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Bicyclo[2.1.1]hexane-1-carboxylic acid, 5,5-dimethyl-, also known as 5,5-dimethylbicyclo[2.1.1]hexane-1-carboxylic acid, is a chemical compound with the molecular formula C9H14O2. It is a white crystalline solid that is soluble in organic solvents. Bicyclo[2.1.1]hexane-1-carboxylic acid, 5,5-dimethyl- is a derivative of bicyclo[2.1.1]hexane, a bicyclic hydrocarbon, with a carboxylic acid group attached to the first carbon and two methyl groups attached to the fifth carbon. It is used as an intermediate in the synthesis of various pharmaceuticals and agrochemicals, particularly in the production of certain insecticides and antifungal agents. The compound is also known for its potential use in the development of new materials with unique properties, such as in the field of polymer chemistry.

3753-38-6

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3753-38-6 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 3753-38-6 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 3,7,5 and 3 respectively; the second part has 2 digits, 3 and 8 respectively.
Calculate Digit Verification of CAS Registry Number 3753-38:
(6*3)+(5*7)+(4*5)+(3*3)+(2*3)+(1*8)=96
96 % 10 = 6
So 3753-38-6 is a valid CAS Registry Number.

3753-38-6SDS

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 5,5-Dimethyl-bicyclo[2.1.1]hexan-1-carbonsaeure

1.2 Other means of identification

Product number -
Other names -

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

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More Details:3753-38-6 SDS

3753-38-6Relevant academic research and scientific papers

About the participation of σ, π and n orbitals in the solvolysis of 2- and 3-oxo-1-norbornyl triflates

Martinez, Antonio Garcia,Barcina, Jose Osio,Vilar, Enrique Teso

, p. 14041 - 14048 (1996)

The solvolysis of 3,3-dimethyl-2-oxo- and 2,2-dimethyl-3-oxo-1-norbornyltriflates (6 and 8) takes place with formation of ring contracted and fragmented products respectively. The effect of the substituents on the solvolysis rates is explained taking into account n- and σ-participation. This n,σ-participation causes changes in the structure and stability of the intermediate carbocations, which can be detected by the AM1 method.

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