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(S)-2-hydroxyvaleric acid
Basic Information
- CAS No.: 41014-93-1
Physical properties
Product Description
Quality products?make an important contribution to long-term revenue and profitability. Factory supply good quality (S)-2-hydroxyvaleric acid 41014-93-1 with stock
1.What is the (S)-2-hydroxyvaleric acid ?
(S)-2-hydroxyvaleric acid, also known as (S)-2-hydroxypentanoic acid, is a specific isomer of 2-hydroxyvaleric acid, distinguished by the spatial orientation of its molecular structure. It is an organic compound and a type of beta-hydroxy acid. This chemical features a carboxylic acid group (-COOH) and a hydroxyl group (-OH), with the hydroxyl group attached to the second carbon atom in the pentanoic acid chain, hence the '2' in its name.
2.What is the CAS number for (S)-2-hydroxyvaleric acid ?
The CAS number of (S)-2-hydroxyvaleric acid is 41014-93-1.
3.What are another words for (S)-2-hydroxyvaleric acid ?
Synonyms?for?(S)-2-hydroxyvaleric acid 41014-93-1:Pentanoicacid, 2-hydroxy-, (S)-;(S)-2-Hydroxyvaleric acid;(S)-a-Hydroxyvaleric acid;L-2-Hydroxypentanoic acid;L-2-Hydroxyvaleric acid;S-2-Hydroxypentanoic acid;
4.What is (S)-2-hydroxyvaleric acid (41014-93-1) used for?
Used in Chemical Synthesis:
(S)-2-hydroxyvaleric acid is used as a building block for the production of other complex organic compounds. Its unique structure allows it to be a key component in the synthesis of various molecules, making it valuable in the field of organic chemistry.
Used in Scientific Research:
(S)-2-hydroxyvaleric acid is used as a research compound for studying the properties and reactions of beta-hydroxy acids. Its distinct isomerism provides insights into the effects of molecular structure on chemical behavior and reactivity.
Used in Manufacturing Processes:
(S)-2-hydroxyvaleric acid is used as an intermediate in the production of various industrial chemicals and materials. Its versatility in chemical reactions makes it a useful component in the manufacturing of a wide range of products.
InChI:InChI=1/C5H10O3/c1-2-3-4(6)5(7)8/h4,6H,2-3H2,1H3,(H,7,8)/t4-/m0/s1
Relevant articles related to (S)-2-hydroxyvaleric acid:
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Article |
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Enzymatic Resolution by a d-Lactate Oxidase Catalyzed Reaction for (S)-2-Hydroxycarboxylic Acids |
Sheng, Binbin,Xu, Jing,Ge, Yongsheng,Zhang, Shuo,Wang, Danqi,Gao, Chao,Ma, Cuiqing,Xu, Ping , p. 2630 - 2633 (2016/08/30) |
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Efficient intramolecular asymmetric reductions of α-, β-, and γ-keto acids with diisopinocampheylborane1 |
Veeraraghavan Ramachandran,Brown, Herbert C.,Pitre, Sangeeta , p. 17 - 18 (2007/10/03) |
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Asymmetric reactions of α-ketoacid-derived hemiacetals: Stereoselective synthesis of α-hydroxy acids |
Pansare, Sunil V.,Ravi, R. Gnana , p. 14549 - 14564 (2007/10/03) |
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