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67002-21-5

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67002-21-5 Usage

Structure

A trisoxime derivative of trimesic acid

Appearance

Yellow crystalline solid

Solubility

Soluble in water, slightly soluble in organic solvents

Application

Chelating agent in metal ion coordination complexes

Affinity

High affinity for various metal ions

Use

Selective extraction and separation of metal ions in aqueous solutions

Potential applications

Environmental remediation, removal of toxic heavy metals from contaminated water sources

Other uses

Pharmaceutical industry, building block for the synthesis of novel organic compounds

Coordination chemistry

Widely studied for its potential applications in coordination chemistry

Organic synthesis

Used in organic synthesis for the preparation of various organic compounds

Environmental significance

Important for the treatment of contaminated water sources

Research focus

Investigated for its potential use in pharmaceuticals and novel organic compound synthesis

Check Digit Verification of cas no

The CAS Registry Mumber 67002-21-5 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 6,7,0,0 and 2 respectively; the second part has 2 digits, 2 and 1 respectively.
Calculate Digit Verification of CAS Registry Number 67002-21:
(7*6)+(6*7)+(5*0)+(4*0)+(3*2)+(2*2)+(1*1)=95
95 % 10 = 5
So 67002-21-5 is a valid CAS Registry Number.

67002-21-5SDS

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 N-[[3,5-bis(hydroxyiminomethyl)phenyl]methylidene]hydroxylamine

1.2 Other means of identification

Product number -
Other names 1,3,5-Benzenetricarboxaldehyde,trioxime

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:67002-21-5 SDS

67002-21-5Upstream product

67002-21-5Downstream Products

67002-21-5Relevant articles and documents

A versatile and green mechanochemical route for aldehyde-oxime conversions

Aakeroey, Christer B.,Sinha, Abhijeet S.,Epa, Kanishka N.,Spartz, Christine L.,Desper, John

supporting information, p. 11289 - 11291,3 (2012/12/12)

A robust, facile and solvent-free mechanochemical path for aldehyde-oxime transformations using hydroxylamine and NaOH is explored; the method is suitable for aromatic and aliphatic aldehydes decorated with a range of substituents. This journal is

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