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49561-47-9

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49561-47-9 Usage

Structure

A thiazole ring fused to a furan ring with a nitro group attached to the furan ring and a vinyl group attached to the thiazole ring

+ Antimicrobial

The compound has been studied for its ability to inhibit the growth of microorganisms

+ Antitumor

The compound has been studied for its potential to prevent the growth of cancer cells

+ Biological activity

The nitrofuran and thiazole moieties in the compound are known to possess biological activities, making it a potentially significant molecule in medicinal chemistry research.

Check Digit Verification of cas no

The CAS Registry Mumber 49561-47-9 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 4,9,5,6 and 1 respectively; the second part has 2 digits, 4 and 7 respectively.
Calculate Digit Verification of CAS Registry Number 49561-47:
(7*4)+(6*9)+(5*5)+(4*6)+(3*1)+(2*4)+(1*7)=149
149 % 10 = 9
So 49561-47-9 is a valid CAS Registry Number.

49561-47-9SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 17, 2017

Revision Date: Aug 17, 2017

1.Identification

1.1 GHS Product identifier

Product name 2-[2-(5-nitrofuran-2-yl)ethenyl]-1,3-thiazole

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:49561-47-9 SDS

49561-47-9Downstream Products

49561-47-9Relevant articles and documents

Chemotherapeutic nitroheterocycles. Antischistosomal properties of nitrofurylvinyl and nitrothienylvinyl heterocycles

Henry,Brown,Cory,et al.

, p. 1287 - 1291 (2007/10/05)

A series of 24 analogs of the experimental antischistosomal agent, 5 amino 3 [2 (5 nitro 2 furyl) vinyl] 1,2,4 oxadiazole, was prepared and evaluated in mice infected with Schistosoma mansoni. Although antischistosomal activity was widespread in the series, only four of the compounds showed significant curative properties. Compounds containing 2 imidazolyl and 2 pyridyl groups gave cure rates around 25% at 400 and 250 mg/kg dose levels, respectively. The 2 thiazolyl and 2 pyrimidyl derivatives were especially notable, yielding 100% cures at 250 and 200 mg/kg dose levels, respectively.

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