3917-39-3 Usage
Description
(2E,4E)-β-Ionyliden-ethanol, with the CAS number 3917-39-3, is a compound that is characterized as a yellow oil. It is primarily known for its utility in organic synthesis, making it a valuable component in the creation of various chemical products.
Uses
Used in Organic Synthesis:
(2E,4E)-β-Ionyliden-ethanol is used as a key intermediate in the synthesis of various organic compounds. Its unique chemical structure allows it to participate in a range of reactions, facilitating the formation of complex molecules and contributing to the development of new materials and products in the chemical industry.
Used in Pharmaceutical Industry:
In the pharmaceutical industry, (2E,4E)-β-Ionyliden-ethanol is used as a building block for the development of novel drugs. Its chemical properties make it suitable for the creation of new medicinal compounds, potentially leading to the discovery of innovative treatments for various diseases and conditions.
Used in Fragrance Industry:
(2E,4E)-β-Ionyliden-ethanol is also utilized in the fragrance industry as a component in the creation of unique and complex scents. Its distinctive chemical profile can contribute to the development of new perfumes and fragrances, enhancing the sensory experience for consumers.
Used in Chemical Research:
In the field of chemical research, (2E,4E)-β-Ionyliden-ethanol serves as a valuable compound for studying various reaction mechanisms and exploring new areas of chemical science. Its unique properties and reactivity make it an interesting subject for researchers, potentially leading to new discoveries and advancements in the field.
Check Digit Verification of cas no
The CAS Registry Mumber 3917-39-3 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 3,9,1 and 7 respectively; the second part has 2 digits, 3 and 9 respectively.
Calculate Digit Verification of CAS Registry Number 3917-39:
(6*3)+(5*9)+(4*1)+(3*7)+(2*3)+(1*9)=103
103 % 10 = 3
So 3917-39-3 is a valid CAS Registry Number.
InChI:InChI=1/C15H24O/c1-12(9-11-16)7-8-14-13(2)6-5-10-15(14,3)4/h7-9,16H,5-6,10-11H2,1-4H3/b8-7+,12-9+
3917-39-3Relevant articles and documents
INCORPORATION OF α-IONYLIDENE ETHANOL AND α-IONYLIDENE ACETIC ACID INTO ABSCISIC ACID BY CERCOSPORA ROSICOLA
Neill, Steven J.,Horgan, Roger
, p. 2469 - 2472 (1983)
2H-Labelled α-ionylidene ethanol and α-ionylidene acetic acid are converted in high yield to 1'-deoxy-abscisic acid (1'-deoxy-ABA) and abscisic acid (ABA) by Cercospora rosicola.Incorporation of label was confirmed by mass spectrometry.The 2-trans isomers
Agents for use on skin and/or hair containing quadruply substituted cyclohexene compounds
-
Page/Page column 12-13, (2010/11/28)
The invention relates to agents for use on skin or hair, particularly for increasing skin tanning and the synthesis of melanin in skin or hair. The invention contains, in particular, cosmetic or dermatological preparations containing quadruply substituted
Palladium-catalyzed coupling reaction of an enol nonaflate with (vinyl)tributylstannanes and acetylenes: A highly stereoselective synthesis of 8,18-13C2-labeled retinal
Wada, Akimori,Ieki, Yasuhiro,Nakamura, Saeko,Ito, Masayoshi
, p. 1581 - 1588 (2007/10/03)
Here we report that enol nonaflates exhibit higher reactivity than the corresponding enol triflates in palladium-catalyzed cross-coupling reactions with various (vinyl)tributylstannanes and acetylenes. We also highlight the reaction of a vinyl nonaflate,
