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Details

Stereochemistry ABSOLUTE
Molecular Formula C23H27NO5
Molecular Weight 397.4642
Optical Activity UNSPECIFIED
Defined Stereocenters 2 / 2
E/Z Centers 0
Charge 0

SHOW SMILES / InChI
Structure of Fmoc-O-tert-butyl-L-allothreonine

SMILES

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

InChI

InChIKey=LZOLWEQBVPVDPR-XOBRGWDASA-N
InChI=1S/C23H27NO5/c1-14(29-23(2,3)4)20(21(25)26)24-22(27)28-13-19-17-11-7-5-9-15(17)16-10-6-8-12-18(16)19/h5-12,14,19-20H,13H2,1-4H3,(H,24,27)(H,25,26)/t14-,20-/m0/s1

HIDE SMILES / InChI

Molecular Formula C23H27NO5
Molecular Weight 397.4642
Charge 0
Count
Stereochemistry ABSOLUTE
Additional Stereochemistry No
Defined Stereocenters 2 / 2
E/Z Centers 0
Optical Activity UNSPECIFIED

Approval Year

Substance Class Chemical
Created
by admin
on Sat Dec 16 19:33:58 GMT 2023
Edited
by admin
on Sat Dec 16 19:33:58 GMT 2023
Record UNII
WEF7D6K6AF
Record Status Validated (UNII)
Record Version
  • Download
Name Type Language
Fmoc-O-tert-butyl-L-allothreonine
Common Name English
N-(((9H-fluoren-9-yl)methoxy)carbonyl)-O-(tert-butyl)-L-allothreonine
Common Name English
O-(1,1-Dimethylethyl)-N-[(9H-fluoren-9-ylmethoxy)carbonyl]-L-allothreonine
Common Name English
L-Allothreonine, O-(1,1-dimethylethyl)-N-[(9H-fluoren-9-ylmethoxy)carbonyl]-
Common Name English
O-(tert-Butyl)-N-Fmoc-L-allothreonine
Common Name English
(2S,3S)-2-(9H-fluoren-9-ylmethoxycarbonylamino)-3-[(2-methylpropan-2-yl)oxy]butanoic acid
Common Name English
(2S,3S)-2-((((9H-fluoren-9-yl)methoxy)carbonyl)amino)-3-(tert-butoxy)butanoic acid
Systematic Name English
Code System Code Type Description
CAS
201481-37-0
Created by admin on Sat Dec 16 19:33:58 GMT 2023 , Edited by admin on Sat Dec 16 19:33:58 GMT 2023
PRIMARY
FDA UNII
WEF7D6K6AF
Created by admin on Sat Dec 16 19:33:58 GMT 2023 , Edited by admin on Sat Dec 16 19:33:58 GMT 2023
PRIMARY
EPA CompTox
DTXSID50369199
Created by admin on Sat Dec 16 19:33:58 GMT 2023 , Edited by admin on Sat Dec 16 19:33:58 GMT 2023
PRIMARY
PUBCHEM
2724634
Created by admin on Sat Dec 16 19:33:58 GMT 2023 , Edited by admin on Sat Dec 16 19:33:58 GMT 2023
PRIMARY
Related Record Type Details
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