74635-87-3 Usage
Uses
Given the provided materials, there are no specific applications listed for (4S,4aR,8aS)-4-(Hydroxymethyl)-3,4a,8,8-tetramethyl-4a,5,6,7,8,8a-hexahydronaphthalen-1(4H)-one. However, considering its structural complexity and the presence of a hydroxymethyl group, it could potentially be used in various applications such as pharmaceuticals, materials science, or chemical synthesis, pending further investigation into its properties and potential reactivity.
If future research were to identify specific uses, the applications could be listed as follows:
Used in Pharmaceutical Industry:
(4S,4aR,8aS)-4-(Hydroxymethyl)-3,4a,8,8-tetramethyl-4a,5,6,7,8,8a-hexahydronaphthalen-1(4H)-one could be used as a [specific application type] for [reason for application, e.g., targeting a particular biological pathway or serving as a key intermediate in drug synthesis].
Used in Materials Science:
In the field of materials science, (4S,4aR,8aS)-4-(Hydroxymethyl)-3,4a,8,8-tetramethyl-4a,5,6,7,8,8a-hexahydronaphthalen-1(4H)-one might be used as a [specific application type] for [reason for application, e.g., enhancing the properties of a polymer or creating a new class of materials with unique characteristics].
Check Digit Verification of cas no
The CAS Registry Mumber 74635-87-3 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 7,4,6,3 and 5 respectively; the second part has 2 digits, 8 and 7 respectively.
Calculate Digit Verification of CAS Registry Number 74635-87:
(7*7)+(6*4)+(5*6)+(4*3)+(3*5)+(2*8)+(1*7)=153
153 % 10 = 3
So 74635-87-3 is a valid CAS Registry Number.
74635-87-3Relevant academic research and scientific papers
Synthesis of drimanes from (+)-larixol
Lagnel,Morin,De Groot
, p. 1907 - 1916 (2007/10/03)
The selective transformation of the side chain of larixol 1 to a functionalized one-carbon moiety leads to 6,8-diacetoxydrimenal 13, which was converted to the drimanes (-)-albrassitriol (2), (-)-drimenol (3), (-)-uvidin C (4) and (-)-epi-albrassitriol (5).
SYNTHETIC STUDIES ON BIOLOGICALLY ACTIVE NATURAL COMPOUNDS. PART I: STEREOSPECIFIC TRANSFORMATION OF UVIDIN A INTO (-)-CINNAMODIAL
Garlaschelli, L.,Vidari, G.
, p. 7371 - 7378 (2007/10/02)
A partial synthesis of (-)-cinnamodial (1) has been achived, using (+)-uvidin A (3) as starting material.This also represents a formal synthesis of (-)-cinnamosmolide (2a) and pereniporin B (2b).
Fungal Metabolites. Part 5. Uvidins, New Drimane Sesquiterpenes from Lactarius uvidus Fries
Bernardi, Maria De,Mellerio, Giorgio,Vidari, Giovanni,Vita-Finzi, Paola,Fronza, Giovanni
, p. 221 - 226 (2007/10/02)
Uvidin A (IIa) and uvidin B (IIc) along with (-)-drimenol have been isolated from Lactarius uvidus Fries (Basidiomycetes).The structure and the stereochemistry of the two uvidins have been determined both by spectroscopic data and chemical reactions.Compound (IIa) has been correlated with (+)-drimanol (VIII) by transformations into (VI) and then (VII).Reactions and spectroscopic data are discussed.
