36237-66-8 Usage
Uses
Used in Pheromone Applications:
(6E,10E,R)-3,7,11,15-Tetramethyl-6,10,14-hexadecatrien-1-ol is used as a pheromone component in the labial gland secretion of cuckoo-bumblebee (Psithyrus vestalis) males. It plays a crucial role in the chemical communication and mating behavior of these insects, helping them to attract and locate potential mates.
Used in Chemical Ecology Research:
(6E,10E,R)-3,7,11,15-Tetramethyl-6,10,14-hexadecatrien-1-ol is also used in chemical ecology research to study the chemical signals and communication mechanisms in insects. Understanding the role of (6E,10E,R)-3,7,11,15-Tetramethyl-6,10,14-hexadecatrien-1-ol in insect behavior can provide valuable insights into their ecology, reproduction, and interactions with other species.
Used in Fragrance Industry:
Due to its unique and pleasant aroma, (6E,10E,R)-3,7,11,15-Tetramethyl-6,10,14-hexadecatrien-1-ol can be used as a fragrance ingredient in the perfumery and cosmetics industry. Its natural origin and distinctive scent make it a valuable addition to various fragrance formulations.
Used in Flavor Industry:
(6E,10E,R)-3,7,11,15-Tetramethyl-6,10,14-hexadecatrien-1-ol can also be used as a flavoring agent in the food and beverage industry. Its unique taste and aroma can enhance the flavor profiles of various products, adding a natural and appealing note to them.
Check Digit Verification of cas no
The CAS Registry Mumber 36237-66-8 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 3,6,2,3 and 7 respectively; the second part has 2 digits, 6 and 6 respectively.
Calculate Digit Verification of CAS Registry Number 36237-66:
(7*3)+(6*6)+(5*2)+(4*3)+(3*7)+(2*6)+(1*6)=118
118 % 10 = 8
So 36237-66-8 is a valid CAS Registry Number.
36237-66-8Relevant academic research and scientific papers
A Unified Approach for the Total Synthesis of cyclo-Archaeol, iso-Caldarchaeol, Caldarchaeol, and Mycoketide
Andringa, Ruben L. H.,Driessen, Arnold J. M.,Minnaard, Adriaan J.,de Kok, Niels A. W.
supporting information, p. 17497 - 17503 (2021/06/08)
Ir-catalyzed asymmetric alkene hydrogenation is presented as the strategy par excellence to prepare saturated isoprenoids and mycoketides. This highly stereoselective synthesis approach is combined with an established 13C-NMR method to determine the enantioselectivity of each methyl-branched stereocenter. It is shown that this analysis is fit for purpose and the combination allows the synthesis of the title compounds with a significant increase in efficiency.
Analysis of the labial gland secretion of the cuckoo-bumblebee (Psithyrus vestalis) males and synthesis of abundant geranylcitronellol
Valterova, Irena,Svatos, Ales,Hovorka, Oldrich
, p. 1501 - 1508 (2007/10/03)
Labial glands of the cuckoo-bumblebee males of the species Psithyrus vestalis were extracted and the components of their secretions were identified. Chemical composition of the males' signal of Psithyrus vestalis has not yet been described in the literatu
A short and selective synthesis of (S)-geranylcitronellol via conjugate addition of a functionalized copper reagent to 2-substituted exo-bornyl crotonates
Johansson, Anders,Olsson, Thomas,Bergstroem, Gunnar
, p. 7127 - 7128 (2007/10/03)
An asymmetric synthesis of the diterpene (S)-geranylcitronellol 1a and its acetate 1b is reported. The chirality is induced by TMSI-promoted conjugate addition of a homoallylic monoorganocopper reagent to 2-naphthyl-exo-bornylcrotonate, which proceeds wit
