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556165

Sigma-Aldrich

3-Methoxybenzenesulfonyl chloride

96%

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About This Item

Linear Formula:
CH3OC6H4SO2Cl
CAS Number:
10130-74-2
Molecular Weight:
206.65
MDL number:
MFCD01318155
UNSPSC Code:
12352100
PubChem Substance ID:
24879527
NACRES:
NA.22

Assay

96%

refractive index

n20/D 1.5560 (lit.)

density

1.460 g/mL at 25 °C (lit.)

SMILES string

COc1cccc(c1)S(Cl)(=O)=O

InChI

1S/C7H7ClO3S/c1-11-6-3-2-4-7(5-6)12(8,9)10/h2-5H,1H3

InChI key

JHJKSEKUZNJKGO-UHFFFAOYSA-N

Application

3-Methoxybenzenesulfonyl chloride may be used to synthesize 3-(4-phenylpiperazin-1yl) sulfonyls and N-(1-(4-methoxybenzyl)-3-cyclopropyl-1Hpyrazol-5-yl)-3-methoxybenzenesulfonamide.

Pictograms

Corrosion
GHS05

Signal Word

Danger

Hazard Statements

H314

Hazard Classifications

Eye Dam. 1 - Skin Corr. 1B

Storage Class Code

8A - Combustible corrosive hazardous materials

WGK

WGK 3

Flash Point(F)

Not applicable

Flash Point(C)

Not applicable

Personal Protective Equipment

dust mask type N95 (US), Eyeshields, Gloves

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Certificates of Analysis (COA)

Lot/Batch Number
STBK5504
STBG4093V
STBC5482V
STBB7223V
STBB7223

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Addressing cytotoxicity of 1, 4-biphenyl amide derivatives: Discovery of new potent and selective 17b-hydroxysteroid dehydrogenase type 2 inhibitors.
Gargano EM, et al.
Bioorganic & Medicinal Chemistry Letters (2015)
Hanumegowda Raju et al.
Recent patents on anti-cancer drug discovery, 6(2), 186-195 (2011-01-21)
In search of synthetic chemotherapeutic substances capable of inhibiting, retarding, or reversing the process of multistage carcinogenesis, we synthesised a series of novel 1-(4-methoxybenzyl)-3-cyclopropyl-1H-pyrazol-5-amine derivatives 9(a-h) by a nucleophilic substitution reaction and characterized by (1)H and (13)C nuclear magnetic resonance

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