Basic information Safety Supplier Related

6-Chloroindole

Basic information Safety Supplier Related

6-Chloroindole Basic information

Product Name:
6-Chloroindole
Synonyms:
  • 6-chloro-1H-indole(SALTDATA: FREE)
  • 6-chloroindole 17422-32-2
  • NSC 58083
  • 6-Chloroindole, 97+%
  • 6-Chloroindole in stock Factory
  • 1H-Indole, 6-chloro-
  • 1H-Indole,6-chloro-(9CI)
  • TIMTEC-BB SBB004059
CAS:
17422-33-2
MF:
C8H6ClN
MW:
151.59
EINECS:
241-449-4
Product Categories:
  • Indoles
  • Heterocycle-Indole series
  • Building Blocks
  • C7 to C10
  • C7 to C9
  • Chemical Synthesis
  • INDOLE
  • Simple Indoles
  • Indole Derivatives
  • Halogenated Heterocycles
  • Heterocyclic Building Blocks
  • IndolesBuilding Blocks
  • Halogenated Heterocycles
  • Heterocyclic Building Blocks
  • blocks
  • IndolesOxindoles
  • Indole/indoline/oxindole
  • Indole and Indoline
  • Indoles and derivatives
  • bc0001
Mol File:
17422-33-2.mol
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6-Chloroindole Chemical Properties

Melting point:
87-90 °C (lit.)
Boiling point:
248.91°C (rough estimate)
Density 
1.1976 (rough estimate)
refractive index 
1.5437 (estimate)
storage temp. 
Keep in dark place,Inert atmosphere,Room temperature
solubility 
slightly soluble
form 
Crystalline Powder
pka
16.10±0.30(Predicted)
color 
Beige
Water Solubility 
slightly soluble
BRN 
112345
Stability:
Store in Refrigerator
CAS DataBase Reference
17422-33-2(CAS DataBase Reference)
NIST Chemistry Reference
6-Chloroindole(17422-33-2)
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Safety Information

Hazard Codes 
Xi
Risk Statements 
36/37/38
Safety Statements 
22-24/25-37/39-26-36
WGK Germany 
3
Hazard Note 
Irritant
TSCA 
A
HS Code 
29339990

MSDS

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6-Chloroindole Usage And Synthesis

Chemical Properties

Light Orange Powder

Uses

6-Chloroindole (cas# 17422-33-2) is a compound useful in organic synthesis.

Definition

ChEBI: 6-Chloroindole is a member of indoles.

Synthesis Reference(s)

The Journal of Organic Chemistry, 55, p. 580, 1990 DOI: 10.1021/jo00289a036

General Description

6-Chloroindole, when added to Claviceps purpurea, produced the corresponding substituted L-tryptophan.

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