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・ Phenyl-2-nitropropene
・ Phenyl-C61-butyric acid methyl ester
・ Phenyl-D-galactopyranoside
・ Phenylacetaldehyde
・ Phenylacetaldehyde dehydrogenase
・ Phenylacetaldoxime dehydratase
・ Phenylacetate
・ Phenylacetate—CoA ligase
・ Phenylacetic acid
・ Phenylacetone
・ Phenylacetone monooxygenase
・ Phenylacetones
・ Phenylacetyl-CoA 1,2-epoxidase
・ Phenylacetyl-CoA dehydrogenase
・ Phenylacetyl-CoA hydrolase
Phenylacetylcarbinol
・ Phenylacetylene
・ Phenylacetylglutamine
・ Phenylahistin
・ Phenylalanine
・ Phenylalanine (data page)
・ Phenylalanine 2-monooxygenase
・ Phenylalanine adenylyltransferase
・ Phenylalanine ammonia-lyase
・ Phenylalanine decarboxylase
・ Phenylalanine dehydrogenase
・ Phenylalanine hydroxylase
・ Phenylalanine N-acetyltransferase
・ Phenylalanine N-monooxygenase
・ Phenylalanine racemase (ATP-hydrolysing)


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Phenylacetylcarbinol : ウィキペディア英語版
Phenylacetylcarbinol

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Phenylacetylcarbinol (PAC) is an organic compound that has two enantiomers, one with R- and one with S-configuration. (R)-PAC, which is commonly called -PAC, is known as a precursor in the synthesis of pharmaceuticals such as ephedrine and pseudoephedrine.
== Nomenclature ==

(R)-PAC or (R)-(−)-phenylacetylcarbinol is identical to -PAC, referring to the outdated .
〔Rosche et al. (''Biotransformation of benzaldehyde into (R)-phenylacetylcarbinol by filamentous fungi or their extracts'' ) Appl Microbiol and Biotechnol; Vol. 57, Nr 3 (2001), pp 309-315; 〕
(R)-PAC is the levo-rotating isomer of phenylacetylcarbinol.
The IUPAC name of phenylacetylcarbinol is 1-hydroxy-1-phenylpropan-2-one. Synonyms are 1-hydroxy-1-phenyl-2-propanone and 1-Hydroxy-1-phenylacetone.

抄文引用元・出典: フリー百科事典『 ウィキペディア(Wikipedia)
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