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Bicyclo[3.2.1]octane, 1-methyl-, also known as 1-methylbicyclo[3.2.1]octane, is a cyclic hydrocarbon compound with a molecular formula of C9H16. It features a bicyclic structure with three carbon atoms in one ring and two carbon atoms in the other, connected by a bridge of one carbon atom. The methyl group is attached to the first carbon atom in the larger ring. Bicyclo[3.2.1]octane, 1-methyl- is an example of a bridged bicyclic hydrocarbon, which can exhibit unique chemical properties and reactivity due to its strained ring system. It is used in organic synthesis and as a precursor in the production of various pharmaceuticals and chemical compounds.

3673-75-4

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3673-75-4 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 3673-75-4 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 3,6,7 and 3 respectively; the second part has 2 digits, 7 and 5 respectively.
Calculate Digit Verification of CAS Registry Number 3673-75:
(6*3)+(5*6)+(4*7)+(3*3)+(2*7)+(1*5)=104
104 % 10 = 4
So 3673-75-4 is a valid CAS Registry Number.

3673-75-4SDS

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 5-methylbicyclo[3.2.1]octane

1.2 Other means of identification

Product number -
Other names 1-Methylbicyclo<3,2,1>octan

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:3673-75-4 SDS

3673-75-4Downstream Products

3673-75-4Relevant academic research and scientific papers

Radical-mediated synthesis of bridgehead-substituted bicycloalkanes. A convenient route to the bicyclo[3.2.1]octyl system

Della,Knill

, p. 3518 - 3522 (1995)

Cyclization of the (3-methylenecyclohexyl)ethyl radical (9) to the isomeric 1-bicyclo[3.2.1]octylmethyl radical (10) occurs with an activation energy of 11.6 kcal mol-1, a barrier which compares favorably with the calculated value of 12.6 kcal

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