<Suppliers Price>

1-Naphthalenesulfonyl chloride

Names

[ CAS No. ]:
85-46-1

[ Name ]:
1-Naphthalenesulfonyl chloride

[Synonym ]:
NAPHTHALENE-1-SULFONYL CHLORIDE
EINECS 201-609-6
NAPHTHOSULFOCHLORIDE
1-NAPHTHALENESULPHONYL CHLORIDE
Naphthalene sulfonyl chloride
1-Naphthylsulfonyl chloride
1-naphthalene sulfonyl chloride
NAPHTHALENE-1-SULPHONYL CHLORIDE
1-Chlorosulfonylnaphthalene
1-NAPTHALENESULFONIC CHLORIDE
MFCD00003984
1-naphthalenesulfonic acid chloride

Chemical & Physical Properties

[ Density]:
1.414 g/cm3

[ Boiling Point ]:
194-195 °C13 mm Hg(lit.)

[ Melting Point ]:
64-67 °C(lit.)

[ Molecular Formula ]:
C10H7ClO2S

[ Molecular Weight ]:
226.67900

[ Flash Point ]:
194-195°C/13mm

[ Exact Mass ]:
225.98600

[ PSA ]:
42.52000

[ LogP ]:
3.84810

[ Index of Refraction ]:
1.643

[ Water Solubility ]:
insoluble

MSDS

Safety Information

[ Symbol ]:

GHS05

[ Signal Word ]:
Danger

[ Hazard Statements ]:
H314

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

[ Personal Protective Equipment ]:
Eyeshields;Faceshields;full-face particle respirator type N100 (US);Gloves;respirator cartridge type N100 (US);type P1 (EN143) respirator filter;type P3 (EN 143) respirator cartridges

[ Hazard Codes ]:
C:Corrosive;

[ Risk Phrases ]:
R34

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

[ RIDADR ]:
UN 3261 8/PG 2

[ WGK Germany ]:
3

[ Packaging Group ]:
II

[ Hazard Class ]:
8

[ HS Code ]:
2904909090

Synthetic Route

Precursor & DownStream

Customs

[ HS Code ]: 2904909090

[ Summary ]:
HS:2904909090 sulphonated, nitrated or nitrosated derivatives of hydrocarbons, whether or not halogenated VAT:17.0% Tax rebate rate:9.0% Supervision conditions:none MFN tariff:5.5% General tariff:30.0%

Articles

1-Sulfonylindazoles as potent and selective 5-HT6 ligands.

Bioorg. Med. Chem. Lett. 19(9) , 2413-5, (2009)

As part of our continuing efforts to identify therapeutics for CNS diseases, such as schizophrenia and Alzheimer's disease (AD), we have been focused on the 5-HT(6) receptor in an attempt to identify ...

Aryl and arylmethyl C-glycosides through desulfitative stille and carbonylative stille cross-coupling of tinglycals and sulfonyl chlorides. Dubbaka SR, et al.

Synlett 2004(07) , 1235-38, (2004)

A simple method for the synthesis of O2, 5′-cyclodeoxyuridine. Tang SS and Roth JS.

Tetrahedron Lett. 9(17) , 2123-25, (1968)


More Articles


Related Compounds