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7-Azabicyclo(2.2.1)heptadiene-7-carboxylic acid, methyl ester is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

83060-75-7

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83060-75-7 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 83060-75-7 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 8,3,0,6 and 0 respectively; the second part has 2 digits, 7 and 5 respectively.
Calculate Digit Verification of CAS Registry Number 83060-75:
(7*8)+(6*3)+(5*0)+(4*6)+(3*0)+(2*7)+(1*5)=117
117 % 10 = 7
So 83060-75-7 is a valid CAS Registry Number.
InChI:InChI=1/C8H9NO2/c1-11-8(10)9-6-2-3-7(9)5-4-6/h2-7H,1H3

83060-75-7SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 14, 2017

Revision Date: Aug 14, 2017

1.Identification

1.1 GHS Product identifier

Product name Methyl 7-azabicyclo[2.2.1]hepta-2,5-diene-7-carboxylate

1.2 Other means of identification

Product number -
Other names 7-(methoxycarbonyl)-7-azabicyclo[2.2.1]hepta-2,5-diene

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:83060-75-7 SDS

83060-75-7Relevant academic research and scientific papers

Development of two processes for the synthesis of bridged azabicyclic systems: Intermolecular radical addition-homoallylic rearrangements leading to 2-azanorborn-5-enes and neophyl-type radical rearrangements to 2-azabenzonorbornanes

Hodgson, David M.,Bebbington, Magnus W.P.,Willis, Paul

, p. 3787 - 3798 (2007/10/03)

Radical thiol additions to 7-azanorbornadienes give 7-thio-substituted 2-azanorbornenes and Barton deoxygenations of 7-azabenzonorbornanols give 2-azabenzonorbornanes. The processes both involve novel nitrogen-directed radical rearrangements. The kinetics and mechanisms of the reactions are also discussed.

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