N2-Fmoc-N6-BOC-L-lysine

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 Search

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 UTC 2023` Edited by `admin` on `Sat Dec 16 19:50:34 UTC 2023`
Record UNII	N8M8CCC7RN
Record Status	`Validated (UNII)`
Record Version

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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 UTC 2023 , Edited by admin on Sat Dec 16 19:50:34 UTC 2023

PRIMARY

EPA CompTox

DTXSID901316712

Created by admin on Sat Dec 16 19:50:34 UTC 2023 , Edited by admin on Sat Dec 16 19:50:34 UTC 2023

PRIMARY

CAS

71989-26-9

Created by admin on Sat Dec 16 19:50:34 UTC 2023 , Edited by admin on Sat Dec 16 19:50:34 UTC 2023

PRIMARY

FDA UNII

N8M8CCC7RN

Created by admin on Sat Dec 16 19:50:34 UTC 2023 , Edited by admin on Sat Dec 16 19:50:34 UTC 2023

PRIMARY

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