1-Chloroadamantane
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
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)
MSDS
- Language:English Provider:1-Adamantyl chloride
- Language:English Provider:ACROS
- Language:English Provider:SigmaAldrich
- Language:English Provider:ALFA
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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1-Chloroadamantane(935-56-8)Related Product Information
- Calcium chloride
- Benzyl chloride
- Adamantane
- Sodium chloride
- 1-Adamantanecarboxylic acid
- Choline chloride
- Ammonium chloride
- Decane
- Mepiquat chloride
- Polyvinyl chloride
- Methylene Chloride
- 5-CHLORO-2-ADAMANTANONE
- 3-CHLOROADAMANTANE-1-CARBOXYLIC ACID,3-CHLOROADAMANTANE CARBOXYLIC ACID
- 2-CHLOROADAMANTANE
- 1-Aminoadamantane-2,2,2′,2′,2″,2″-d6
- Amantadine
- 1-Adamantanamine hydrochloride
- 1-CHLOROADAMANTANE-D15