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1-Chloroadamantane

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1-Chloroadamantane Basic information

Product Name:
1-Chloroadamantane
Synonyms:
  • 1-ChloroadaMantane SynonyMs 1-AdaMantyl chloride
  • 1-chloroadamanane
  • 1-Chloroadamantane 98%
  • Amantadine Related Compound A
  • LABOTEST-BB LT00033850
  • 3-Chloroadamantane
  • 7]decane,1-chloro-tricyclo[3.3.1.1
  • Adamantyl chloride
CAS:
935-56-8
MF:
C10H15Cl
MW:
170.68
EINECS:
213-305-0
Product Categories:
  • Chemical Synthesis
  • Halogenated Hydrocarbons
  • Adamantane derivatives
  • Adamantanes
  • Alkyl
  • Organic Building Blocks
  • Halogenated Hydrocarbons
  • Organic Building Blocks
  • Building Blocks
Mol File:
935-56-8.mol
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1-Chloroadamantane Chemical Properties

Melting point:
165-166 °C(lit.)
Boiling point:
211.58°C (rough estimate)
Density 
1.0492 (rough estimate)
refractive index 
1.6012 (estimate)
storage temp. 
2-8°C
solubility 
DMSO, Methanol (Slightly)
form 
Crystalline
color 
Off-White
Water Solubility 
Poorly soluble in water. Soluble in hydrocarbons. But readily soluble in nonpolar organic solvents.
Stability:
Light Sensitive
InChI
InChI=1S/C10H15Cl/c11-10-4-7-1-8(5-10)3-9(2-7)6-10/h7-9H,1-6H2
InChIKey
OZNXTQSXSHODFR-UHFFFAOYSA-N
SMILES
C12(Cl)CC3CC(CC(C3)C1)C2
CAS DataBase Reference
935-56-8(CAS DataBase Reference)
NIST Chemistry Reference
Adamantane, 1-chloro-(935-56-8)
EPA Substance Registry System
Tricyclo[3.3.1.13,7]decane, 1-chloro- (935-56-8)
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Safety Information

Hazard Codes 
Xi
Risk Statements 
36/37/38
Safety Statements 
24/25
WGK Germany 
3
TSCA 
Yes
HS Code 
29035980

MSDS

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1-Chloroadamantane Usage And Synthesis

Chemical Properties

white to light grey adhering crystalline solid or

Uses

1-Chloroadamantane, an adamantane derivative shown to exhibit virucidal activity against the Newcastle disease virus in chick embryo fibroblasts. (Adamantane EP Impurity A)

Uses

1-Chloroadamantane was employed as precursor for the synthesis of perfluoroadmantane derivatives via aerosol direct fluorination.

Synthesis Reference(s)

Synthetic Communications, 19, p. 1697, 1989 DOI: 10.1080/00397918908051068

General Description

An unusual zwitterionic diradical intermediate complex was generated during the photoinduced electron-transfer substitution reaction between 1-chloroadamantane and tert-butylamine system in a hydrocarbon glass.

Purification Methods

Crystallise the chloride from aqueous MeOH and sublime it at 100o/12torr. It also crystallises from MeOH at -70o. [Stetter et al. Chem Ber 92 1629 1959, Schleyer & Nicholas J Am Chem Soc 83 2700 1961, Beilstein 5 IV 469.]

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