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929-48-6

  • Product Name:8-Oxooctanoic acid
  • Molecular Formula:C8H14 O3
  • Molecular Weight:158.197
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Product Details

Purity:99%

Good factory supply good 8-Oxooctanoic acid 929-48-6

  • Molecular Formula:C8H14 O3
  • Molecular Weight:158.197
  • Vapor Pressure:0.000519mmHg at 25°C 
  • Boiling Point:290.4°Cat760mmHg 
  • Flash Point:143.7°C 
  • PSA：54.37000 
  • Density:1.037g/cm3 
  • LogP:1.61050 

7-formylheptanoic acid(Cas 929-48-6) Usage

InChI:InChI=1/C8H14O3/c9-7-5-3-1-2-4-6-8(10)11/h7H,1-6H2,(H,10,11)

929-48-6 Relevant articles

Pharmacokinetics, metabolism and off-target effects in the rat of 8-[(1H- benzotriazol-1-yl)amino]octanoic acid, a selective inhibitor of human cytochrome P450 4Z1: β-oxidation as a potential augmenting pathway for inhibition

Kowalski, John P.,Pelletier, Robert D.,McDonald, Matthew G.,Kelly, Edward J.,Rettie, Allan E.

, p. 901 - 915 (2021)

8‐[(1H‐1,2,3‐benzotriazol‐1‐yl)amino]oct...

Design and characterization of the first selective and potent mechanism-based inhibitor of cytochrome p450 4z1

Kowalski, John P.,Mcdonald, Matthew G.,Pelletier, Robert D.,Hanenberg, Helmut,Wiek, Constanze,Rettie, Allan E.

, p. 4824 - 4836 (2020/06/08)

Mammary-tissue-restricted cytochrome P45...

Regioselective Hydroformylation of Internal and Terminal Alkenes via Remote Supramolecular Control

Linnebank, Pim R.,Ferreira, Stephan Falc?o,Kluwer, Alexander M.,Reek, Joost N. H.

supporting information, p. 8214 - 8219 (2020/06/21)

Regioselective catalytic transformations...

Production of Hydroxy Acids: Selective Double Oxidation of Diols by Flavoprotein Alcohol Oxidase

Fraaije, Marco W.,Martin, Caterina,Trajkovic, Milos

supporting information, p. 4869 - 4872 (2020/02/11)

Flavoprotein oxidases can catalyze oxida...

929-48-6 Process route

8-hydroxycaprylic acid
764-89-6

8-hydroxycaprylic acid

7-formylheptanoic acid
929-48-6

7-formylheptanoic acid

Conditions
Conditions Yield
With 2-iodoxybenzoic acid; In dimethyl sulfoxide; for 4h; Inert atmosphere;
86%
With pyridinium chlorochromate; In dichloromethane; at 20 ℃; for 1h;
30%
With pyridinium chlorochromate; In dichloromethane; at 20 ℃; for 1.5h; Inert atmosphere;
25%
With pyridinium chlorochromate;
With 2,2'-azinobis(3-ethylbenzthiazolinesulfonate); In aq. phosphate buffer; pH=7.4; Enzymatic reaction;
With 1-hydroxy-3H-benz[d][1,2]iodoxole-1,3-dione; In dimethyl sulfoxide; at 20 ℃; for 4h;
7-Formyl-4Z-heptenoic acid
80685-82-1,55348-85-1

7-Formyl-4Z-heptenoic acid

7-formylheptanoic acid
929-48-6

7-formylheptanoic acid

Conditions
Conditions Yield
With hydrogen; palladium on activated charcoal; In acetic acid; at 20 ℃; for 15h; under 15200 Torr;
98%

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929-48-6 Downstream products

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