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420-32-6

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420-32-6 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 420-32-6 includes 6 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 3 digits, 4,2 and 0 respectively; the second part has 2 digits, 3 and 2 respectively.
Calculate Digit Verification of CAS Registry Number 420-32:
(5*4)+(4*2)+(3*0)+(2*3)+(1*2)=36
36 % 10 = 6
So 420-32-6 is a valid CAS Registry Number.
InChI:InChI=1/CF2S/c2-1(3)4

420-32-6SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 14, 2017

Revision Date: Aug 14, 2017

1.Identification

1.1 GHS Product identifier

Product name difluoromethanethione

1.2 Other means of identification

Product number -
Other names CSF2

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:420-32-6 SDS

420-32-6Relevant articles and documents

CO2 LASER-INDUCED INTERACTION BETWEEN SULFUR HEXAFLUORIDE AND CARBON DISULFIDE

Pola, J.,Horak, M.,Engst, P.

, p. 37 - 44 (1981)

Interaction between carbon disulfide and sulfur hexafluoride is excited by cw CO2 laser radiation and has been investigated for different ratiosover a pressure range from 3.1 to 34.6 kPa.The reaction yields sulfur tetrafluoride, sulfur, carbon, thiocarbonyl fluoride, tetrafluoromethane and hexafluoroethane, the ratio of these latter products is dependent on the partial pressure of sulfur hexafluoride in the initial CS2-SF6 mixture.Interaction is considered to include both the SF6-sensitized decomposition of carbon disulfide and reaction between sulfur hexafluoride and carbon disulfide.

Unusual reaction of Grignard reagents with bis(trifluoromethyl)disulfide

Munavalli, S.,Rossman, D. I.,Rohrbaugh, D. K.,Ferguson, C. P.

, p. 147 - 153 (2007/10/02)

Simultaneous scission of the C-S and S-S bonds of bis(trifluoromethyl)disulfide occurs on treatment with Grignard reagents at -78 deg C and gives rise to unsymmetrical disulfides and sulfides as well as alkyl sulfides.Under similar experimental conditions, alkyl disulfides are recovered unreacted.Probable mechanisms of the cleavage reactions are presented.

TRANSFORMATION OF ORGANOPHOSPHORUS S-TRIFLUOROMETHYLTHIOATES RR'P(O)SCF3 INTO FLUORIDES RR'P(O)F. STEREOCHEMICAL ASPECTS OF THIOCARBONYL FLUORIDE EXTRUSION

Lopusinski, Andrezej

, p. 383 - 390 (2007/10/02)

The stereochemical course of the thermal or by nucleophiles catalyzed extrusion reaction of thiocarbonyl fluoride from two diastereomeric (6) and optically active (10) organophosphorus S-trifluoromethylthioates has been investigated.To explain the observed retention of configuration at phosphorus in fluoridates 7 formed in the thermal reactions, a four center transition state for such reactions has been proposed.The lack of the stereoselectivity in the catalyzed reactions of 6, and the observed racemization of the final product 11 are briefly discussed.

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