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Details

Stereochemistry ABSOLUTE
Molecular Formula C28H29NO5
Molecular Weight 459.5336
Optical Activity ( + )
Defined Stereocenters 1 / 1
E/Z Centers 0
Charge 0

SHOW SMILES / InChI
Structure of Fmoc-D-Tyr(tBu)-OH

SMILES

CC(C)(C)OC1=CC=C(C[C@@H](NC(=O)OCC2C3=CC=CC=C3C4=CC=CC=C24)C(O)=O)C=C1

InChI

InChIKey=JAUKCFULLJFBFN-RUZDIDTESA-N
InChI=1S/C28H29NO5/c1-28(2,3)34-19-14-12-18(13-15-19)16-25(26(30)31)29-27(32)33-17-24-22-10-6-4-8-20(22)21-9-5-7-11-23(21)24/h4-15,24-25H,16-17H2,1-3H3,(H,29,32)(H,30,31)/t25-/m1/s1

HIDE SMILES / InChI

Molecular Formula C28H29NO5
Molecular Weight 459.5336
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 19:23:50 GMT 2025
Edited
by admin
on Wed Apr 02 19:23:50 GMT 2025
Record UNII
8L4C2S5DL6
Record Status Validated (UNII)
Record Version
  • Download
Name Type Language
(2R)-2-(9H-Fluoren-9-ylmethoxycarbonylamino)-3-[4-[(2-methylpropan-2-yl)oxy]phenyl]propanoic acid
Preferred Name English
Fmoc-D-Tyr(tBu)-OH
Common Name English
(R)-2-((((9H-Fluoren-9-yl)methoxy)carbonyl)amino)-3-(4-(tert-butoxy)phenyl)propanoic acid
Systematic Name English
O-(1,1-Dimethylethyl)-N-[(9H-fluoren-9-ylmethoxy)carbonyl]-D-tyrosine
Systematic Name English
D-Tyrosine, O-(1,1-dimethylethyl)-N-[(9H-fluoren-9-ylmethoxy)carbonyl]-
Systematic Name English
Code System Code Type Description
EPA CompTox
DTXSID50922687
Created by admin on Wed Apr 02 19:23:50 GMT 2025 , Edited by admin on Wed Apr 02 19:23:50 GMT 2025
PRIMARY
FDA UNII
8L4C2S5DL6
Created by admin on Wed Apr 02 19:23:50 GMT 2025 , Edited by admin on Wed Apr 02 19:23:50 GMT 2025
PRIMARY
CAS
118488-18-9
Created by admin on Wed Apr 02 19:23:50 GMT 2025 , Edited by admin on Wed Apr 02 19:23:50 GMT 2025
PRIMARY
PUBCHEM
12968135
Created by admin on Wed Apr 02 19:23:50 GMT 2025 , Edited by admin on Wed Apr 02 19:23:50 GMT 2025
PRIMARY
Related Record Type Details
RACEMATE -> ENANTIOMER
ENANTIOMER -> ENANTIOMER