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S-methyl tert-butyl(phenyl)phosphinothioate is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

76380-86-4

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76380-86-4 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 76380-86-4 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 7,6,3,8 and 0 respectively; the second part has 2 digits, 8 and 6 respectively.
Calculate Digit Verification of CAS Registry Number 76380-86:
(7*7)+(6*6)+(5*3)+(4*8)+(3*0)+(2*8)+(1*6)=154
154 % 10 = 4
So 76380-86-4 is a valid CAS Registry Number.

76380-86-4SDS

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 [tert-butyl(methylsulfanyl)phosphoryl]benzene

1.2 Other means of identification

Product number -
Other names S-methyl phenyl-t-butylphosphinothioate

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:76380-86-4 SDS

76380-86-4Relevant academic research and scientific papers

Reductive cleavage of the halogen-phosphorus and sulfur-phosphorus bonds with alkali metals

Stankiewicz, Marek,Nycz, Jacek,Rachon, Janusz

, p. 330 - 339 (2007/10/03)

The reduction of thiophosphorus acid chlorides with alkali metals (Na, K) in liq. NH3/THF solution, potassium anthracenide, and potassium napththalenide was investigated. It was found that these types of phosphorus compounds easily undergo reduction to 〉P-S- anions. It was also demonstrated that 〉P-O- and 〉P-S- anions as well very efficiently undergo sulfurization with elementary sulfur in liquid ammonia to yield 〉P(O)S- and 〉P(S)S- anions, respectively.

A new, stereoselective interconversion of phosphinothio-phosphinoseleno compounds, reduction of phosphinoseleno derivatives and retro pishchimuka rearrangement based on methylthio- and methylselenophosphonium salts chemistry

Omelanczuk, Jan

, p. 8887 - 8898 (2007/10/02)

The interconversion of thiono- into seleno compounds was found to proceed with retention of the configuration at phosphorus and the mechanistic course of this process has been proposed. The isomerization reaction of phosphinothiolates into thiono-isomers via the phosphonium salts has been developed and considered as the "retro Pishchimuka" rearrangement.

Reaction of Thiolo and Seleno Esters of Phosphorus Acids with Halogens. 1. Stereochemical and 31P NMR Studies of Reaction of S-Methyl tert-Butylphenylphosphinothiolate with Elemental Chlorine and Sulfuryl Chloride

Krawiecka, B.,Michalski, J.,Wojna-Tadeusiak, E.

, p. 4201 - 4208 (2007/10/02)

Reaction of S-methyl tert-butylphenylphosphinothiolate (4) with elemental chlorine and sulfuryl chloride involves chlorolysis of the P-S bond and formation of the tert-butylphenylphosphinochloridate 5.It is demonstrated here that the stereoselectivity of

The Proton Magnetic Resonance Spectra of Chiral Phosphinate Esters. Chemical Shift Non-equivalence of Enantiomers induced by Optically Active Phosphinothioic Acids

Harger, Martin J. P.

, p. 1505 - 1511 (2007/10/02)

The 1H n.m.r. spectrum of racemic methyl methylphenylphosphinate recorded in CCl4 solution in the presence of 1 mol. equiv. of (+)-(R)-phenyl-t-butylphosphinothioic acid or (-)-(S)-methylphenylphosphinothioic acid contains well separated P-m

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