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2-Naphthalenesulfonyl chloride

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2-Naphthalenesulfonyl chloride Basic information

Product Name:
2-Naphthalenesulfonyl chloride
Synonyms:
  • NAPHTHALENE-BETA-SULFONYL CHLORIDE
  • NAPHTHALENE-2-SULFONYL CHLORIDE
  • NAPHTHALENE-2-SULPHONYL CHLORIDE
  • 2-NAPHTHALENESULFONYL CHLORIDE
  • AKOS B022434
  • ART-CHEM-BB B022434
  • BETA-NAPHTHALENE SULFONYL CHLORIDE
  • 2-Naphthalenylsulfonyl chloride
CAS:
93-11-8
MF:
C10H7ClO2S
MW:
226.68
EINECS:
202-219-9
Product Categories:
  • Organic Building Blocks
  • Sulfonyl Halides
  • Sulfur Compounds
  • Building Blocks
  • Chemical Synthesis
  • Indolines ,Indoles ,Indazoles
  • Organic Building Blocks
  • Sulfonyl Halides
  • Sulfur Compounds
  • Indazoles
Mol File:
93-11-8.mol
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2-Naphthalenesulfonyl chloride Chemical Properties

Melting point:
74-76 °C (lit.)
Boiling point:
147.7 °C/0.6 mmHg (lit.)
Density 
1.3661 (estimate)
vapor pressure 
0.004Pa at 25℃
Flash point:
200-202°C/13mm
storage temp. 
Keep in dark place,Sealed in dry,Room Temperature
solubility 
soluble in Toluene
form 
Powder
color 
Light yellow to beige
Water Solubility 
insoluble
Sensitive 
Moisture Sensitive
BRN 
641898
InChIKey
OPECTNGATDYLSS-UHFFFAOYSA-N
LogP
2.2 at 25℃
CAS DataBase Reference
93-11-8(CAS DataBase Reference)
NIST Chemistry Reference
2-Naphthalenesulfonyl chloride(93-11-8)
EPA Substance Registry System
2-Naphthalenesulfonyl chloride (93-11-8)
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Safety Information

Hazard Codes 
C
Risk Statements 
34
Safety Statements 
26-36/37/39-45-27
RIDADR 
UN 3261 8/PG 2
WGK Germany 
3
21
TSCA 
Yes
HazardClass 
8
PackingGroup 
II
HS Code 
29049020

MSDS

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2-Naphthalenesulfonyl chloride Usage And Synthesis

Chemical Properties

LIGHT YELLOW TO BEIGE POWDER

Uses

2-Naphthalenesulfonyl chloride was employed as capping reagent for primary amine to convert histamine to a selective histamine H3-receptor antagonist. It was used for pre-column derivatization during the high-performance liquid chromatographic assay of neomycin sulfate.

Flammability and Explosibility

Not classified

Purification Methods

Distil the chloride in a vacuum and/or recrystallise it (twice) from *benzene/pet ether (1:1 v/v). Purify it as the 1-sulfonyl chloride above. [Fierz-Davaid & Weissenbach Helv Chim Acta 3 2312 1920.] The sulfonamide has m 217o (from EtOH). [Beilstein 11 III 399, 11 IV 529.]

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