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Sorbohydroxamic acid, a synthetic organic compound with the chemical formula C5H10N3O3, is derived from hydroxamic acid. It is known for its strong complexation properties, enabling it to form stable complexes with various metal ions such as copper, iron, and uranium. This unique characteristic positions sorbohydroxamic acid as a versatile chelating agent in industrial applications, including metal separation and extraction processes. Furthermore, its potential medicinal properties, particularly in the treatment of various forms of cancer, make it a subject of interest for pharmaceutical research and development.

4076-62-4

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4076-62-4 Usage

Uses

Used in Industrial Applications:
Sorbohydroxamic acid is used as a chelating agent for metal separation and extraction processes due to its strong complexation properties with a variety of metal ions, enhancing the efficiency of these processes.
Used in Pharmaceutical Research:
Sorbohydroxamic acid is being studied as a potential treatment for various forms of cancer. Its ability to bind to metal ions and inhibit certain enzymatic processes makes it a promising candidate for further research and development in the pharmaceutical industry. This application is based on its potential to target and disrupt metal-dependent biological pathways in cancer cells, thereby exhibiting anticancer activity.

Check Digit Verification of cas no

The CAS Registry Mumber 4076-62-4 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 4,0,7 and 6 respectively; the second part has 2 digits, 6 and 2 respectively.
Calculate Digit Verification of CAS Registry Number 4076-62:
(6*4)+(5*0)+(4*7)+(3*6)+(2*6)+(1*2)=84
84 % 10 = 4
So 4076-62-4 is a valid CAS Registry Number.
InChI:InChI=1/C6H9NO2/c1-2-3-4-5-6(8)7-9/h2-5,9H,1H3,(H,7,8)/b3-2+,5-4+

4076-62-4SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 11, 2017

Revision Date: Aug 11, 2017

1.Identification

1.1 GHS Product identifier

Product name SORBOHYDROXAMIC ACID

1.2 Other means of identification

Product number -
Other names n-hydroxy-4-hexadienamide

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:4076-62-4 SDS

4076-62-4Upstream product

4076-62-4Downstream Products

4076-62-4Relevant academic research and scientific papers

Synthesis of hydroxamic acids by activation of carboxylic acids with N,N'-carbonyldiimidazole: Exploring the efficiency of the method

Usachova, Natalija,Leitis, Gundars,Jirgensons, Aigars,Kalvinsh, Ivars

experimental part, p. 927 - 935 (2010/05/01)

Activation of carboxylic acids with N,N'-carbonyldiimidazole followed by the reaction with anhydrous or aqueous hydroxylamine hydrochloride was demonstrated to be an operationally simple method for the synthesis of hydroxamic acids in good yield and high purity after aqueous workup. The potential by-product, N,O-diacylhydroxylamine, is cleanly transformed to hydroxamic acid in these reaction conditions.

An expeditious hydroxyamidation of carboxylic acids

Ech-Chahad, Abdellah,Minassi, Alberto,Berton, Luca,Appendino, Giovanni

, p. 5113 - 5115 (2007/10/03)

Capitalizing on in situ activation with the cyclic phosphonic anhydride PPAA (1), the conversion of carboxylic acids into hydroxamic acids has been reduced to an experimentally simple one-pot operation that addresses the issue of polyacylation without resorting to a large excess of hydroxylamine or to protection. Scope and selectivity were satisfactory with a wide range of substrates, including α,β-unsaturated acids and hydroxyacids.

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