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L-[3R-2H]-PHENYLALANINE

Compound with spectra: 1 NMR

L-[3R-2H]-PHENYLALANINE
SpectraBase Compound ID BAjw2kWb756
InChI InChI=1S/C9H11NO2/c10-8(9(11)12)6-7-4-2-1-3-5-7/h1-5,8H,6,10H2,(H,11,12)/t8-/m0/s1/i6D/t6-,8+/m1
InChIKey COLNVLDHVKWLRT-HTUZQGSXSA-N
Mol Weight 166.2 g/mol
Molecular Formula C9H102HNO2
Exact Mass 166.085255 g/mol
Enantiomer InChIKey COLNVLDHVKWLRT-GOTMFYRJSA-N
Racemate InChIKey COLNVLDHVKWLRT-RAMDWTOOSA-N

View Spectrum of L-[3R-2H]-PHENYLALANINE

13C NMR Spectrum
Copyright Copyright © 2016-2024 W. Robien, Inst. of Org. Chem., Univ. of Vienna. All Rights Reserved.
Solvent D2O
L-Phenylalanine
(2S)-[2-2H]-PHENYLALANINE
D-Phenylalanine
Phenylalanine cation
L-[3-13C]phenylalanine hydrochloride
(2S,3S)-[3-(2)H-1]-PHENYLALANINE
Alanine-2-d, 3-phenyl-, L-
L-[2,3S-2H2]-PHENYLALANINE
DL-Phenylalanine
DL-3-PHENYLALANINE, HYDROCHLORIDE
DL-3-PHENYLALANINE, HYDROBROMIDE
3-Deuterio-2-methyl-3-phenylpropionic acid
1-Phenyl-1,2-dideuteriopropanoic acid
alpha,beta-diaminohydrocinnamic acid
beta-Methyl-DL-phenylalanine hydrochloride
DL-3-phenylserine, hydrated, sodium salt
(2S,3S)-(+)-3-FLUOROPHENYLALANINE
3-phenylserine
DL-threo-β-Phenylserine
AMPHETAMINE;DIDEUTERATED
alpha,beta-DIMETHYLHYDROCINNAMIC ACID
Title Journal or Book Year
Biosynthetic Studies of ω-Cycloheptyl Fatty Acids in Alicyclobacillus cycloheptanicus. Formation of Cycloheptanecarboxylic Acid from Phenylacetic Acid The Journal of Organic Chemistry 1997
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