79516-59-9

Basic information

• Product Name: Pentanoic acid, 3-hydroxy-, (S)-
• CAS NO: 79516-59-9
• Molecular Formula: C5H10O3
• Molecular Weight: 118.133
• Mol File: 79516-59-9.mol
• Article Data: 12

Chemical Properties

• CAS DataBase Reference: Pentanoic acid, 3-hydroxy-, (S)-(CAS DataBase Reference)
• NIST Chemistry Reference: Pentanoic acid, 3-hydroxy-, (S)-(79516-59-9)
• EPA Substance Registry System: Pentanoic acid, 3-hydroxy-, (S)-(79516-59-9)

Safety Data

• Hazardous Substances Data: 79516-59-9(Hazardous Substances Data)

Upstream product

• 13635-05-7 3-hydroxyvaleronitrile 
• 4949-44-4 ethyl propanoylacetate 
• 13991-37-2 trans-2-pentenoic acid 
• 20603-44-5 3,5-O-Benzylidene-D-ribonic Acid γ-Lactone 
• 141-82-2 malonic acid 
• 123-38-6 propionaldehyde 
• 54074-85-0 ethyl-3-hydroxypentanoate 
• 62959-96-0 (S)-(-)-hex-5-en-3-ol 
• 1372762-98-5 C₉H₁₇NO₃S 
• 64074-05-1 2,2-dimethyl-5-propanoyl-1,3-dioxan-4,6-dione 
• 437614-61-4 3-oxopentanoyl-N-acetylcysteamine thioester 
• 30414-53-0 methyl propanoyl acetate 
• 5461-96-1 ammonium D-xylonate 
• 98269-11-5 (S)-3-Hydroxy-pentanoic acid (1R,4S)-3-[benzenesulfonyl-(3,5-dimethyl-phenyl)-amino]-1,7,7-trimethyl-bicyclo[2.2.1]hept-2-yl ester 

Downstream Products

• 10191-25-0 3-oxo-valeric acid 
• 626-98-2 pent-2-enoic acid 
• 5204-64-8 3-pentenoic acid 
• 129705-30-2 (3S,6S)-3,6-dihydroxy-2,7-dimethyloctane 
• 136705-66-3 (3S,6S)-octane-3,6-diol 
• 124-38-9 carbon dioxide 
• 7732-18-5 water 
• 802294-64-0 propionic acid 
• 137151-97-4 (2R,5R)-2,5-diisopropyl-1-phenylphospholane 

Relevant articles and documents

General chemoenzymatic route to two-stereocenter triketides employing assembly line ketoreductases

Modular polyketide synthases (PKSs) are enzymatic assembly lines that fuse carbon fragments into complex chiral products. Here, their synthetic logic is employed to chemoenzymatically generate two-stereocenter triketides. Each of the four stereoisomers was constructed in a stereocontrolled manner using C-acylation and two PKS ketoreductases possessing opposite stereoselectivities.

A study of the reaction of n-BuLi with Ti(Oi-Pr)4 as a method to generate titanacyclopropane and titanacyclopropene species

The use of the combination of reagents Ti(Oi-Pr)4/n-BuLi, introduced by the group of J.J. Eisch in 2001, has only found a few applications so far, with sometimes conflicting observations. This article describes a study aimed at clarifying the nature, the stability and the reactivity of the active organometallic species involved. Reactions with CO2 and other trapping reagents reveal that it is generated within a few minutes at 0 C in THF, where it can be considered to be stable for 30 min. Most of our results are consistent with the expected titanacyclopropane nature of this reagent but some observations suggest that the chemistry at play may be more complicated.

PHA E and PHA C components of poly(hydroxy fatty acid) synthase from thiocapsa pfennigii

PCT No. PCT/DE95/01279 Sec. 371 Date Jul. 3, 1997 Sec. 102(e) Date Jul. 3, 1997 PCT Filed Sep. 15, 1995 PCT Pub. No. WO96/08566 PCT Pub. Date Mar. 21, 1996The present invention relates to a process for the production of poly (hydroxy fatty acids) as well as recombinant bacterial strains for carrying out the process. In addition, new poly(hydroxy fatty acids) and new substrates for the production of conventional and new poly(hydroxy fatty acids) are described. Moreover, the invention also relates to a DNA fragment, which codes for a PhaE and a PhaC component of the poly(hydroxy fatty acid) synthase from Thiocapsa pfennigii, as well as the corresponding poly (hydroxy fatty acid) synthase protein.