• Chemical Name 3-(4,7,7-trimethylbicyclo[4.1.0]hept-3-ylidene)propiononitrile
  • CAS No. 68804-02-4
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What is the 3-(4,7,7-trimethylbicyclo[4.1.0]hept-3-ylidene)propiononitrile ?

3-(4,7,7-trimethylbicyclo[4.1.0]hept-3-ylidene)propiononitrile is , while it's Molecular Formula is C13H19 N. Used in Organic Synthesis:
3-(4,7,7-trimethylbicyclo[4.1.0]hept-3-ylidene)propiononitrile is used as a building block in organic synthesis for its unique structural features and reactivity, allowing for the creation of a variety of complex organic molecules.
Used in Pharmaceutical Industry:
In the pharmaceutical industry, 3-(4,7,7-trimethylbicyclo[4.1.0]hept-3-ylidene)propiononitrile is used as a key intermediate in the synthesis of various drugs, leveraging its unique structural properties to contribute to the development of novel therapeutic agents.
Used in Agrochemical Industry:
3-(4,7,7-trimethylbicyclo[4.1.0]hept-3-ylidene)propiononitrile is utilized as a starting material in the production of agrochemicals, such as pesticides and herbicides, due to its potential to form active ingredients with specific modes of action against pests and weeds.

What is the CAS number for 3-(4,7,7-trimethylbicyclo[4.1.0]hept-3-ylidene)propiononitrile ?

The CAS number of 3-(4,7,7-trimethylbicyclo[4.1.0]hept-3-ylidene)propiononitrile is 68804-02-4.

More information of 3-(4,7,7-trimethylbicyclo[4.1.0]hept-3-ylidene)propiononitrile 68804-02-4 are:

Synonyms

Sandatrile

CAS?Number

68804-02-4

Molecular Formula

C13H19 N

Molecular Weight

189.29666

Density

0.992g/cm3

Boiling Point

286.2°C at 760 mmHg

Flash Point

132.2°C

PSA

23.79000

LogP

3.52858

What is 3-(4,7,7-trimethylbicyclo[4.1.0]hept-3-ylidene)propiononitrile (68804-02-4) used for?

3-(4,7,7-trimethylbicyclo[4.1.0]hept-3-ylidene)propiononitrile is a complex nitrile compound characterized by a bicyclic structure, specifically a bicyclo[4.1.0]heptane ring system, with a propiononitrile group attached to a three-carbon chain. 3-(4,7,7-trimethylbicyclo[4.1.0]hept-3-ylidene)propiononitrile features a trimethyl substitution, where three methyl groups are attached to different carbon atoms within the bicyclic ring system. Its unique structure and reactivity make it a valuable component in organic synthesis and as a precursor for the development of pharmaceuticals and agrochemicals.

InChI:InChI=1/C13H19N/c1-9-7-11-12(13(11,2)3)8-10(9)5-4-6-14/h5,9,11-12H,4,7-8H2,1-3H3

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