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Details

Stereochemistry ABSOLUTE
Molecular Formula C26H32N2O6
Molecular Weight 468.5421
Optical Activity ( + )
Defined Stereocenters 1 / 1
E/Z Centers 0
Charge 0

SHOW SMILES / InChI
Structure of N2-Fmoc-N6-BOC-L-lysine

SMILES

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

InChI

InChIKey=UMRUUWFGLGNQLI-QFIPXVFZSA-N
InChI=1S/C26H32N2O6/c1-26(2,3)34-24(31)27-15-9-8-14-22(23(29)30)28-25(32)33-16-21-19-12-6-4-10-17(19)18-11-5-7-13-20(18)21/h4-7,10-13,21-22H,8-9,14-16H2,1-3H3,(H,27,31)(H,28,32)(H,29,30)/t22-/m0/s1

HIDE SMILES / InChI

Molecular Formula C26H32N2O6
Molecular Weight 468.5421
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 Sat Dec 16 19:50:34 GMT 2023
Edited
by admin
on Sat Dec 16 19:50:34 GMT 2023
Record UNII
N8M8CCC7RN
Record Status Validated (UNII)
Record Version
  • Download
Name Type Language
N2-Fmoc-N6-BOC-L-lysine
Common Name English
L-Lysine, N<SUP>6</SUP>-[(1,1-dimethylethoxy)carbonyl]-N<SUP>2</SUP>-[(9H-fluoren-9-ylmethoxy)carbonyl]-
Common Name English
N-α-(Fmoc)-N-ε-(t-boc)-L-Lysine-OH
Common Name English
(S)-2-[[[(9H-Fluoren-9-yl)methoxy]carbonyl]amino]-6-(tert-butoxycarbonylamino)hexanoic acid
Systematic Name English
(2S)-2-(9H-Fluoren-9-ylmethoxycarbonylamino)-6-[(2-methylpropan-2-yl)oxycarbonylamino]hexanoic acid
Systematic Name English
N-α-Fluorenylmethoxycarbonyl-N-ε-tert-butoxycarbonyl-L-lysine
Common Name English
Code System Code Type Description
PUBCHEM
2724628
Created by admin on Sat Dec 16 19:50:34 GMT 2023 , Edited by admin on Sat Dec 16 19:50:34 GMT 2023
PRIMARY
EPA CompTox
DTXSID901316712
Created by admin on Sat Dec 16 19:50:34 GMT 2023 , Edited by admin on Sat Dec 16 19:50:34 GMT 2023
PRIMARY
CAS
71989-26-9
Created by admin on Sat Dec 16 19:50:34 GMT 2023 , Edited by admin on Sat Dec 16 19:50:34 GMT 2023
PRIMARY
FDA UNII
N8M8CCC7RN
Created by admin on Sat Dec 16 19:50:34 GMT 2023 , Edited by admin on Sat Dec 16 19:50:34 GMT 2023
PRIMARY
Related Record Type Details
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