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3-Methoxybenzenesulfonyl chloride

Names

[ CAS No. ]:
10130-74-2

[ Name ]:
3-Methoxybenzenesulfonyl chloride

[Synonym ]:
3-Methoxybenzene-1-sulfonyl chloride
3-Methoxybenzenesulfonyl chloride
Benzenesulfonyl chloride, 3-methoxy-
MFCD01318155
3-Methoxybenzenesulphonyl chloride
WSGR CO1

Chemical & Physical Properties

[ Density]:
1.4±0.1 g/cm3

[ Boiling Point ]:
304.5±25.0 °C at 760 mmHg

[ Molecular Formula ]:
C7H7ClO3S

[ Molecular Weight ]:
206.647

[ Flash Point ]:
138.0±23.2 °C

[ Exact Mass ]:
205.980438

[ PSA ]:
51.75000

[ LogP ]:
2.34

[ Vapour Pressure ]:
0.0±0.6 mmHg at 25°C

[ Index of Refraction ]:
1.536

Safety Information

[ Symbol ]:

GHS05

[ Signal Word ]:
Danger

[ Hazard Statements ]:
H314

[ Precautionary Statements ]:
P280-P305 + P351 + P338-P310

[ Personal Protective Equipment ]:
Faceshields;full-face respirator (US);Gloves;Goggles;multi-purpose combination respirator cartridge (US);type ABEK (EN14387) respirator filter

[ Hazard Codes ]:
C:Corrosive;

[ Risk Phrases ]:
R34

[ Safety Phrases ]:
S26-S36/37/39-S45-S39-S37-S36

[ RIDADR ]:
UN 3265 8/PG 2

[ WGK Germany ]:
3

[ Packaging Group ]:
II

[ Hazard Class ]:
8

[ HS Code ]:
2909309090

Synthetic Route

Precursor & DownStream

Customs

[ HS Code ]: 2909309090

[ Summary ]:
2909309090 other aromatic ethers and their halogenated, sulphonated, nitrated or nitrosated derivatives VAT:17.0% Tax rebate rate:9.0% Supervision conditions:none MFN tariff:5.5% General tariff:30.0%

Articles

Synthesis, characterization and in-vitro antiproliferative effects of novel 5-amino pyrazole derivatives against breast cancer cell lines.

Recent Pat. Anticancer. Drug Discov. 6(2) , 186-95, (2011)

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-cyclo...

Addressing cytotoxicity of 1, 4-biphenyl amide derivatives: Discovery of new potent and selective 17b-hydroxysteroid dehydrogenase type 2 inhibitors. Gargano EM, et al.

Bioorg. Med. Chem. Lett. , (2015)


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Related Compounds