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Bornane, also known as norbornane, is a bicyclic organic compound belonging to the class of hydrocarbons. It is a colorless, crystalline substance with a camphor-like odor. Bornane is characterized by its low solubility in water and relative stability under normal conditions, making it a versatile and important chemical in various industrial and research applications.

464-15-3

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464-15-3 Usage

Uses

Used in Pharmaceutical Synthesis:
Bornane is used as a starting material in the synthesis of various pharmaceuticals. Its unique structure and properties make it a valuable component in the development of new drugs and medications.
Used in Fragrance and Flavor Production:
Bornane is utilized as a starting material in the production of fragrances and flavors. Its camphor-like odor and versatility contribute to the creation of a wide range of scents and tastes in the fragrance and flavor industries.
Used as a Chiral Auxiliary in Asymmetric Synthesis:
Bornane is employed as a chiral auxiliary in asymmetric synthesis. Its unique stereochemistry allows for the selective synthesis of enantiomers, which is crucial in the development of chiral drugs and other chiral compounds.
Used in the Preparation of Polycyclic Compounds:
Bornane serves as a building block for the preparation of polycyclic compounds. Its bicyclic structure and chemical properties make it an ideal component for constructing complex polycyclic systems, which are important in various chemical and pharmaceutical applications.

Check Digit Verification of cas no

The CAS Registry Mumber 464-15-3 includes 6 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 3 digits, 4,6 and 4 respectively; the second part has 2 digits, 1 and 5 respectively.
Calculate Digit Verification of CAS Registry Number 464-15:
(5*4)+(4*6)+(3*4)+(2*1)+(1*5)=63
63 % 10 = 3
So 464-15-3 is a valid CAS Registry Number.
InChI:InChI=1/C10H18/c1-9(2)8-4-6-10(9,3)7-5-8/h8H,4-7H2,1-3H3

464-15-3SDS

SAFETY DATA SHEETS

According to Globally Harmonized System of Classification and Labelling of Chemicals (GHS) - Sixth revised edition

Version: 1.0

Creation Date: Aug 17, 2017

Revision Date: Aug 17, 2017

1.Identification

1.1 GHS Product identifier

Product name bornane

1.2 Other means of identification

Product number -
Other names Bicyclo[2.2.1]heptane, 1,7,7-trimethyl-

1.3 Recommended use of the chemical and restrictions on use

Identified uses For industry use only.
Uses advised against no data available

1.4 Supplier's details

1.5 Emergency phone number

Emergency phone number -
Service hours Monday to Friday, 9am-5pm (Standard time zone: UTC/GMT +8 hours).

More Details:464-15-3 SDS

464-15-3Relevant academic research and scientific papers

EPIMERIZATION OF ENDO- AND EXO-BORNEOLS IN THE PRESENCE OF AMMONIA AND/OR HYDROGEN ON A FUSED IRON CATALYST

Glebov, L. S.,Shuikin, A. N.,Kliger, G. A.,Loktev, S. M.

, p. 1985 - 1987 (2007/10/02)

Epimerization of borneols was noted upon their reaction with ammonia and/or hydrogen on fused iron catalyst.Borneols are hydroaminated to give bornylamines with predominance of the endo isomer.

Heterogeneous Catalysis, VI. Direct Reduction of Alcohols to Hydrocarbons

Maier, Wilhelm F.,Thies, Irina,Rague Schleyer, Paul von

, p. 392 - 394 (2007/10/02)

Secondary and tertiary alcohols are converted cleanly to the parent hydrocarbons in the gas phase with H2 in the presence of a Ni/Al2O3 catalyst at 190 deg C.Primary alcohols are dehydroxymethylated; e.g., 1-hydroxymethyladamantane (4) gives adamantane (1).Alumina alone, in the absence of Ni, results in the formation of homoadamantane (5) from 4. - Keywords: Gas Phase Hydrogenolysis, Homoadamantane Preparation

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