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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)-

Benzenesulfonyl chloride, 4-(1-methylethoxy)-

CC(Oc1ccc(cc1)S(=O)(=O)Cl)C Request for Quotation
Chemical Name: Benzenesulfonyl chloride, 4-(1-methylethoxy)-
CAS Number: 98995-40-5
Product Number: AG003LL8(AGN-PC-03O247)
Synonyms:
MDL No:
Molecular Formula: C9H11ClO3S
Molecular Weight: 234.6998

Identification/Properties

Properties
MP:
30-35 °C
BP:
333.7°C at 760 mmHg
Storage:
Inert atmosphere;2-8℃;
Form:
Solid
Stability:
Moisture Sensitive
Computed Properties
Molecular Weight:
234.694g/mol
XLogP3:
2.7
Hydrogen Bond Donor Count:
0
Hydrogen Bond Acceptor Count:
3
Rotatable Bond Count:
3
Exact Mass:
234.012g/mol
Monoisotopic Mass:
234.012g/mol
Topological Polar Surface Area:
51.8A^2
Heavy Atom Count:
14
Formal Charge:
0
Complexity:
260
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#:
3261
Hazard Statements:
H314-H318
Precautionary Statements:
P280-P305+P351+P338-P310
Class:
8
Packing Group:
Ⅱ

NMR Spectrum

Other Analytical Data

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Chemical Structure


4-Isopropoxybenzene-1-sulfonyl chloride, also known as 4-Isopropoxybenzenesulfonyl chloride or p-Toluenesulfonyl chloride, is a versatile and valuable reagent in chemical synthesis. This compound is commonly used as a sulfonylating agent in organic chemistry reactions. By utilizing 4-Isopropoxybenzene-1-sulfonyl chloride, chemists can introduce sulfonyl groups onto various organic molecules, providing a means of functionalizing and modifying their chemical structures. The sulfonyl chloride group in this compound is highly reactive, enabling it to react with nucleophiles such as amines, alcohols, and thiols to form sulfonamides, sulfonates, and sulfides, respectively. Additionally, 4-Isopropoxybenzene-1-sulfonyl chloride is utilized in the synthesis of pharmaceuticals, advanced materials, and agrochemicals due to its ability to selectively activate specific functional groups in complex molecules. Its versatility and reactivity make it a valuable tool in the arsenal of synthetic chemists seeking to create novel compounds with tailored properties.