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Phosphonothioic difluoride, methyl-, also known as methylphosphonothioic difluoride or methyldifluorophosphine sulfide, is a chemical compound with the formula (CH3)P(F)S. It is a colorless, volatile liquid that is highly reactive and sensitive to moisture and air. Phosphonothioic difluoride, methyl- is primarily used as a reagent in the synthesis of various organophosphorus compounds, particularly in the preparation of pesticides and pharmaceuticals. Due to its high reactivity, it is essential to handle this chemical with extreme caution, using appropriate safety measures and equipment to prevent exposure and potential hazards.

753-72-0

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753-72-0 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 753-72-0 includes 6 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 3 digits, 7,5 and 3 respectively; the second part has 2 digits, 7 and 2 respectively.
Calculate Digit Verification of CAS Registry Number 753-72:
(5*7)+(4*5)+(3*3)+(2*7)+(1*2)=80
80 % 10 = 0
So 753-72-0 is a valid CAS Registry Number.

753-72-0SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 18, 2017

Revision Date: Aug 18, 2017

1.Identification

1.1 GHS Product identifier

Product name difluoro-methyl-sulfanylidene-λ<sup>5</sup>-phosphane

1.2 Other means of identification

Product number -
Other names Methyl-monothiophosphonsaeure-difluorid

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:753-72-0 SDS

753-72-0Downstream Products

753-72-0Relevant academic research and scientific papers

New General Synthesis of Organophosphorus P-F Compounds via Reaction of Azolides of Phosphorus Acids with Acyl Fluorides: Novel Route to 2-Deoxynucleosidyl Phosphorofluoridates and Phosphorodifluoridates

Dabkowski, Wojciech,Michalski, Jan,Wasiak, Jacek,Cramer, Friedrich

, p. 817 - 820 (2007/10/02)

Tetra- and tri-coordinate P-N-imidazole derivatives and their structural analogous react smoothly with acyl fluorides to give the corresponding P-F compounds an almost quantitative yield.This method has been successfully applied to produce 2-deoxynucleosidyl phosphorofluoridates and phosphorodifluoridates.

ORGANOSILICON AND ORGANOPHOSPHORUS COMPOUNDS WITH PSEUDOHALIDE GROUPS 3. REACTIONS OF ALKOXYDIMETHYLSILYL CYANIDES WITH TETRACOORDINATED PHOSPHORUS HALIDES

Krolevets, A. A.,Antipova, V. V.,Petrovskii, P. V.,Martynov,I. V.

, p. 153 - 157 (2007/10/02)

The reactions of alkoxydimethylsilyl cyanides with some tetracoordinated phosphorus chlorides and fluorides were investigated.It was shown that the investigated reactions are realized primarily with the replacement of two halogen atoms by functional groups.The transformations of the phosphorus acid cyanides obtained with metal fluorides were studied. Keywords: silyl cyanides, phosphorus(IV) halides, substitution reactions, metal fluorides.

A NEW SYNTHESIS OF PHOSPHOROFLUORIDATES OF BIOLOGICAL INTEREST. THE REACTION OF PHOSPHOROAZOLIDES WITH BENZOYL FLUORIDE

Dabkowski, Wojciech,Cramer, Friedrich,Michalski, Jan

, p. 3561 - 3562 (2007/10/02)

Phosphoroazolides, including nucleoside derivatives, can be converted smoothly into the corresponding phosphorofluoridates by reaction with benzoyl fluoride.From these compounds oligonucleotides containing P-F instead of P-OH can be prepared.

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