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2,2'-Biborneol is a naturally occurring organic compound that belongs to the class of sesquiterpenes, which are derived from the isoprene unit. It is characterized by a bicyclic structure, with two borneol units connected at their 2,2' positions. 2,2'-Biborneol is found in various essential oils, particularly in the oils of plants from the Lauraceae family, such as camphor trees. 2,2'-Biborneol is known for its unique aroma and has been used in perfumery and as a flavoring agent. It is also of interest in the field of organic chemistry due to its potential applications in the synthesis of more complex molecules and its role as a chiral building block. The compound's properties, such as its optical activity and reactivity, make it a subject of study for chemists looking to understand and manipulate the behavior of sesquiterpenes in various chemical processes.

5649-82-1

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5649-82-1 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 5649-82-1 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 5,6,4 and 9 respectively; the second part has 2 digits, 8 and 2 respectively.
Calculate Digit Verification of CAS Registry Number 5649-82:
(6*5)+(5*6)+(4*4)+(3*9)+(2*8)+(1*2)=121
121 % 10 = 1
So 5649-82-1 is a valid CAS Registry Number.

5649-82-1SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 18, 2017

Revision Date: Aug 18, 2017

1.Identification

1.1 GHS Product identifier

Product name 3-(3-hydroxy-4,7,7-trimethyl-3-bicyclo[2.2.1]heptanyl)-4,7,7-trimethylbicyclo[2.2.1]heptan-3-ol

1.2 Other means of identification

Product number -
Other names 2,2'-Biborneol

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:5649-82-1 SDS

5649-82-1Downstream Products

5649-82-1Relevant academic research and scientific papers

ENANTIOSELECTIVITY IN CAMPHOR PINACOLISATION

Pradhan, Suresh K.,Thakker, Krishanlal R.,McPhail, Andrew T.

, p. 1813 - 1816 (2007/10/02)

Total enantioselectivity has been observed in pinacol formation using Li/THF. (+) Camphor and (+/-) Camphor give the optically active and racemic form of a single pinacol whose stereochemistry has been established as endo:endo by X-ray analysis.An exo:endo pinacol is formed as the sole product if camphor is added to Li/NH3.Tentative mechanism is proposed.

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