70120-10-4 Usage
Description
(Z)-1-(1,1-DiMethyl-2-heptenyl)-3-(phenylMethoxy)benzene is a complex organic compound with a unique molecular structure that features a di-methyl heptenyl group and a phenylmethoxy group attached to a benzene ring. (Z)-1-(1,1-DiMethyl-2-heptenyl)-3-(phenylMethoxy)benzene is characterized by its distinct chemical properties and potential applications in various fields.
Uses
Used in Pharmaceutical Industry:
(Z)-1-(1,1-DiMethyl-2-heptenyl)-3-(phenylMethoxy)benzene is used as an intermediate in the synthesis of 3-[2-Hydroxy-4-(substituted) phenyl]azacycloalkanes, which are analgesic agents. These agents are valuable for their pain-relieving properties and can be used to develop new medications for the treatment of various types of pain.
As an intermediate in the synthesis of analgesic agents, (Z)-1-(1,1-DiMethyl-2-heptenyl)-3-(phenylMethoxy)benzene plays a crucial role in the development of pharmaceuticals that can provide effective pain relief to patients. Its unique structure and properties make it a promising candidate for further research and development in the pharmaceutical industry.
Check Digit Verification of cas no
The CAS Registry Mumber 70120-10-4 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 7,0,1,2 and 0 respectively; the second part has 2 digits, 1 and 0 respectively.
Calculate Digit Verification of CAS Registry Number 70120-10:
(7*7)+(6*0)+(5*1)+(4*2)+(3*0)+(2*1)+(1*0)=64
64 % 10 = 4
So 70120-10-4 is a valid CAS Registry Number.
70120-10-4Relevant articles and documents
A Cannabinoid Derived Prototypical Analgesic
Melvin, Lawrence S.,Johnson, M. Ross,Harbert, Charles A.,Milne, George M.,Weissman, Albert
, p. 67 - 71 (2007/10/02)
The synthesis and analgesic testing of 3-cyclohexanol (1) are described.Prior (SAR) studies led us to conclude that the pyran ring of 9-nor-9β-hydroxyhexahydrocannabinol (HHC) was not necessary for the expression of biological activity in this series of cannabinoids.Analysis of models and the use of molecular mechanics calculations suggested that a simpler compound, such as 1, would possess the biological activity of HHC.Compound 1 was prepared in nine steps from acetonitrile (2).Biological testing in five models of pain shows that compound 1 and morphine are equally potent as analgesics and demonstrates that the pyran ring of HHC is not necessary for biological activity.Further simplification of 1 was pursued by the synthesis of 4--2-pentanol (17), but this derivative exhibits significantly reduced analgesic activity.
