83406-42-2 Usage
Explanation
The compound's full name, indicating its structure and properties.
Explanation
The compound belongs to a group of chemical compounds derived from naphthalene.
3. Hexahydro derivative
Explanation
The compound has six hydrogen atoms added to its structure, making it a hexahydro derivative of naphthalenedione.
Explanation
The compound's molecular structure consists of a six-membered ring that is fused to a two-ring system, creating a complex structure.
5. Trans conformation
Explanation
The compound has a trans configuration, meaning that its functional groups are on opposite sides of the molecular plane.
Explanation
The compound is primarily used in the fields of organic synthesis and pharmaceutical research due to its unique structure and properties.
7. Potential use in pharmaceutical drugs
Explanation
The compound has potential applications in the development of pharmaceutical drugs, possibly due to its unique structure and properties.
8. Intermediate in manufacturing
Explanation
The compound can be used as an intermediate in the manufacturing of various organic compounds, making it valuable in the chemical industry.
9. Stereochemistry and reaction mechanisms
Explanation
The compound's trans configuration makes it valuable for studying stereochemistry and reaction mechanisms in organic chemistry, as it provides insights into the spatial arrangement of atoms and the pathways of chemical reactions.
Class
Naphthalene derivatives
Molecular structure
Six-membered ring fused to a two-ring system
Applications
Organic synthesis and pharmaceutical research
Check Digit Verification of cas no
The CAS Registry Mumber 83406-42-2 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 8,3,4,0 and 6 respectively; the second part has 2 digits, 4 and 2 respectively.
Calculate Digit Verification of CAS Registry Number 83406-42:
(7*8)+(6*3)+(5*4)+(4*0)+(3*6)+(2*4)+(1*2)=122
122 % 10 = 2
So 83406-42-2 is a valid CAS Registry Number.
83406-42-2Relevant articles and documents
Preparative Bioorganic Chemistry, XVII. Reduction of a Prochiral Diketone, 9-Methyl-trans-decalin-1,8-dione, with Baker's Yeast
Mori, Kenji,Takayama, Shuichi,Yoshimura, Seiji
, p. 91 - 96 (2007/10/02)
Reduction of 9-methyl-trans-decalin-1,8-dione (1) with baker's yeast affords (8S,9R,10R)-8-hydroxy-9-methyl-trans-1-decalone (8) as the major product in 47percent yield.Its (8S,9S,10S)-isomer (9, 14percent yield) and (1S,8S)-9-methyl-trans-1,8-diol (10, 7percent yield) are obtained as minor products.Baker's yeast cannot reduce 9-methyl-cis-decalin-1,8-dione (2). Key Words: Asymmetric reduction / Baker's yeast / Yeast / Saccharomyces cerevisia / Enzymes / trans-1-Decalone derivatives / trans-1,8-Decalindione derivatives
