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88674-82-2

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88674-82-2 Usage

General Description

ART-CHEM-BB B015833 is a chemical compound used as a research reagent in various scientific applications. It is a white solid with a molecular formula of C7H7Cl2NO2 and a molecular weight of 208.04 g/mol. ART-CHEM-BB B015833 is often used in the synthesis and development of pharmaceuticals, as well as in biochemical and chemical research. It is important to handle this compound with care and follow proper safety protocols, as it may pose health risks if not used properly. ART-CHEM-BB B015833 is widely available for purchase from chemical suppliers and is an essential tool for scientists and researchers in the field.

Check Digit Verification of cas no

The CAS Registry Mumber 88674-82-2 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 8,8,6,7 and 4 respectively; the second part has 2 digits, 8 and 2 respectively.
Calculate Digit Verification of CAS Registry Number 88674-82:
(7*8)+(6*8)+(5*6)+(4*7)+(3*4)+(2*8)+(1*2)=192
192 % 10 = 2
So 88674-82-2 is a valid CAS Registry Number.
InChI:InChI=1/C9H7NO2S2/c1-5-2-3-6(12-5)4-7-8(11)10-9(13)14-7/h2-4H,1H3,(H,10,11,13)/b7-4+

88674-82-2SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 15, 2017

Revision Date: Aug 15, 2017

1.Identification

1.1 GHS Product identifier

Product name 5-[(5-methylfuran-2-yl)methylidene]-2-sulfanylidene-1,3-thiazolidin-4-one

1.2 Other means of identification

Product number -
Other names 5-methylfurfuralrhodanine

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:88674-82-2 SDS

88674-82-2Relevant articles and documents

Synthesis and antimicrobial activity of some new N-glycosides of 2-thioxo-4-thiazolidinone derivatives

Metwally, Nadia Hanafy,Abdalla, Magda Ahmed,Mosselhi, Mosselhi Abdel Nabi,El-Desoky, Ebrahim Adel

scheme or table, p. 1135 - 1141 (2010/09/12)

5-Arylidene-2-thioxo-4-thiazolidinones 3a-f react with each of 2,3,4,6-tetra-O-acetyl-α-d-glucopyranosyl and α-d-galactopyranosyl bromides 4a,b in acetone in the presence of aqueous potassium hydroxide at room temperature to afford N-(2,3,4,6-tetra-O-acet

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