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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)-

3-Thiophenesulfonyl chloride, 2,5-dimethyl-

Cc1sc(c(c1)S(=O)(=O)Cl)C Request for Quotation
Chemical Name: 3-Thiophenesulfonyl chloride, 2,5-dimethyl-
CAS Number: 97272-04-3
Product Number: AG005ZVE(AGN-PC-0KKZPZ)
Synonyms:
MDL No:
Molecular Formula: C6H7ClO2S2
Molecular Weight: 210.7016

Identification/Properties

Properties
MP:
120-122 °C
BP:
298.6 °C at 760 mmHg
Form:
Solid
Computed Properties
Molecular Weight:
210.69g/mol
XLogP3:
2.4
Hydrogen Bond Donor Count:
0
Hydrogen Bond Acceptor Count:
3
Rotatable Bond Count:
1
Exact Mass:
209.958g/mol
Monoisotopic Mass:
209.958g/mol
Topological Polar Surface Area:
70.8A^2
Heavy Atom Count:
11
Formal Charge:
0
Complexity:
232
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

GHS Pictogram:
Signal Word:
Danger
UN#:
3265
Hazard Statements:
H314
Precautionary Statements:
P260-P264-P280-P301+P330+P331-P303+P361+P353-P304+P340-P305+P351+P338-P310-P321-P363-P405-P501
Class:
8
Packing Group:
Ⅲ

NMR Spectrum

Other Analytical Data

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Chemical Structure


2,5-Dimethylthiophene-3-sulfonyl chloride, also known as $name$, is a highly versatile compound widely used in chemical synthesis. This reagent is predominantly employed as a key building block in the pharmaceutical industry, where its unique structure and reactivity enable the efficient synthesis of various bioactive molecules. Its sulfonate moiety acts as an excellent leaving group, facilitating nucleophilic substitution reactions to introduce functional groups at specific positions in organic molecules. Furthermore, the presence of the thiophene ring imparts desirable electronic properties to the compounds synthesized, making them valuable intermediates in drug discovery and development processes. Additionally, $name$ has found application in the synthesis of agrochemicals, dyes, and advanced materials, showcasing its significance across different sectors of the chemical industry.