6033-23-4 Usage
Description
(S)-(+)-2-Heptanol, also known as (2S)-2-hydroxyheptane, is a secondary alcohol with a hydroxy group at the second carbon of the heptane chain. It exists as the 2S-stereoisomer and is characterized by its colorless to light yellow liquid appearance. This organic compound is known for its distinct chemical properties and versatile applications across various industries.
Uses
Used in Pharmaceutical Industry:
(S)-(+)-2-Heptanol is used as a pharmaceutical intermediate for the synthesis of various drugs and medications. Its unique chemical structure allows it to serve as a building block in the development of new pharmaceutical compounds, contributing to the advancement of medical treatments and therapies.
Used in Flavor and Fragrance Industry:
(S)-(+)-2-Heptanol, due to its distinct chemical properties, is also utilized in the flavor and fragrance industry. It can be used to create specific scents or enhance the aroma of various products, such as perfumes, cosmetics, and household items.
Used in Chemical Synthesis:
In the field of chemical synthesis, (S)-(+)-2-Heptanol serves as a valuable intermediate for the production of other organic compounds. Its versatility in chemical reactions makes it a useful component in the synthesis of various chemicals, including specialty chemicals and materials.
Used in Research and Development:
(S)-(+)-2-Heptanol is also employed in research and development settings, where it can be used to study the properties and behavior of secondary alcohols and their stereoisomers. This knowledge can be applied to the development of new compounds and materials with specific characteristics and applications.
Check Digit Verification of cas no
The CAS Registry Mumber 6033-23-4 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 6,0,3 and 3 respectively; the second part has 2 digits, 2 and 3 respectively.
Calculate Digit Verification of CAS Registry Number 6033-23:
(6*6)+(5*0)+(4*3)+(3*3)+(2*2)+(1*3)=64
64 % 10 = 4
So 6033-23-4 is a valid CAS Registry Number.
InChI:InChI=1/C7H16O/c1-3-4-5-6-7(2)8/h7-8H,3-6H2,1-2H3
6033-23-4Relevant articles and documents
Co-immobilized Whole Cells with ω-Transaminase and Ketoreductase Activities for Continuous-Flow Cascade Reactions
Nagy-Gy?r, László,Abaházi, Emese,Bódai, Viktória,Sátorhelyi, Péter,Erdélyi, Balázs,Balogh-Weiser, Diána,Paizs, Csaba,Hornyánszky, Gábor,Poppe, László
, p. 1845 - 1848 (2018/09/10)
An improved sol–gel process involving the use of hollow silica microspheres as a supporting additive was applied for the co-immobilization of whole cells of Escherichia coli with Chromobacterium violaceum ω-transaminase activity and Lodderomyces elongisporus with ketoreductase activity. The co-immobilized cells with two different biocatalytic activities could perform a cascade of reactions to convert racemic 4-phenylbutan-2-amine or heptan-2-amine into a nearly equimolar mixture of the corresponding enantiomerically pure R amine and S alcohol even in continuous-flow mode. The novel co-immobilized whole-cell system proved to be an easy-to-store and durable biocatalyst.
ALKANE OXIDATION BY MODIFIED HYDROXYLASES
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Paragraph 0323; 0324, (2016/02/16)
This invention relates to modified hydroxylases. The invention further relates to cells expressing such modified hydroxylases and methods of producing hydroxylated alkanes by contacting a suitable substrate with such cells.
A novel P450-based biocatalyst for the selective production of chiral 2-alkanols
Von Bühler, Clemens J.,Urlacher, Vlada B.
supporting information, p. 4089 - 4091 (2014/04/03)
A P450 monooxygenase from Nocardia farcinica (CYP154A8) catalyses the stereo- and regioselective hydroxylation of n-alkanes, still a challenging task in chemical catalysis. In a biphasic reaction system, the regioselectivity for the C2-position of C7-C9 alkanes was over 90%. The enzyme showed strict S-selectivity for all tested substrates, with enantiomeric excess (ee) of up to 91%. This journal is the Partner Organisations 2014.