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Bicyclo[2.2.1]heptan-2-one, 3-hydroxy-, exo-, also known as Norcamphor or exo-3-Hydroxybicyclo[2.2.1]heptan-2-one, is a naturally occurring organic compound with the molecular formula C7H10O2. It is a bicyclic ketone with a hydroxyl group attached to the third carbon atom in the exo position, which means it is located on the outside of the ring. Bicyclo[2.2.1]heptan-2-one, 3-hydroxy-, exo- is an important intermediate in the synthesis of various natural products and pharmaceuticals, such as camphor and other terpenoids. Norcamphor is known for its unique structure and properties, including its ability to undergo various chemical reactions, such as oxidation, reduction, and rearrangement. It is also used as a chiral auxiliary in asymmetric synthesis and as a building block in the preparation of complex organic molecules.

5164-67-0

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5164-67-0 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 5164-67-0 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 5,1,6 and 4 respectively; the second part has 2 digits, 6 and 7 respectively.
Calculate Digit Verification of CAS Registry Number 5164-67:
(6*5)+(5*1)+(4*6)+(3*4)+(2*6)+(1*7)=90
90 % 10 = 0
So 5164-67-0 is a valid CAS Registry Number.

5164-67-0SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 15, 2017

Revision Date: Aug 15, 2017

1.Identification

1.1 GHS Product identifier

Product name exo-3-hydroxy-bicyclo(2.2.1)heptan-2-one

1.2 Other means of identification

Product number -
Other names 2-exo-hydroxynorbornan-3-one

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:5164-67-0 SDS

5164-67-0Upstream product

5164-67-0Relevant academic research and scientific papers

Protonated cyclopropanes in α-aminoketone deamination

Edwards, Oliver E.,Dixon, John,Elder, John W.,Kolt, Ralph J.,Lesage, Maurice

, p. 2096 - 2115 (2007/10/02)

Deamination of 2-amino-4,4-dideuterio-6,6-dimethylcyclohexanone, 2-exo-amino- and 2-endo-amino-norbornane-3-one, 2-diazo-norbornan-3-one, 2-exo-amino-5,6-exo-dideuterionorbornan-3-one and the corresponding 5,6-endo-dideuterio isomer has been studied.The nature of the products, the deuterium location in them, and the high retention of steric identity in the carbocations are interpreted in terms of ?-bond participation leading to corner- and edge-protonated cyclopropanes as reaction intermediates.Results with other destabilized carbocations are correlated.

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