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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)-

Carbamic acid, [(4-methylphenyl)sulfonyl]-, methyl ester

COC(=O)NS(=O)(=O)c1ccc(cc1)C Request for Quotation
Chemical Name: Carbamic acid, [(4-methylphenyl)sulfonyl]-, methyl ester
CAS Number: 14437-03-7
Product Number: AG001JFF(AGN-PC-0JLV38)
Synonyms:
MDL No:
Molecular Formula: C9H11NO4S
Molecular Weight: 229.2529

Identification/Properties

Properties
MP:
107-109°C
Storage:
Keep in dry area;Room Temperature;
Form:
Solid
Computed Properties
Molecular Weight:
229.25g/mol
XLogP3:
0.8
Hydrogen Bond Donor Count:
1
Hydrogen Bond Acceptor Count:
4
Rotatable Bond Count:
3
Exact Mass:
229.041g/mol
Monoisotopic Mass:
229.041g/mol
Topological Polar Surface Area:
80.8A^2
Heavy Atom Count:
15
Formal Charge:
0
Complexity:
312
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


Methyl tosylcarbamate, also known as MTC, is a versatile compound widely used in chemical synthesis for its ability to act as a protecting group in organic reactions. This compound plays a crucial role in organic chemistry by selectively masking certain functional groups within a molecule, thereby allowing specific transformations to occur without unwanted side reactions. In the field of synthetic chemistry, MTC is particularly valued for its compatibility with a variety of reaction conditions and its ease of removal after the desired chemical manipulations have been completed. By incorporating MTC into synthetic pathways, chemists can efficiently and selectively modify complex molecules to produce a diverse range of target compounds for pharmaceuticals, agrochemicals, materials science, and other industrial applications.