55812-82-3 Usage
Description
7a-Methyl-1-(1,4,5-trimethyl-hex-2-enyl)-octahydro-inden-4-ol is a complex organic compound with a unique molecular structure. It is a colorless oil, which indicates its liquid state at room temperature and its lack of color. 7a-Methyl-1-(1,4,5-trimethyl-hex-2-enyl)-octahydro-inden-4-ol is synthesized as a byproduct during the preparation of Vitamin D derivatives, suggesting its potential use in the pharmaceutical industry.
Uses
Used in Pharmaceutical Industry:
7a-Methyl-1-(1,4,5-trimethyl-hex-2-enyl)-octahydro-inden-4-ol is used as an intermediate in the synthesis of Vitamin D derivatives for the pharmaceutical industry. Its role in the production process is crucial, as it contributes to the development of essential vitamins that play a vital role in maintaining human health.
Used in Chemical Research:
As a complex organic compound, 7a-Methyl-1-(1,4,5-trimethyl-hex-2-enyl)-octahydro-inden-4-ol can also be used as a subject of study in chemical research. Its unique structure and properties may provide insights into the development of new compounds or the understanding of specific chemical reactions and mechanisms.
Used in the Synthesis of Other Compounds:
Due to its complex structure, 7a-Methyl-1-(1,4,5-trimethyl-hex-2-enyl)-octahydro-inden-4-ol may serve as a starting material or a building block in the synthesis of other organic compounds. Its versatility in chemical reactions can be exploited to create new molecules with potential applications in various industries, such as pharmaceuticals, materials science, or agrochemicals.
Check Digit Verification of cas no
The CAS Registry Mumber 55812-82-3 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 5,5,8,1 and 2 respectively; the second part has 2 digits, 8 and 2 respectively.
Calculate Digit Verification of CAS Registry Number 55812-82:
(7*5)+(6*5)+(5*8)+(4*1)+(3*2)+(2*8)+(1*2)=133
133 % 10 = 3
So 55812-82-3 is a valid CAS Registry Number.
InChI:InChI=1/C19H34O/c1-13(2)14(3)8-9-15(4)16-10-11-17-18(20)7-6-12-19(16,17)5/h8-9,13-18,20H,6-7,10-12H2,1-5H3/b9-8+/t14-,15+,16+,17?,18-,19+/m0/s1
55812-82-3Relevant articles and documents
Probing the structural requirements for vitamin D3 inhibition of the hedgehog signaling pathway
Deberardinis, Albert M.,Banerjee, Upasana,Miller, Michele,Lemieux, Steven,Hadden
scheme or table, p. 4859 - 4863 (2012/08/13)
A structure-activity relationship study to elucidate the structural basis for hedgehog (Hh) signaling inhibition by vitamin D3 (VD3) was performed. Functional and non-functional regions of VD3 and VD2 were obtained through straightforward synthetic means
Preparation of an A-ring building block for the total synthesis of 1α,25-dihydroxy vitamin D3 and structurally related congeners: Lipase-catalyzed stereoselective esterification of a suitable epoxyalcohol
Ferraboschi, Patrizia,Reza-Elahi, Shahrzad,Scotti, Luca,Santaniello, Enzo
, p. 2665 - 2668 (2007/10/03)
An useful A-ring building block for the total synthesis of vitamin D3 congeners, compound 7, has been prepared starting from vitamin D2 by a chemo-enzymatic approach that relies on lipase-catalyzed acylation in an organic solvent for the stereoselective step. Copyright (C) 2000 Elsevier Science Ltd.
On the Julia Alkenylation reaction in vitamin D synthesis. Isolation of four geometrical isomers of vitamin D4
Blakmore,Grzywacz,Kocienski,Marczak,Wicha
, p. 1209 - 1217 (2007/10/03)
Coupling of sulfone 2 and aldehyde 3b using the Julia alkenylation procedure has been reexamined using modern product separation techniques. It was found that vitamin D4 1b and its geometric isomers 10, 11 and 12 are formed in a ratio of 75:10:10:5, respectively. The building blocks 2 and 3b were prepared from vitamin D2. Correlations for the structure assignment of vitamin D stereoisomers by 1H NMR spectroscopy are presented.