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Bicyclo[2.2.1]heptan-7-one, 2-hydroxy-, (1S,2R,4R)- is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

97858-70-3

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97858-70-3 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 97858-70-3 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 9,7,8,5 and 8 respectively; the second part has 2 digits, 7 and 0 respectively.
Calculate Digit Verification of CAS Registry Number 97858-70:
(7*9)+(6*7)+(5*8)+(4*5)+(3*8)+(2*7)+(1*0)=203
203 % 10 = 3
So 97858-70-3 is a valid CAS Registry Number.

97858-70-3SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 20, 2017

Revision Date: Aug 20, 2017

1.Identification

1.1 GHS Product identifier

Product name (+)-(1S,2R,4R)-2-exo-hydroxynorbornan-7-one

1.2 Other means of identification

Product number -
Other names (1S,2R,4R)-2-Hydroxy-bicyclo[2.2.1]heptan-7-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:97858-70-3 SDS

97858-70-3Relevant 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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