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464-15-3

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464-15-3 Usage

General Description

Bornane is a bicyclic organic compound that belongs to the class of hydrocarbons known as norbornanes. It is a colorless, crystalline substance with a camphor-like odor. Bornane is commonly used in the synthesis of various pharmaceuticals and as a starting material in the production of fragrances and flavors. It is also used as a chiral auxiliary in asymmetric synthesis and as a building block for the preparation of polycyclic compounds. Bornane has low solubility in water and is relatively stable under normal conditions, making it a versatile and important chemical in various industrial and research 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 articles and documents

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.

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