556165
3-Methoxybenzenesulfonyl chloride
96%
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About This Item
Linear Formula:
CH3OC6H4SO2Cl
CAS Number:
Molecular Weight:
206.65
NACRES:
NA.22
PubChem Substance ID:
UNSPSC Code:
12352100
MDL number:
Assay:
96%
Product Name
3-Methoxybenzenesulfonyl chloride, 96%
InChI
1S/C7H7ClO3S/c1-11-6-3-2-4-7(5-6)12(8,9)10/h2-5H,1H3
SMILES string
COc1cccc(c1)S(Cl)(=O)=O
InChI key
JHJKSEKUZNJKGO-UHFFFAOYSA-N
assay
96%
refractive index
n20/D 1.5560 (lit.)
density
1.460 g/mL at 25 °C (lit.)
Quality Level
Related Categories
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.
signalword
Danger
hcodes
Hazard Classifications
Eye Dam. 1 - Skin Corr. 1B
Storage Class
8A - Combustible corrosive hazardous materials
wgk
WGK 3
flash_point_f
Not applicable
flash_point_c
Not applicable
ppe
Faceshields, Gloves, Goggles, type ABEK (EN14387) respirator filter
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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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