90472-95-0 Usage
Uses
Used in Pharmaceutical Synthesis:
(S)-4,5-ISOPROPYLIDENE HEXANONITRILE is used as an intermediate in the synthesis of various pharmaceuticals. Its unique structure and reactivity allow for the creation of a wide range of medicinal compounds, contributing to the development of new drugs and therapies.
Used in Agrochemical Production:
In the agrochemical industry, (S)-4,5-ISOPROPYLIDENE HEXANONITRILE serves as an essential intermediate for the production of various agrochemicals. Its role in the synthesis of these compounds aids in the development of effective pesticides, herbicides, and other agricultural products.
Used in Organic Synthesis:
(S)-4,5-ISOPROPYLIDENE HEXANONITRILE is utilized as a building block in organic synthesis, enabling the creation of more complex molecules for a variety of applications. Its versatility in chemical reactions makes it a valuable component in the development of new materials and compounds.
Safety Precautions:
It is crucial to handle (S)-4,5-ISOPROPYLIDENE HEXANONITRILE with care due to its potential hazards, including flammability and toxicity. Proper safety measures should be taken to minimize risks and ensure the safe use of (S)-4,5-ISOPROPYLIDENE HEXANONITRILE in various applications.
Check Digit Verification of cas no
The CAS Registry Mumber 90472-95-0 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 9,0,4,7 and 2 respectively; the second part has 2 digits, 9 and 5 respectively.
Calculate Digit Verification of CAS Registry Number 90472-95:
(7*9)+(6*0)+(5*4)+(4*7)+(3*2)+(2*9)+(1*5)=140
140 % 10 = 0
So 90472-95-0 is a valid CAS Registry Number.
InChI:InChI=1/C9H15NO2/c1-9(2)11-7-8(12-9)5-3-4-6-10/h8H,3-5,7H2,1-2H3/t8-/m0/s1
90472-95-0Relevant academic research and scientific papers
SYNTHESE ENANTIOSPECIFIQUE DU 5-HEXADECANOLIDE, PHEROMONE DE "VESPA ORIENTALIS"
Larcheveque, Marc,Lalande, Julien
, p. 1061 - 1066 (2007/10/02)
A synthetic scheme was elaborated to prepare (R)(+) δ-n-hexadecanolactone 10 in 8 steps from (L)-glutamic acid.
