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1,2,2,3-tetramethylbicyclo[1.1.0]butane is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

32348-64-4

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32348-64-4 Usage

Abbreviation

TMBB

Type of compound

Bicyclic hydrocarbon

Structure

Three-membered ring fused to a four-membered ring

Strain

Highly strained molecule

Reactivity

Reactive and unstable due to high strain

Applications

Model compound for studying reactivity and stability of strained molecules, potential use in materials science, and as a building block for synthesis of novel organic molecules

Significance

Valuable for understanding behavior of strained hydrocarbons and exploring new areas of chemical research

Check Digit Verification of cas no

The CAS Registry Mumber 32348-64-4 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 3,2,3,4 and 8 respectively; the second part has 2 digits, 6 and 4 respectively.
Calculate Digit Verification of CAS Registry Number 32348-64:
(7*3)+(6*2)+(5*3)+(4*4)+(3*8)+(2*6)+(1*4)=104
104 % 10 = 4
So 32348-64-4 is a valid CAS Registry Number.

32348-64-4SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 17, 2017

Revision Date: Aug 17, 2017

1.Identification

1.1 GHS Product identifier

Product name 1,2,2,3-tetramethylbicyclo[1.1.0]butane

1.2 Other means of identification

Product number -
Other names 1,2,2,3-tetramethylbicyclobutane

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:32348-64-4 SDS

32348-64-4Relevant academic research and scientific papers

REACTIONS OF CARBENES WITH BICYCLOBUTANES. III. REGIOSELECTIVITY OF THE REACTION OF DICHLOROCARBENE WITH UNSYMMETRICALLY SUBSTITUTED BICYCLOBUTANES

Koptelov, Yu. V.,Kostikov, R. R.,Molchanov, A. P.

, p. 1675 - 1679 (2007/10/02)

Dichlorocarbene reacts with laterally-substituted bicyclobutanes to give exclusively 1,4-pentadienes.With unsymmetrically bridgehead-substituted alkylbicyclobutanes, attack of the carbene is regioselective at the unsubstituted nodal atom, followed by clea

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