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Details

Stereochemistry ABSOLUTE
Molecular Formula C20H21NO4
Molecular Weight 339.385
Optical Activity ( - )
Defined Stereocenters 1 / 1
E/Z Centers 0
Charge 0

SHOW SMILES / InChI
Structure of Fmoc-L-Val-OH

SMILES

CC(C)[C@H](NC(=O)OCC1C2=CC=CC=C2C3=CC=CC=C13)C(O)=O

InChI

InChIKey=UGNIYGNGCNXHTR-SFHVURJKSA-N
InChI=1S/C20H21NO4/c1-12(2)18(19(22)23)21-20(24)25-11-17-15-9-5-3-7-13(15)14-8-4-6-10-16(14)17/h3-10,12,17-18H,11H2,1-2H3,(H,21,24)(H,22,23)/t18-/m0/s1

HIDE SMILES / InChI

Molecular Formula C20H21NO4
Molecular Weight 339.385
Charge 0
Count
Stereochemistry ABSOLUTE
Additional Stereochemistry No
Defined Stereocenters 1 / 1
E/Z Centers 0
Optical Activity UNSPECIFIED

Approval Year

Substance Class Chemical
Created
by admin
on Wed Apr 02 20:24:06 GMT 2025
Edited
by admin
on Wed Apr 02 20:24:06 GMT 2025
Record UNII
S9C32XT8YE
Record Status Validated (UNII)
Record Version
  • Download
Name Type Language
NSC-334304
Preferred Name English
Fmoc-L-Val-OH
Common Name English
(2S)-2-[[[(9H-Fluoren-9-yl)methoxy]carbonyl]amino]-3-methylbutanoic acid
Systematic Name English
N-[(9H-Fluoren-9-ylmethoxy)carbonyl]-L-valine
Systematic Name English
FMOC-L-valine
Common Name English
(S)-N-Fmoc-valine
Common Name English
(S)-2-(9H-Fluoren-9-ylmethoxycarbonylamino)-3-methylbutanoic acid
Systematic Name English
N-(9-Fluorenylmethoxycarbonyl)-L-valine
Systematic Name English
L-Valine, N-[(9H-fluoren-9-ylmethoxy)carbonyl]-
Systematic Name English
(9-Fluorenylmethoxycarbonyl)valine
Common Name English
Fmoc-Val-OH
Common Name English
Code System Code Type Description
PUBCHEM
688217
Created by admin on Wed Apr 02 20:24:06 GMT 2025 , Edited by admin on Wed Apr 02 20:24:06 GMT 2025
PRIMARY
FDA UNII
S9C32XT8YE
Created by admin on Wed Apr 02 20:24:06 GMT 2025 , Edited by admin on Wed Apr 02 20:24:06 GMT 2025
PRIMARY
CAS
68858-20-8
Created by admin on Wed Apr 02 20:24:06 GMT 2025 , Edited by admin on Wed Apr 02 20:24:06 GMT 2025
PRIMARY
EPA CompTox
DTXSID901317560
Created by admin on Wed Apr 02 20:24:06 GMT 2025 , Edited by admin on Wed Apr 02 20:24:06 GMT 2025
PRIMARY
Related Record Type Details
ENANTIOMER -> ENANTIOMER
RACEMATE -> ENANTIOMER