156-06-9 | Benzenepropanoic acid, α-oxo-

Packsize	Purity	Availability	Price	Discounted Price
500mg	93%	in stock	$30.00	$21.00
1g	93%	in stock	$34.00	$24.00
5g	93%	in stock	$82.00	$57.00
25g	93%	in stock	$248.00	$174.00

Description

• Catalog Number: AA78111
• Chemical Name: Benzenepropanoic acid, α-oxo-
• CAS Number: 156-06-9
• Molecular Formula: C9H8O3
• Molecular Weight: 164.15802
• MDL Number: MFCD00002589
• SMILES: O=C(C(=O)O)Cc1ccccc1

Computed Properties

• Complexity: 180
• Covalently-Bonded Unit Count: 1
• Heavy Atom Count: 12
• Hydrogen Bond Acceptor Count: 3
• Hydrogen Bond Donor Count: 1
• Rotatable Bond Count: 3
• XLogP3: 1.3

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  Journal of chromatography. B, Biomedical sciences and applications 20010705

• Regioselective dimerization of ferulic acid in a micellar solution.

  Journal of agricultural and food chemistry 20010701

• Novel biomarkers of the metabolism of caffeic acid derivatives in vivo.

  Free radical biology & medicine 20010601

• Isolation and characterization of human colonic bacteria able to hydrolyse chlorogenic acid.

  Journal of applied microbiology 20010601

• Tyrosine and phenylalanine catabolism by Lactobacillus cheese flavor adjuncts.

  Journal of dairy science 20010501

• Shifting the biotransformation pathways of L-phenylalanine into benzaldehyde by Trametes suaveolens CBS 334.85 using HP20 resin.

  Letters in applied microbiology 20010401

• LC/ES-MS detection of hydroxycinnamates in human plasma and urine.

  Journal of agricultural and food chemistry 20010401

• Impaired arachidonic (20:4n-6) and docosahexaenoic (22:6n-3) acid synthesis by phenylalanine metabolites as etiological factors in the neuropathology of phenylketonuria.

  Molecular genetics and metabolism 20010301

• Enzymes involved in hydroxycinnamate metabolism.

  Methods in enzymology 20010101

• The emerging periplasm-localized subclass of AroQ chorismate mutases, exemplified by those from Salmonella typhimurium and Pseudomonas aeruginosa.

  Genome biology 20010101