19898-59-0 Usage
General Description
(1alpha,3alpha,4alpha,6alpha)-3,7,7-trimethylbicyclo[4.1.0]heptane-3,4-diol, also known as norcamphorol, is a bicyclic alcohol compound that is derived from camphor. It is a colorless, crystalline solid with a camphor-like odor. This chemical has been found to have insecticidal and antimicrobial properties, and it is commonly used as a fragrance ingredient in personal care products and as a flavoring agent in food. Norcamphorol is also utilized as a precursor for the synthesis of various other compounds, including pharmaceuticals and synthetic flavors. Additionally, it has been studied for its potential as a chiral building block in organic synthesis. Overall, norcamphorol is a versatile compound with a range of practical and industrial applications.
Check Digit Verification of cas no
The CAS Registry Mumber 19898-59-0 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 9 respectively.
Calculate Digit Verification of CAS Registry Number 19898-59:
(7*1)+(6*9)+(5*8)+(4*9)+(3*8)+(2*5)+(1*9)=180
180 % 10 = 0
So 19898-59-0 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
19898-59-0Relevant 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)
-
