57648-55-2 Usage
Description
3-Octen-2-ol is an organic compound with a sweet, creamy, buttery, lactone, coconut, coumarin, lavender, and mushroom odor. It is known for its distinct taste characteristics, which include mushroom, green, melon rind, earthy, and nutty notes at a concentration of 20 ppm. 3-OCTEN-2-OL has a CAS No. 57648-55-2 for trans-3-octen-2-ol and is recognized by the FDA PAFA system. FEMA does not distinguish between its isomers.
Uses
Used in Flavor and Fragrance Industry:
3-Octen-2-ol is used as a flavoring agent for its sweet, creamy, and buttery taste characteristics, making it suitable for enhancing the flavor of various food products. Its mushroom, green, melon rind, earthy, and nutty notes contribute to a unique and complex taste profile.
Used in Perfumery:
In the perfumery industry, 3-Octen-2-ol is used as a fragrance ingredient due to its coconut, coumarin, and lavender scent. Its ability to provide a pleasant and long-lasting aroma makes it a valuable addition to perfume compositions.
Used in Aromatherapy:
3-Octen-2-ol's earthy and mushroom notes make it a suitable candidate for use in aromatherapy. Its calming and soothing properties can be beneficial for relaxation and stress relief, promoting a sense of well-being.
Used in Cosmetics:
3-OCTEN-2-OL's unique odor profile can also be utilized in the cosmetics industry, where it can be used to add a distinct and appealing scent to various cosmetic products, such as lotions, creams, and body washes.
Used in the Pharmaceutical Industry:
3-Octen-2-ol's distinct taste and odor characteristics may also find applications in the pharmaceutical industry, where it can be used to mask unpleasant tastes of certain medications or to enhance the overall sensory experience of drug delivery systems.
Check Digit Verification of cas no
The CAS Registry Mumber 57648-55-2 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 5,7,6,4 and 8 respectively; the second part has 2 digits, 5 and 5 respectively.
Calculate Digit Verification of CAS Registry Number 57648-55:
(7*5)+(6*7)+(5*6)+(4*4)+(3*8)+(2*5)+(1*5)=162
162 % 10 = 2
So 57648-55-2 is a valid CAS Registry Number.
57648-55-2Relevant articles and documents
Copper-Catalyzed Enantioselective Conjugate Addition to α,β-Unsaturated Aldehydes with Various Organometallic Reagents
Goncalves-Contal, Sylvie,Gremaud, Ludovic,Palais, La?titia,Babel, Lucille,Alexakis, Alexandre
, p. 3301 - 3308 (2016/09/12)
β-Substituted aldehydes constitute a very important class of compounds found in nature. Synthesis of this motif can be envisioned by C-C bond formation on enals. For this purpose, we report herein the development of enantioselective copper-catalyzed conjugate addition of various organometallic reagents to α,β-unsaturated aldehydes with (R)-H8BINAP, (R)-TolBINAP, and (R)-SEGPHOS as chiral ligands. Three sets of conditions were successfully developed and several enals were used. Reactivity and regio- and enantioselectivities were strongly dependent on reaction conditions and substrates. Good to excellent regio- and enantioselectivities were obtained with zinc reagents R2Zn and aluminum reagents R3Al. However, the asymmetric conjugate addition of Grignard reagents afforded only moderate to good regio- and enantioselectivities.
Rhodium(I) complexes with N-heterocyclic carbenes bearing a 2,3,4,5-tetraphenylphenyl and its higher dendritic frameworks
Sato, Hiromichi,Fujihara, Tetsuaki,Obora, Yasushi,Tokunaga, Makoto,Kiyosu, Junya,Tsuji, Yasushi
, p. 269 - 271 (2007/10/03)
Novel rhodium(i) complexes with N-heterocyclic carbenes bearing a 2,3,4,5-tetraphenylphenyl and its higher dendritic frameworks were synthesized and the complexes were used as catalysts in rhodium-catalyzed hydrosilylation of α,β-unsaturated ketones to show high 1,4-adduct selectivity. The Royal Society of Chemistry.
