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3575-07-3

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3575-07-3 Usage

General Description

2,2'-ethane-1,2-diylbis-1H-benzimidazole, also known as EDBI, is a chemical compound that belongs to the class of benzimidazoles. It is commonly used as a fluorescent probe for the detection of metal ions, especially zinc ions, due to its high selectivity and sensitivity. EDBI has also been studied for its potential applications in biological and medical fields, including as a drug delivery agent and in imaging techniques for cancer detection. Additionally, it has been investigated for its antimicrobial and antiviral properties. Overall, EDBI is a versatile compound with diverse potential applications in research and industry.

Check Digit Verification of cas no

The CAS Registry Mumber 3575-07-3 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 3,5,7 and 5 respectively; the second part has 2 digits, 0 and 7 respectively.
Calculate Digit Verification of CAS Registry Number 3575-07:
(6*3)+(5*5)+(4*7)+(3*5)+(2*0)+(1*7)=93
93 % 10 = 3
So 3575-07-3 is a valid CAS Registry Number.

3575-07-3SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 13, 2017

Revision Date: Aug 13, 2017

1.Identification

1.1 GHS Product identifier

Product name 2-[2-(1H-benzimidazol-2-yl)ethyl]-1H-benzimidazole

1.2 Other means of identification

Product number -
Other names -

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:3575-07-3 SDS

3575-07-3Relevant articles and documents

Boric acid-catalyzed direct condensation of carboxylic acids with benzene-1,2-diamine into benzimidazoles

Maras, Nenad,Kocevar, Marijan

experimental part, p. 1860 - 1874 (2011/12/02)

The applicability of boric acid catalysis for the direct condensation of carboxylic acids with benzene-1,2-diamine to give 2-substituted benzimidazoles was investigated. It was found that catalytic amounts (5-10 mol-%) of boric acid efficiently promote the cyclocondensation of aliphatic carboxylic acids in refluxing toluene. In addition, the relatively neutral conditions allow the use of acid-sensitive substrates and give rise to specific transformations and selectivities that are not observed with some classical methods. Benzoic acids were found to be less reactive than aliphatic acids and thus require refluxing xylene for better efficiency. Phenylboronic acid was found to be inactive as a catalyst due to its rapid consumption by condensation with benzene-1,2-diamine to give a 2-phenylbenzodiazaborole. Copyright

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