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Bicyclo[3.2.1]oct-6-ene is a bicyclic hydrocarbon compound with the molecular formula C8H12. It features a unique structure consisting of two carbon rings, with one being a cyclopropane ring and the other a cyclohexane ring, connected at a quaternary carbon atom. Bicyclo[3.2.1]oct-6-ene is known for its strained ring system, which results in high reactivity and potential applications in organic synthesis. Bicyclo[3.2.1]oct-6-ene is also an important intermediate in the synthesis of various natural products and pharmaceuticals, such as the synthesis of steroids and other complex organic molecules. Its chemical properties, including its reactivity and stability, make it a valuable compound for research and development in the field of organic chemistry.

6491-96-9

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6491-96-9 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 6491-96-9 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 6,4,9 and 1 respectively; the second part has 2 digits, 9 and 6 respectively.
Calculate Digit Verification of CAS Registry Number 6491-96:
(6*6)+(5*4)+(4*9)+(3*1)+(2*9)+(1*6)=119
119 % 10 = 9
So 6491-96-9 is a valid CAS Registry Number.

6491-96-9SDS

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 bicyclo[3.2.1]oct-6-ene

1.2 Other means of identification

Product number -
Other names Bicyclo<3.2.1>oct-6-en

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

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More Details:6491-96-9 SDS

6491-96-9Downstream Products

6491-96-9Relevant academic research and scientific papers

BRIDGING STRAIN IN BICYCLIC CARBOCATIONS

Grob, Cyril A,Zutter, Ulrich

, p. 2849 - 2852 (1982)

The solvolysis rates and products of 6-exo- and 6-endo-bicyclooctyl toluenesulfonate confirm that differential bridging strain is a major factor in determining the reactivity of epimeric bicyclic sulfonates.

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