90192-96-4 Usage
Description
[S,(+)]-4-Heptyne-2-ol, with the molecular formula C7H12O, is a chemical compound that exists as an enantiomer of 4-heptyne-2-ol. This means it has a chiral center and is available in two non-superimposable mirror-image forms. It is recognized for its ability to participate in a range of chemical reactions, such as oxidation, reduction, and alkyne coupling, which contribute to its diverse applications.
Uses
Used in Organic Synthesis:
[S,(+)]-4-Heptyne-2-ol is utilized as a reagent in organic synthesis, where its capacity to undergo various chemical reactions makes it a valuable component in creating different compounds.
Used in Pharmaceutical Production:
[S,(+)]-4-Heptyne-2-ol is also employed in the production of pharmaceuticals, where its unique properties can be harnessed to develop new drugs with specific therapeutic effects.
Used in Agrochemicals:
[S,(+)]-4-Heptyne-2-ol finds application in the agrochemical industry, potentially contributing to the development of new pesticides or other agricultural chemicals that can enhance crop protection and yield.
Used in Flavor and Fragrance Industry:
Its utilization extends to the flavor and fragrance sector, where it may be used to create or modify scents and tastes in various consumer products.
Used in Antimicrobial Applications:
[S,(+)]-4-Heptyne-2-ol has been investigated for its potential antibacterial and antifungal properties, suggesting that it could be used in the development of new antimicrobial agents to combat infections.
Check Digit Verification of cas no
The CAS Registry Mumber 90192-96-4 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 9,0,1,9 and 2 respectively; the second part has 2 digits, 9 and 6 respectively.
Calculate Digit Verification of CAS Registry Number 90192-96:
(7*9)+(6*0)+(5*1)+(4*9)+(3*2)+(2*9)+(1*6)=134
134 % 10 = 4
So 90192-96-4 is a valid CAS Registry Number.
90192-96-4Relevant articles and documents
Synthesis and biological evaluation of 12-, 13-, 14-membered macrolides and open chain 2,6-trans-disubstituted dihydropyran analogues for aspergillides
Pabbaraja, Srihari,Gantasala, Naresh,Ydhyam, Sridhar,Namballa, Hari Krishna,Gundeboina, Subhashini,Lambu, Mallikharjuna R.,Meena, Sanjeev,Datta, Dipak
, p. 2570 - 2576 (2018/05/30)
Stereoselective synthesis of twenty (three 12-, five 13- and twelve 14-membered) macrolides and seventeen functionalized 2,6-trans-disubstituted dihydropyran derivatives have been achieved. The key reactions include an Achmatowicz rearrangement, Ferrier-type alkynylation, Yamaguchi macrolactonization and Lindlar's hydrogenation. Biological screening of the synthesised compounds showed moderate activity against human cancer cell-lines.
Total synthesis of (+)-brefeldin a
Wu, Yikang,Gao, Jian
supporting information; experimental part, p. 1533 - 1536 (2009/04/12)
(+)-Brefeldin A was synthesized through an efficient route, which features (1) construction of the five-membered ring from a Crimmins aldol via tandem Li-I exchange and carbanion-mediated cyclization with concurrent removal of the chiral auxiliary, (2) introduction of the lower side chain (C10 to C16) via a Rh-catalyzed Michael addition of a vinyl boronic acid, (3) stereoselective reduction of the C7 ketone with Sml2, and (4) a 2-methyl-6- nitrobenzoic anhydride-mediated (Shiina) lactonization.
Facile synthesis of (+)-Brefeldin A
Nokami,Ohkura,Dan-Oh,Sakamoto
, p. 2409 - 1412 (2007/10/02)
(+)-Brefeldin A (1) was synthesized by using (+)-4-cyanomethylcyclopent-2-en-1-one (2) as a key compound. 4-Hydroxy-2-enoate functionality was built by the reaction of the aldehyde (7) with (S)-ethyl p-chlorophenylsulfinylacetate.
