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8-BROMO-6-CHLORO-2H-CHROMENE-3-CARBONITRILE is a chemical compound that belongs to the family of chromene derivatives. It is characterized by its unique structure, which includes a chromene ring with bromine and chlorine substitutions, as well as a carbonitrile group attached to the third position of the ring.

885271-10-3

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885271-10-3 Usage

Uses

Used in Pharmaceutical Applications:
8-BROMO-6-CHLORO-2H-CHROMENE-3-CARBONITRILE is used as a scaffold for drug design due to its potential biological activities, including antimicrobial, antifungal, and anti-inflammatory properties.
Used in Organic and Medicinal Chemistry Research:
8-BROMO-6-CHLORO-2H-CHROMENE-3-CARBONITRILE is used as an interesting target for further research and development in the field of organic and medicinal chemistry, due to its chemical reactivity and structural features.

Check Digit Verification of cas no

The CAS Registry Mumber 885271-10-3 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 8,8,5,2,7 and 1 respectively; the second part has 2 digits, 1 and 0 respectively.
Calculate Digit Verification of CAS Registry Number 885271-10:
(8*8)+(7*8)+(6*5)+(5*2)+(4*7)+(3*1)+(2*1)+(1*0)=193
193 % 10 = 3
So 885271-10-3 is a valid CAS Registry Number.

885271-10-3SDS

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 8-BROMO-6-CHLORO-2H-CHROMENE-3-CARBONITRILE

1.2 Other means of identification

Product number -
Other names 2H-1-Benzopyran-3-carbonitrile,8-bromo-6-chloro

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:885271-10-3 SDS

885271-10-3Downstream Products

885271-10-3Relevant academic research and scientific papers

Microwave-Assisted Rapid and Efficient Synthesis of New Series of Chromene-Based 1,2,4-Oxadiazole Derivatives and Evaluation of Antibacterial Activity with Molecular Docking Investigation

Baral, Nilofar,Mohapatra, Seetaram,Raiguru, Bishnu Prasad,Mishra, Nilima Priyadarsini,Panda, Pravati,Nayak, Sabita,Pandey, Satyendra Kumar,Kumar, P. Sudhir,Sahoo, Chita Ranjan

, p. 552 - 565 (2019)

A new series of novel chromene-based oxadiazole derivatives were synthesized from a variety of chromene-based amidoximes with readily available carboxylic acids under conventional oil bath heating as well as under microwave irradiation. The use of commercially available EDCI and HOBt as coupling reagents in DMF combined with microwave heating resulted in high yields and purities of the product 1,2,4-oxadiazoles in an expeditious manner. This methodology is successfully applied to synthesize 18 numbers of new 2H-chromene-substituted 1,2,4-oxadiazole derivatives in good to high yields. The structure of the product was ascertained by X-ray crystallographic analysis. All the synthesized compounds were evaluated for their in vitro antibacterial activity against two different pathogenic bacterial strains, that is, Escherichia coli (MTCC614) and Klebsiella pneumoniae (MTCC4031). The obtained results from in vitro antimicrobial assays indicated that 6g and 6h exhibited good antibacterial activity nearer to the standard drug, gentamicin. The molecular docking studies showed that compounds 6g and 6h show hydrogen bonding interaction with the bacterial target DNA gyrase of E.?coli.

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