92464-82-9 Usage
Description
Benzene, 1,1',1''-[[(3,7-dimethyl-2,6-octadienyl)oxy]methylidyne]tris-, (E)is an organic compound that serves as an intermediate in the synthesis of Juvenile Hormone II. Juvenile Hormone II is an acyclic sesquiterpenoid that plays a crucial role in regulating various aspects of insect physiology, including development, reproduction, diapause, and polyphenisms.
Uses
Used in Insect Physiology Research:
Benzene, 1,1',1''-[[(3,7-dimethyl-2,6-octadienyl)oxy]methylidyne]tris-, (E)is used as an intermediate in the synthesis of Juvenile Hormone II for insect physiology research. This hormone is essential in regulating various aspects of insect development, reproduction, diapause, and polyphenisms, making it a valuable tool for studying insect behavior and physiology.
Used in Pest Control:
Benzene, 1,1',1''-[[(3,7-dimethyl-2,6-octadienyl)oxy]methylidyne]tris-, (E)can be used as a component in the development of pest control strategies. By understanding the role of Juvenile Hormone II in insect physiology, researchers can develop targeted approaches to control pest populations, potentially reducing the need for harmful chemical pesticides.
Used in Pharmaceutical Industry:
Benzene, 1,1',1''-[[(3,7-dimethyl-2,6-octadienyl)oxy]methylidyne]tris-, (E)may also have potential applications in the pharmaceutical industry. Benzene, 1,1',1''-[[(3,7-dimethyl-2,6-octadienyl)oxy]methylidyne]tris-,
(E)-'s role in the synthesis of Juvenile Hormone II could lead to the development of new drugs or therapies that target insect-related diseases or conditions, offering novel treatment options for various medical applications.
Check Digit Verification of cas no
The CAS Registry Mumber 92464-82-9 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 9,2,4,6 and 4 respectively; the second part has 2 digits, 8 and 2 respectively.
Calculate Digit Verification of CAS Registry Number 92464-82:
(7*9)+(6*2)+(5*4)+(4*6)+(3*4)+(2*8)+(1*2)=149
149 % 10 = 9
So 92464-82-9 is a valid CAS Registry Number.
92464-82-9Relevant articles and documents
Indium-mediated cleavage of the trityl group from protected alcohols and diols
Behloul, Cherif,Chouti, Aicha,Guijarro, David,Foubelo, Francisco,Nájera, Carmen,Yus, Miguel
, p. 7937 - 7941 (2016/11/19)
The reaction of primary, secondary, allylic and benzylic trityl ethers with indium powder in MeOH/NH4Cl led to reductive cleavage of the trityl-oxygen bond, affording the corresponding alcohols in good to excellent yield under very mild reaction conditions. The detritylation process could successfully be extended to mono and detritylated diols. This methodology represents a new and efficient detritylation procedure under mild reaction conditions.
THE PHOTOCHEMISTRY OF METHYL GERANATE, A MODEL CHROMOPHORE FOR INSECT JUVENILE HORMONE ANALOGS
Freeman, Peter K.,Siggel, Lorenz,Chamberlain, Paul H.,Clapp, Gary E.
, p. 5051 - 5064 (2007/10/02)
The irradiation of methyl geranate (3) in ether using 254 nm lamps produces methyl 5-methyl-2-isopropenyl-4-hexenoate (13), 1,6,6-trimethyl-endo-5-carbomethoxybicyclo-hexane (11), methyl 2-isopropenyl-5-methylcyclopentanecarboxylate (12) and methyl (3Z)-3,7-dimethyl-3,6-octadienoate (14).Photolysis run in water or in ether in the presence of base generates two additional dienes: methyl 3-methylene-7-methyl-6-octaenoate (16) and methyl (3E)-3,7-dimethyl-3,6-octadienoate (17).The photolysis of methyl (2E, 6E)-3,7-dimethyl-2,6-nonadienoate (4a) in ether procedures all Z/E isomers, 4a - 4d.
