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344567-18-6

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344567-18-6 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 344567-18-6 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 3,4,4,5,6 and 7 respectively; the second part has 2 digits, 1 and 8 respectively.
Calculate Digit Verification of CAS Registry Number 344567-18:
(8*3)+(7*4)+(6*4)+(5*5)+(4*6)+(3*7)+(2*1)+(1*8)=156
156 % 10 = 6
So 344567-18-6 is a valid CAS Registry Number.

344567-18-6SDS

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 3-hydroxy-4-[[(2-hydroxy-4-oxocyclohexa-2,5-dien-1-ylidene)-sulfanylmethyl]sulfinyl-sulfanylmethylidene]cyclohexa-2,5-dien-1-one

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:344567-18-6 SDS

344567-18-6Downstream Products

344567-18-6Relevant articles and documents

Interplay of Inter- and Intramolecular Interactions in Crystal Structures of 1,3,4-Thiadiazole Resorcinol Derivatives

Hoser, Anna A.,Kamiński, Daniel M.,Skrzypek, Alicja,Matwijczuk, Arkadiusz,Niewiadomy, Andrzej,Gago?, Mariusz,Wo?niak, Krzysztof

, p. 3851 - 3862 (2018/06/11)

Five new 1,3,4-thiadiazole derivatives have been synthesized, and their crystal structures have been determined by single crystal X-ray diffraction. The influence of substituents on molecular geometry and the three-dimensional arrangement of molecules has

A new approach to the synthesis of 2-aryl-substituted benzimidazoles, quinazolines, and other related compounds and their antibacterial activity

Los, Renata,Wesolowska-Trojanowska, Marta,Malm, Anna,Karpiaska, Monika M.,Matysiak, Joanna,Niewiadomy, Andrzej,Glaszcz, Urszula

body text, p. 265 - 275 (2012/09/08)

A new synthesis method of benzimidazoles, dihydroquinazolines, and other related compounds containing a 2,4-dihydroxyphenyl moiety was elaborated. Their structures were identified from elemental, infrared, 1H NMR, 13C NMR, and mass spectra analyses. The minimal inhibitory concentration values of the compounds toward eight reference bacterial strains were determined by the two-fold serial microdilution broth method. The compounds exhibited substantial inhibitory effects against the Gram-positive strains tested contrary to Gram-negative ones. The compounds of imidazopyridine, N-methylbenzimidazole, and dihydroquinazoline structures exhibited the largest activity. The magnification of covering a two-nitrogen atom heterocyclic ring fused to a benzene one decreases the biological effect.

Application of sulfinyl bis(2,4-dihydroxythiobenzoyl) in the synthesis of N-substituted 2-amino-5-(2,4-dihydroxyphenyl)-1,3,4-thiadiazoles

Matysiak, Joanna,Niewiadomy, Andrzej

, p. 1621 - 1630 (2007/10/03)

One-stage synthesis of N-substituted 2-amino-5-(2,4-dihydroxyphenyl)-1,3,4-thiadiazoles is described. The compounds were prepared by the reaction of the sulfinyl bis(2,4-dihydroxythiobenzoyl) (STB) with 4-substituted 3-thiosemicarbazides. STB was obtained

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