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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)-

1-Propanesulfonyl chloride, 2-methyl-

CC(CS(=O)(=O)Cl)C Request for Quotation
Chemical Name: 1-Propanesulfonyl chloride, 2-methyl-
CAS Number: 35432-36-1
Product Number: AG0033EF(AGN-PC-0JNGSK)
Synonyms:
MDL No:
Molecular Formula: C4H9ClO2S
Molecular Weight: 156.6311

Identification/Properties

Properties
BP:
190°C at 760 mmHg
Storage:
Inert atmosphere;2-8℃;
Form:
Liquid
Stability:
Moisture Sensitive
Refractive Index:
n20/D 1.454(lit.)
Computed Properties
Molecular Weight:
156.624g/mol
XLogP3:
1.7
Hydrogen Bond Donor Count:
0
Hydrogen Bond Acceptor Count:
2
Rotatable Bond Count:
2
Exact Mass:
156.001g/mol
Monoisotopic Mass:
156.001g/mol
Topological Polar Surface Area:
42.5A^2
Heavy Atom Count:
8
Formal Charge:
0
Complexity:
142
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


2-Methylpropane-1-sulfonyl chloride, also known as t-Butylsulfonyl chloride, is a versatile compound widely used in chemical synthesis. Its application in organic chemistry primarily involves its role as a sulfonylating reagent. When 2-Methylpropane-1-sulfonyl chloride is introduced to a reaction mixture, it can act as a sulfonyl chloride source, facilitating sulfonation reactions.One common application of 2-Methylpropane-1-sulfonyl chloride is in the synthesis of sulfonamides. By reacting with amines, this compound can form sulfonamide derivatives, which are valuable intermediates in pharmaceutical and agrochemical industries. The sulfonyl group enhances the reactivity and stability of the resulting products, making them useful building blocks for further chemical transformations.Furthermore, 2-Methylpropane-1-sulfonyl chloride can also be employed to introduce sulfonyl protecting groups in organic synthesis. By selectively reacting with hydroxyl or amino groups in target molecules, this compound can mask reactive functionalities, providing temporary protection during multi-step synthesis processes. Upon completion of the desired reactions, the sulfonyl group can be easily removed under specific conditions to reveal the original functional groups.Overall, 2-Methylpropane-1-sulfonyl chloride serves as a valuable tool in chemical synthesis, enabling the efficient and precise manipulation of functional groups in organic molecules. Its versatility and reactivity make it a key component in the arsenal of synthetic chemists seeking to design and create complex organic compounds for various applications.