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33404-67-0

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33404-67-0 Usage

Description

[1R,4R,(+)]-2,2-Dimethyl-5-methylenebicyclo[2.2.1]heptane is a bicyclic organic compound characterized by its molecular formula of C8H12. It is a colorless liquid with a pungent odor and is distinguished by its unique structural arrangement due to its bicyclic nature. [1R,4R,(+)]-2,2-Dimethyl-5-methylenebicyclo[2.2.1]heptane is known for its applications in the synthesis of pharmaceuticals and agrochemicals, as well as its use as a chiral auxiliary in asymmetric synthesis. Furthermore, it has been studied for its potential biological and pharmacological activities.

Uses

Used in Pharmaceutical Synthesis:
[1R,4R,(+)]-2,2-Dimethyl-5-methylenebicyclo[2.2.1]heptane is used as a key intermediate in the synthesis of various pharmaceuticals. Its unique structural arrangement allows for its incorporation into complex molecular structures, contributing to the development of new and effective medications.
Used in Agrochemical Synthesis:
In the agrochemical industry, [1R,4R,(+)]-2,2-Dimethyl-5-methylenebicyclo[2.2.1]heptane is utilized as a starting material for the production of various agrochemicals. Its versatility in chemical reactions enables the creation of compounds that can be used in the development of pesticides, herbicides, and other agricultural products.
Used as a Chiral Auxiliary in Asymmetric Synthesis:
[1R,4R,(+)]-2,2-Dimethyl-5-methylenebicyclo[2.2.1]heptane is employed as a chiral auxiliary in asymmetric synthesis, a crucial technique in the production of enantiomerically pure compounds. Its bicyclic structure provides a stable and easily modifiable platform for the creation of chiral molecules, which are essential in the pharmaceutical and chemical industries.
Used in Chemical Research:
[1R,4R,(+)]-2,2-Dimethyl-5-methylenebicyclo[2.2.1]heptane is also used in chemical research to study its potential biological and pharmacological activities. Its unique structure and properties make it an interesting subject for scientists to explore, potentially leading to new discoveries and applications in various fields.

Check Digit Verification of cas no

The CAS Registry Mumber 33404-67-0 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 3,3,4,0 and 4 respectively; the second part has 2 digits, 6 and 7 respectively.
Calculate Digit Verification of CAS Registry Number 33404-67:
(7*3)+(6*3)+(5*4)+(4*0)+(3*4)+(2*6)+(1*7)=90
90 % 10 = 0
So 33404-67-0 is a valid CAS Registry Number.

33404-67-0SDS

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 β-fenchene

1.2 Other means of identification

Product number -
Other names (+)-β-Fenchen

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:33404-67-0 SDS

33404-67-0Relevant articles and documents

SYNTHESIS AND STRUCTURE OF AMINO ESTERS OF FENCHOL. II.

Raikova, T. S.,Voitekhovskaya, G. I.,Vyalimyae, T. K.,Udarov, B. G.

, p. 289 - 291 (2007/10/02)

Amino derivatives of fenchol have been synthesized.Their structures and properties have been studied by physicochemical methods.

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