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Brc1cnc(nc1)C
Pyrimidine, 5-bromo-2-methyl-
CCCP1(=O)OP(=O)(CCC)OP(=O)(O1)CCC
1,3,5,2,4,6-Trioxatriphosphorinane, 2,4,6-tripropyl-, 2,4,6-trioxide
CC1(C)OB(OC1(C)C)B1OC(C(O1)(C)C)(C)C
2,2'-Bi-1,3,2-dioxaborolane, 4,4,4',4',5,5,5',5'-octamethyl-
O=C(C=Cc1ccccc1)C=Cc1ccccc1.O=C(C=Cc1ccccc1)C=Cc1ccccc1.O=C(C=Cc1ccccc1)C=Cc1ccccc1.[Pd].[Pd]
Tris(dibenzylideneacetone)dipalladium
C1CCC(CC1)P(C1CCCCC1)C1CCCCC1.Cc1cc(C)c(c(c1)C)N1CCN(C1=[Ru](=Cc1ccccc1)(Cl)Cl)c1c(C)cc(cc1C)C
Ruthenium,[1,3-bis(2,4,6-trimethylphenyl)-2-imidazolidinylidene]dichloro(phenylmethylene)(tricyclohexylphosphine)-, (SP-5-41)-

Carbonochloridothioic acid, O-(4-methylphenyl) ester

ClC(=S)Oc1ccc(cc1)C Request for Quotation
Chemical Name: Carbonochloridothioic acid, O-(4-methylphenyl) ester
CAS Number: 937-63-3
Product Number: AG003U1C(AGN-PC-0JL9LS)
Synonyms:
MDL No:
Molecular Formula: C8H7ClOS
Molecular Weight: 186.65858

Identification/Properties

Computed Properties
Molecular Weight:
186.653g/mol
XLogP3:
3.8
Hydrogen Bond Donor Count:
0
Hydrogen Bond Acceptor Count:
2
Rotatable Bond Count:
2
Exact Mass:
185.991g/mol
Monoisotopic Mass:
185.991g/mol
Topological Polar Surface Area:
41.3A^2
Heavy Atom Count:
11
Formal Charge:
0
Complexity:
141
Isotope Atom Count:
0
Defined Atom Stereocenter Count:
0
Undefined Atom Stereocenter Count:
0
Defined Bond Stereocenter Count:
0
Undefined Bond Stereocenter Count:
0
Covalently-Bonded Unit Count:
1
Compound Is Canonicalized:
Yes

Safety Information

NMR Spectrum

Other Analytical Data

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Chemical Structure


In chemical synthesis, p-tolyl chlorothionoformate serves as a versatile reagent for the preparation of various sulfur-containing compounds. It can be used as a chlorothionating agent to introduce both chlorine and sulfur functionalities into organic molecules. This reagent enables the selective functionalization of substrates to form valuable intermediates in the synthesis of pharmaceuticals, agrochemicals, and other fine chemicals. Additionally, p-tolyl chlorothionoformate's compatibility with a wide range of functional groups makes it a valuable tool in the development of efficient synthetic routes. Its ability to control regioselectivity and stereoselectivity in chemical reactions further enhances its utility in complex molecule synthesis. By facilitating the construction of sulfur-containing motifs, p-tolyl chlorothionoformate contributes significantly to the diversification of molecular structures, enabling the creation of new compounds with enhanced biological or physical properties.