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6725-64-0

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6725-64-0 Usage

Chemical Properties

Colorless liquid; pungent odor.

Check Digit Verification of cas no

The CAS Registry Mumber 6725-64-0 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 6,7,2 and 5 respectively; the second part has 2 digits, 6 and 4 respectively.
Calculate Digit Verification of CAS Registry Number 6725-64:
(6*6)+(5*7)+(4*2)+(3*5)+(2*6)+(1*4)=110
110 % 10 = 0
So 6725-64-0 is a valid CAS Registry Number.
InChI:InChI=1/CH4S2/c2-1-3/h2-3H,1H2

6725-64-0SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 19, 2017

Revision Date: Aug 19, 2017

1.Identification

1.1 GHS Product identifier

Product name methanedithiol

1.2 Other means of identification

Product number -
Other names methylene dithiol

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:6725-64-0 SDS

6725-64-0Relevant articles and documents

NEUE ERGEBNISSE BEI DER SPALTUNG VON THIOETHERN MIT NATRIUM IN FLUESSIGEM AMMONIAK. ABTRENNUNG VON 1.3.5-TRITHIAPENTAN UEBER 1.5-BIS-(TRIMETHYLSILYL)-1.3.5-TRITHIAPENTAN ALS ZWISCHENSTUFE

Weissflog, Eckhard

, p. 233 - 240 (2007/10/02)

Recent results show that the cleavage of oligomeric and polymeric thioformaldehydes or polymethylenedisulfide by sodium in liquid ammonia, followed by treatment with an excess of hydrochloric acid, leads to the formation of mercaptothioethers, CH3(SCH2)nSH, bis-mercaptothioethers, HS(CH2S)mH and thioalkanes, CH3(SCH2)xSCH3.The identification and isolation of various components of these mixtures are described.The separation of pure 1.3.5-trithiapentane by silylation, distillation and cleavage with hydrogen chloride is of interest for its synthesis starting from easily available compounds like s-trithiane, polymethylenesulfide or polymethylenedisulfide.The silylated derivatives of 1.3.5-trithiahexane and 1.3.5-trithiapentane are described.

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