94006-07-2 Usage
Description
(-)-3,4,5,6,7,8-hexahydro-1-[(4-hydroxyphenyl)methyl](1H)-isoquinoline-2-carbaldehyde is a complex chemical compound that features a cyclic isoquinoline ring and a benzene ring. It is recognized for its potential therapeutic properties and is commonly utilized in organic synthesis and pharmaceutical research.
Uses
Used in Pharmaceutical Research:
(-)-3,4,5,6,7,8-hexahydro-1-[(4-hydroxyphenyl)methyl](1H)-isoquinoline-2-carbaldehyde is used as a research compound for its potential therapeutic properties. It is being studied for its ability to inhibit certain enzymes and receptors, which may contribute to the treatment of various diseases.
Used in Organic Synthesis:
In the field of organic synthesis, (-)-3,4,5,6,7,8-hexahydro-1-[(4-hydroxyphenyl)methyl](1H)-isoquinoline-2-carbaldehyde is used as a key intermediate or building block in the creation of more complex molecules, potentially leading to the development of new pharmaceuticals or other organic compounds.
Used in Drug Development:
The unique structure and properties of (-)-3,4,5,6,7,8-hexahydro-1-[(4-hydroxyphenyl)methyl](1H)-isoquinoline-2-carbaldehyde make it a promising candidate for drug development. It is currently under investigation for its potential use in treating various diseases, although its exact therapeutic applications are still being explored.
Check Digit Verification of cas no
The CAS Registry Mumber 94006-07-2 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 9,4,0,0 and 6 respectively; the second part has 2 digits, 0 and 7 respectively.
Calculate Digit Verification of CAS Registry Number 94006-07:
(7*9)+(6*4)+(5*0)+(4*0)+(3*6)+(2*0)+(1*7)=112
112 % 10 = 2
So 94006-07-2 is a valid CAS Registry Number.
94006-07-2Relevant articles and documents
On the formation of a side product with hexahydroaporphine-like structure in the Grewe cyclization of dextromethorphan
Zhao, Qiao,Zhao, Kai,Wu, Sheng-ying,Tian, Bo-xue,Eriksson, Leif A.,Wang, Li-min,An, Na,Long, Zhong-zhu,Cai, Shui-hong
, p. 1689 - 1708 (2017/02/15)
Factors leading to the formation of a hexahydroaporphine-like cyclizing side product were studied systematically for the first time and the ratio of this side product was controlled effectively. To understand better the electronic effect of substrates on the formation of side products, different 1-benzyloctahydroisoquinolines with substituted groups on nitrogen or benzene ring were compared. A plausible mechanism of cyclizing reaction was proposed, and key intermediates as well as transition states were analyzed using DFT calculations.