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7787-78-2

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7787-78-2 Usage

Molecular weight

164.28 g/mol

Structure

A cyclic organic compound with a spiro ring structure, containing one oxygen atom.

Substituents

6-(1,1-dimethylethyl)group, a tert-butyl group, located on the same side of the molecule as the oxygen atom.

Conformation

The "cis-" prefix indicates that the substituents are located on the same side of the molecule.

Usage

Commonly used in the pharmaceutical and chemical industries as a building block in the synthesis of various organic compounds.

Value

Its unique structural features make it a valuable intermediate for the production of pharmaceuticals, agrochemicals, and other specialty chemicals.

Check Digit Verification of cas no

The CAS Registry Mumber 7787-78-2 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 7,7,8 and 7 respectively; the second part has 2 digits, 7 and 8 respectively.
Calculate Digit Verification of CAS Registry Number 7787-78:
(6*7)+(5*7)+(4*8)+(3*7)+(2*7)+(1*8)=152
152 % 10 = 2
So 7787-78-2 is a valid CAS Registry Number.

7787-78-2SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 12, 2017

Revision Date: Aug 12, 2017

1.Identification

1.1 GHS Product identifier

Product name 1-Methylen-4-tert-butyl-cyclohexan-epoxid, cis

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:7787-78-2 SDS

7787-78-2Relevant articles and documents

Carbodiimide-Promoted Olefin Epoxidation with Aqueous Hydrogen Peroxide

Majetich, George,Hicks, Rodgers,Sun, Guang-Ri,McGill, Patrick

, p. 2564 - 2573 (2007/10/03)

Commercially available carbodiimides in hydroxylic solvents containing hydrogen peroxide with mildly basic or acidic catalysts have been found to promote the epoxidation of olefins. A commercially available 30% aqueous solution of hydrogen peroxide serves as the oxidant for this process. The presumed reactive species is a peroxyisourea generated in situ by the addition of hydrogen peroxide to the carbodiimide.

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