<Suppliers Price>

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)


More Articles


Related Compounds

The content on this webpage is sourced from various professional data sources. If you have any questions or concerns regarding the content, please feel free to contact service1@chemsrc.com.