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3354-42-5

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3354-42-5 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 3354-42-5 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 3,3,5 and 4 respectively; the second part has 2 digits, 4 and 2 respectively.
Calculate Digit Verification of CAS Registry Number 3354-42:
(6*3)+(5*3)+(4*5)+(3*4)+(2*4)+(1*2)=75
75 % 10 = 5
So 3354-42-5 is a valid CAS Registry Number.
InChI:InChI=1/C7H4S3/c8-7-5-3-1-2-4-6(5)9-10-7/h1-4H

3354-42-5SDS

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 1,2-benzodithiole-3-thione

1.2 Other means of identification

Product number -
Other names 3H-1,2-benzodithiol-3-thione

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:3354-42-5 SDS

3354-42-5Relevant articles and documents

Sulfur/DABCO Promoted Reductive Coupling/Annulation Cascade Reaction between o -Hydroxy/Amino Nitrobenzenes and Benzaldehydes

Dang, Minh-Huy Dinh,Nguyen, Linh Ho Thuy,Tran, Phuong Hoang

supporting information, p. 1687 - 1694 (2020/05/25)

Sulfur/DABCO was found to be an efficient reagent in promoting- the reductive coupling/annulation of o -nitrophenols or o -nitroanilines with benzaldehydes. This method represents a simple, straightforward, and green approach to the construction of benz-oxazoles and benzimidazoles.

STUDIES ON ORGANOPHOSPHORUS COMPOUNDS-XXXVI SIMPLE NEW ROUTES TO PHOSPHORINS FROM 2-HYDROXY-, 2-MERCAPTO-, AND 2-AMINOBENZOIC ACIDS AND THEIR DERIVATIVES

El-Barbary, A. A.,Lawesson, S.-O.

, p. 2641 - 2646 (2007/10/02)

2-Hydroxybenzoic acid heated with 2,4-bis(4-methoxyphenyl)-1,3,2,4-dithiadiphosphetane-2,4-disulfide, 1, gave 2-(p-methoxyphenyl)-4H-1,3,2-benzoxathiaphosphorin-4-one 2-sulfide, 3, and its thio analogue, 4, while its ethyl or phenyl esters gave 4 as the sole product. 2-Mercaptobenzoic acid and its ethyl ester when heated with 1 produced 3H-1,2-benzodithiole-3-one, 8, 3H-1,2-benzidithiole-3-thione, 9, and 2-(p-methoxyphenyl)-4H-1,3,2-benzodithia-phosphorin-4-one 2-sulfide, 10.The reaction of 2-aminobenzoic acid with 1 gave 1,2-dihydro-2-(p-methoxyphenyl)-4H-3,1,2-benzoxaphosphorin-4-one 2-sulfide, 12.Reactions of 1 with methyl 2-aminobenzoate and 2-aminobenzamides are described.Mechanistic considerations for the formation of the heterocyclic phosphorus compounds are presented.

STUDIES ON ORGANOPHOSPHORUS COMPOUNDS. THIATION OF 3,1-BENZOXATHIAN-4-ONES. NEW ROUTES TO 1,2-BENZISOTHIAZOLE-3(2H)-THIONES AND 3H-1,2-BENZODITHIOL-3-IMINES

El-Barbary, A. A.,Clausen, K.,Lawesson, S.-O.

, p. 3309 - 3316 (2007/10/02)

3,1-Benzoxathian-4-ones, 2, when heated with 2,4-bis(4-methoxyphenyl)-1,3,2,4-dithiadiphosphetane-2,4-disulfide, 1, or with P4S10 give one or more of the following products: 3,1-benzoxathian-4-thione, 3, 1,3-benzodithian-4-one, 4, 1,3-benzodithian-4-thion

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