19898-58-9 Usage
General Description
The chemical "(1alpha,3beta,4alpha,6alpha)-3,7,7-trimethylbicyclo[4.1.0]heptane-3,4-diol" is a bicyclic compound with a molecular formula of C10H18O2. It is also known as isopinocampheol and is a naturally occurring compound found in certain plants and essential oils. It is classified as a bicyclic alcohol due to its structure, and it has been studied for its potential pharmaceutical and medicinal properties. (1alpha,3beta,4alpha,6alpha)-3,7,7-trimethylbicyclo[4.1.0]heptane-3,4-diol has been shown to have antimicrobial and anti-inflammatory effects, and it is used in some traditional medicine practices. Additionally, it may have potential applications in the development of new drugs or pharmaceutical products.
Check Digit Verification of cas no
The CAS Registry Mumber 19898-58-9 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 1,9,8,9 and 8 respectively; the second part has 2 digits, 5 and 8 respectively.
Calculate Digit Verification of CAS Registry Number 19898-58:
(7*1)+(6*9)+(5*8)+(4*9)+(3*8)+(2*5)+(1*8)=179
179 % 10 = 9
So 19898-58-9 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/t6-,7+,8-,10-/m1/s1
19898-58-9Relevant articles and documents
Monoterpenediol insect repellents
-
, (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.
ALKALI-CATALYZED HYDRATION OF STEREOISOMERIC 3,4-EPOXYCARANES
Kazakova, E. Kh.,Surkova, L. N.
, p. 2155 - 2156 (2007/10/02)
-
