strong biological activities due to its unique structural features.

Potential Applications

It is a promising candidate for drug development and other therapeutic purposes.

Further Research

More research is needed to fully understand its properties and potential uses.

Check Digit Verification of cas no

The CAS Registry Mumber 81494-51-1 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 8,1,4,9 and 4 respectively; the second part has 2 digits, 5 and 1 respectively.
Calculate Digit Verification of CAS Registry Number 81494-51:
(7*8)+(6*1)+(5*4)+(4*9)+(3*4)+(2*5)+(1*1)=141
141 % 10 = 1
So 81494-51-1 is a valid CAS Registry Number.

81494-51-1SDS

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 2-[[(E)-1-hydroxy-3-oxoprop-1-en-2-yl]carbamoyl]benzoic acid

1.2 Other means of identification

Product number -
Other names o-Carboxy-benzoylmalondialdehyd

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:81494-51-1 SDS

81494-51-1Upstream product

81494-51-1Downstream Products

81494-51-1Relevant articles and documents

Syntheses with Aliphatic Dialdehydes, XXXII. Syntheses and Reactions of N-Substituted 2-Aminomalondialdehydes

Reichardt, Christian,Rust, Ulrich

, p. 236 - 245 (2007/10/02)

The 2-aminomalondialdehyde bis 2 and some of its N-monosubstituted derivatives 7a-d as well as the o-carboxy benzoyl malondialdehyde 12 have been prepared.With heterocyclic imonium salts these amino malondialdehyde derivatives form, by a twofold condensation reaction, the γ-acylamino-substituted pentamethine cyanine dyes 15a-c, 17, and 18a-b, the UV/Vis and 13C NMR spectra of which are recorded with respect to the influence of the γ-substituent on these spectra. - Key words: 2-Aminomalondialdehyde Derivatives, γ-Acylaminopentamethinecyanine Dyes, UV/Vis Spectra, 13C NMR Spectra

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