10395-46-7 Usage
Description
[1S-(1alpha,3alpha,4beta,6alpha)]-3,7,7-trimethylbicyclo[4.1.0]heptane-3,4-diol is a bicyclic compound characterized by two fused cyclohexane rings. It has a molecular formula of C10H18O2 and a molecular weight of 170.25 g/mol. As a diol, it features two hydroxyl (OH) functional groups. The stereochemistry of the molecule is defined by the 1S-(1alpha,3alpha,4beta,6alpha) prefix, which specifies the configuration of its four stereocenters. This unique structure and properties may offer potential applications in organic and medicinal chemistry.
Uses
Used in Organic Chemistry:
[1S-(1alpha,3alpha,4beta,6alpha)]-3,7,7-trimethylbicyclo[4.1.0]heptane-3,4-diol is used as a building block for the synthesis of more complex organic molecules due to its unique bicyclic structure and diol functional groups.
Used in Medicinal Chemistry:
In the field of medicinal chemistry, [1S-(1alpha,3alpha,4beta,6alpha)]-3,7,7-trimethylbicyclo[4.1.0]heptane-3,4-diol is used as a starting material for the development of novel pharmaceutical compounds. Its specific stereochemistry and functional groups can be exploited to create molecules with potential therapeutic applications.
Used in Pharmaceutical Industry:
Within the pharmaceutical industry, [1S-(1alpha,3alpha,4beta,6alpha)]-3,7,7-trimethylbicyclo[4.1.0]heptane-3,4-diol is used as an intermediate in the production of various drugs. Its unique structural features make it a valuable component in the design and synthesis of new medications.
Used in Chemical Research:
[1S-(1alpha,3alpha,4beta,6alpha)]-3,7,7-trimethylbicyclo[4.1.0]heptane-3,4-diol is also used as a research tool in chemical laboratories. Its distinct stereochemistry and functional groups make it an interesting subject for studying reaction mechanisms, stereoselectivity, and the development of new synthetic methods.
Check Digit Verification of cas no
The CAS Registry Mumber 10395-46-7 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 1,0,3,9 and 5 respectively; the second part has 2 digits, 4 and 6 respectively.
Calculate Digit Verification of CAS Registry Number 10395-46:
(7*1)+(6*0)+(5*3)+(4*9)+(3*5)+(2*4)+(1*6)=87
87 % 10 = 7
So 10395-46-7 is a valid CAS Registry Number.
InChI:InChI=1/C10H18O2/c1-9(2)6-4-8(11)10(3,12)5-7(6)9/h6-8,11-12H,4-5H2,1-3H3
10395-46-7Relevant articles and documents
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Kropp,P.J.
, p. 4926 - 4934 (1966)
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MECHANISM OF REARRANGEMENT WITH CYCLOPROPYL INVOLVEMENT IN ACETYLOSIS OF β-3,4-EPOXYCARANE
Arbuzov, B. A.,Isaeva, Z. G.,D'yakonova, R. R.
, p. 1949 - 1951 (1980)
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Monoterpenediol insect repellents
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, (2008/06/13)
An insect repellent comprising as an active ingredient a monoterpenediol compound having the formula, STR1 wherein R1, R2 and R3 have either one of the following definitions: (i) all of R1, R2 and R3 are hydrogen, (ii) R1 is hydrogen and R2 and R3, taken together, form a carbon-carbon single bond, or (iii) R2 is hydrogen, R1 and R3, taken together, form a carbon-carbon single bond, and the hydroxyl bonded to the carbon atom marked with an asterisk takes an α-configuration.
Transformations of 3-carene oxide at rhenium-containing catalysts
Manukov, E. N.,Bazhina, G. N.
, p. 106 - 110 (2007/10/02)
The transformations of 3-carene oxide at rhenium-containing catalysts were studied.The introduction of rhenium into the catalytic system significantly increases the reaction rate and leads to the formation of compounds not previously encountered in the products from the isomerization of 3-carene oxide, i.e., 3-carene, 3(10),4-caradiene, 3,3,6-trimethylcycloheptanone, and 3-caren-10-ol.
STEREOCHEMISTRY OF THE CARANE SYSTEM. OXIDATION PRODUCTS OF ISOMERIC 3,4-CARANEDIOLS OBTAINED FROM (+)-3-CARENE
Hendrich, Aleksandra,Piatkowski, Krzysztof
, p. 73 - 84 (2007/10/02)
Oxidation of four isomeric 3,4-caranediols has been carried out and reaction products have been investigated.It has been found that cis-diols rather form cyclic ketals than are oxidized under conditions of the Jones reaction.The key intermediate for syntheses of chrysanthemic acid, (-)-2-acetonyl-3,3-dimethylcyclopropaneacetic acid was obtained exclusively by oxidation of (-)-3β,4α-caranediol.