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Key Documents

556165

Sigma-Aldrich

3-Methoxybenzenesulfonyl chloride

96%

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About This Item

Linear Formula:
CH3OC6H4SO2Cl
CAS Number:
Molecular Weight:
206.65
MDL number:
UNSPSC Code:
12352100
PubChem Substance ID:
NACRES:
NA.22

Quality Level

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

Signal Word

Danger

Hazard Statements

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

Certificates of Analysis (COA)

Search for Certificates of Analysis (COA) by entering the products Lot/Batch Number. Lot and Batch Numbers can be found on a product’s label following the words ‘Lot’ or ‘Batch’.

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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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