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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)-

Carbonochloridic acid, 4-methylphenyl ester

ClC(=O)Oc1ccc(cc1)C Request for Quotation
Chemical Name: Carbonochloridic acid, 4-methylphenyl ester
CAS Number: 937-62-2
Product Number: AG003U1B(AGN-PC-0JL9LR)
Synonyms:
MDL No:
Molecular Formula: C8H7ClO2
Molecular Weight: 170.59298

Identification/Properties

Computed Properties
Molecular Weight:
170.592g/mol
XLogP3:
3.2
Hydrogen Bond Donor Count:
0
Hydrogen Bond Acceptor Count:
2
Rotatable Bond Count:
2
Exact Mass:
170.013g/mol
Monoisotopic Mass:
170.013g/mol
Topological Polar Surface Area:
26.3A^2
Heavy Atom Count:
11
Formal Charge:
0
Complexity:
139
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


p-Tolylchloroformate is a versatile chemical reagent widely used in organic synthesis for various transformations. Also known as 4-chloroformyloxytoluene, this compound has a reactive functional group that enables it to participate in a range of synthetic reactions.One of the key applications of p-Tolylchloroformate is as a carbonylating agent in the formation of esters and carbamates. It can react with alcohols and amines to selectively introduce the p-tolylcarbonyl group onto the nucleophilic oxygen or nitrogen atom, leading to the formation of esters or carbamates, respectively. This reaction is commonly used in the synthesis of pharmaceuticals, agrochemicals, and fine chemicals.In addition, p-Tolylchloroformate can also be employed in the protection of alcohols and amines in organic synthesis. By converting hydroxyl or amino groups into their corresponding carbonate derivatives using p-Tolylchloroformate, these functional groups can be temporarily shielded from unwanted reactions and subsequently deprotected under mild conditions when needed.Furthermore, p-Tolylchloroformate serves as an important building block in the preparation of peptide-based compounds and other bioactive molecules. Its versatile reactivity and compatibility with a variety of functional groups make it a valuable tool in the design and synthesis of complex chemical structures for various applications in medicinal chemistry and materials science.Overall, p-Tolylchloroformate plays a crucial role in chemical synthesis by enabling the efficient construction of diverse organic molecules with precision and control, making it a valuable asset for researchers and chemists in the field of organic chemistry.