29804-22-6 Usage
Description
(+/-)-CIS-7,8-EPOXY-2-METHYLOCTADECANE is a complex organic compound with a unique molecular structure, characterized by the presence of an epoxy group at the 7,8 positions and a methyl group at the 2nd carbon atom in an octadecane chain. (+/-)-CIS-7,8-EPOXY-2-METHYLOCTADECANE exhibits specific chemical properties and reactivity, making it a versatile molecule with potential applications in various industries.
Uses
Used in Chemical Synthesis:
(+/-)-CIS-7,8-EPOXY-2-METHYLOCTADECANE is used as a key intermediate in the synthesis of various specialty chemicals, including pharmaceuticals, agrochemicals, and fragrances. Its unique structural features allow for selective functionalization and modification, enabling the development of novel compounds with specific biological activities or improved properties.
Used in Pharmaceutical Industry:
(+/-)-CIS-7,8-EPOXY-2-METHYLOCTADECANE is used as a building block for the development of new drugs, particularly those targeting specific biological pathways or receptors. Its structural diversity and reactivity make it a valuable candidate for the design of innovative therapeutic agents with improved efficacy and selectivity.
Used in Agrochemical Industry:
(+/-)-CIS-7,8-EPOXY-2-METHYLOCTADECANE is used as a component in the formulation of pheromone-based insect control agents, such as disparlure and monachalure, for the management of Lymantria insect pests in forest tree cultures. Its incorporation into these pheromone preparations helps to effectively control and reduce the population of these pests, thereby protecting the health and productivity of forest ecosystems.
Used in Material Science:
(+/-)-CIS-7,8-EPOXY-2-METHYLOCTADECANE can be utilized as a component in the development of advanced materials, such as polymers, coatings, and adhesives, due to its unique chemical properties and reactivity. Its incorporation into these materials can lead to improved performance characteristics, such as enhanced mechanical strength, chemical resistance, or thermal stability.
Check Digit Verification of cas no
The CAS Registry Mumber 29804-22-6 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 2,9,8,0 and 4 respectively; the second part has 2 digits, 2 and 2 respectively.
Calculate Digit Verification of CAS Registry Number 29804-22:
(7*2)+(6*9)+(5*8)+(4*0)+(3*4)+(2*2)+(1*2)=126
126 % 10 = 6
So 29804-22-6 is a valid CAS Registry Number.
InChI:InChI=1/C19H38O/c1-4-5-6-7-8-9-10-11-15-18-19(20-18)16-13-12-14-17(2)3/h17-19H,4-16H2,1-3H3/t18-,19+/m0/s1
29804-22-6Relevant articles and documents
A new stereoselective synthesis of racemic disparlure, the sex pheromone of gypsy moth (Porthetria dispar L.)
Tolstikov,Odinokov,Galeeva,Bakeeva
, p. 1857 - 1858 (1978)
-
Concise syntheses of insect pheromones using Z-Selective cross metathesis
Herbert, Myles B.,Marx, Vanessa M.,Pederson, Richard L.,Grubbs, Robert H.
, p. 310 - 314 (2013/02/23)
Very short synthetic routes to nine cisolefin-containing pheromones containing a variety of functionality, including an unconjugated (E,Z) diene, are reported (see scheme). These lepidopteran pheromones are used extensively for pest control, and were easily prepared using ruthenium-based Z-selective cross metathesis, highlighting the advantages of this method over less efficient ways to form Z olefins.
New synthesis of (±)-cis-disparlure, pheromone of female gypsy moth (Porthetria dispar) species
Kel'in,Kulinkovich
, p. 1446 - 1448 (2007/10/03)
(±)-cis-Disparlure was synthesized in an overall yield of 50% via stereoselective addition of isoheptylmagnesium bromide to α-bromododecanal.
