Phosphinothioic chloride, dimethyl-

Base Information

• Chemical Name: Phosphinothioic chloride, dimethyl-
• CAS No.: 993-12-4
• Molecular Formula: C2H6ClPS
• Molecular Weight: 128.562
• Hs Code.: 2930909090
• European Community (EC) Number: 213-606-7
• UNII: TQ4MR8AA6Y
• DSSTox Substance ID: DTXSID6075439
• Nikkaji Number: J298.592F
• Wikidata: Q82003341
• Mol file: 993-12-4.mol

Synonyms:993-12-4;Dimethylphosphinothioic chloride;Phosphinothioic chloride, dimethyl-;Dimethylthiophosphinoyl Chloride;Dimethylthiophosphinic chloride;Dimethylphosphinothioyl chloride;TQ4MR8AA6Y;Chlorodimethylphosphine sulfide;chloro-dimethyl-sulfanylidene-lambda5-phosphane;EINECS 213-606-7;C2H6ClPS;UNII-TQ4MR8AA6Y;C2-H6-Cl-P-S;dimethylthiophosphinyl chloride;SCHEMBL1250877;DTXSID6075439;MFCD00014454;AKOS015852450;D2159;FT-0633210;T71511;Dimethyl thiophosphoryl chloride [UN2267] [Poison]

Chemical Property of Phosphinothioic chloride, dimethyl-

Chemical Property:

• Appearance/Colour: clear colorless to light yellow liquid
• Vapor Pressure: 11.3mmHg at 25°C
• Refractive Index: 1.538-1.541
• Boiling Point: 131.6 °C at 760 mmHg
• Flash Point: 33.4 °C
• PSA: 41.90000
• Density: 1.224 g/cm³
• LogP: 2.52990
• Storage Temp.: Refrigerator
• XLogP3: 1.9
• Hydrogen Bond Donor Count: 0
• Hydrogen Bond Acceptor Count: 1
• Rotatable Bond Count: 0
• Exact Mass: 127.9616361
• Heavy Atom Count: 5
• Complexity: 64

Purity/Quality:

98%,99%, ^*data from raw suppliers

Dimethylthiophosphinoyl Chloride ^*data from reagent suppliers

Safty Information:

• Pictogram(s): C
• Hazard Codes: C
• Statements: 34-29-20/21/22
• Safety Statements: 8-45-36/37/39-26

MSDS Files:

SDS file from LookChem

Useful:

• Canonical SMILES: CP(=S)(C)Cl

Technology Process of Phosphinothioic chloride, dimethyl-

There total 3 articles about Phosphinothioic chloride, dimethyl- which guide to synthetic route it. The literature collected by LookChem mainly comes from the sharing of users and the free literature resources found by Internet computing technology. We keep the original model of the professional version of literature to make it easier and faster for users to retrieve and use. At the same time, we analyze and calculate the most feasible synthesis route with the highest yield for your reference as below:

synthetic route:

Reference yield:

→ dimethylphosphinothioic chloride (993-12-4)

Guidance literature:

With antimony (v) sulfide; potassium chloride;

Reference yield:

chlorodimethylphosphine (811-62-1) → dimethylphosphinothioic chloride (993-12-4)

Guidance literature:

With sulfur;

Reference yield:

→ dimethylphosphinothioic chloride (993-12-4)

Guidance literature:

DOI:10.1002/hlca.19640470805 DOI:10.1016/0022-1902(62)80251-6 DOI:10.1002/hlca.19630460620 DOI:10.1021/ja00987a026 DOI:10.1002/zaac.19683600309 DOI:10.1007/BF00925893 DOI:10.1016/0022-1902(61)80463-6 DOI:10.1002/hlca.19640470106 DOI:10.1021/ja00965a027

upstream raw materials:

chlorodimethylphosphine

Downstream raw materials:

O-(4-chlorophenyl)dimethylphosphinothioate

N-Dimethylthiophosphinyl-N'-benzoyl-hydrazin

p-chlorophenyldimethylphosphine sulfide

1-(Dimethyl-phosphinothioyl)-4-methoxy-benzene