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92015-51-5

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92015-51-5 Usage

Chemical structure

Bicyclic organic compound

Usage

Synthesis of pharmaceuticals and agrochemicals

Physical state

White solid at room temperature

Solubility

Insoluble in water, soluble in organic solvents

Functional group

Carboxylic acid derivative

Application

Building block for synthesis of biologically active compounds

Molecular structure

Unique molecular structure

Additional studies

Potential applications in materials science and chemical engineering

Importance

Crucial role in the synthesis of important chemical compounds and potential applications in various fields

Check Digit Verification of cas no

The CAS Registry Mumber 92015-51-5 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 9,2,0,1 and 5 respectively; the second part has 2 digits, 5 and 1 respectively.
Calculate Digit Verification of CAS Registry Number 92015-51:
(7*9)+(6*2)+(5*0)+(4*1)+(3*5)+(2*5)+(1*1)=105
105 % 10 = 5
So 92015-51-5 is a valid CAS Registry Number.

92015-51-5SDS

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 4,5,5-trimethylbicyclo[2.1.1]hexane-6-carboxylic acid

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

1.5 Emergency phone number

Emergency phone number -
Service hours Monday to Friday, 9am-5pm (Standard time zone: UTC/GMT +8 hours).

More Details:92015-51-5 SDS

92015-51-5Downstream Products

92015-51-5Relevant articles and documents

Microwave specific Wolff rearrangement of α-diazoketones and its relevance to the nonthermal and thermal effect

Sudrik, Surendra G.,Chavan, Sambhaji P.,Chandrakumar,Pal, Sourav,Date, Sadgopal K.,Chavan, Subhash P.,Sonawane, Harikisan R.

, p. 1574 - 1579 (2007/10/03)

α-Diazoketones possess high electric dipole moments, as a consequence of the dipolar nature of the diazocarbonyl functional group. The vectorial analysis, theoretical calculations (PM3 and ab initio), and literature reports based on experimental and theor

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