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Merck
CN

711950

(S)-3-(Boc-amino)-5-hexenoic acid

98%

Synonym(s):

Boc-(S)-3-amino-5-hexenoic acid

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About This Item

Empirical Formula (Hill Notation):
C11H19NO4
CAS Number:
270263-03-1
Molecular Weight:
229.27
UNSPSC Code:
12352108
NACRES:
NA.22
PubChem Substance ID:
329763101
MDL number:
MFCD01861087
Beilstein/REAXYS Number:
9127734

Key Documents

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InChI

1S/C11H19NO4/c1-5-6-8(7-9(13)14)12-10(15)16-11(2,3)4/h5,8H,1,6-7H2,2-4H3,(H,12,15)(H,13,14)/t8-/m0/s1

SMILES string

CC(C)(C)OC(=O)N[C@@H](CC=C)CC(O)=O

InChI key

RFHPQLCVYMBPRF-QMMMGPOBSA-N

assay

≥97.5% (HPLC), 98%

form

lumps

optical activity

[α]/D +20±1°, c = 1 in ethanol

optical purity

enantiomeric excess: ≥99.0%

application(s)

peptide synthesis

storage temp.

2-8°C

Application

(S)-3-(Boc-amino)-5-hexenoic acid can be used as a reactant for the preparation of lactam bridged peptide mimics by peptide coupling and olefin metathesis.

Packaging

Bottomless glass bottle. Contents are inside inserted fused cone.

pictograms

Exclamation mark
GHS07

signalword

Warning

Hazard Classifications

Acute Tox. 4 Oral - Eye Irrit. 2 - Skin Irrit. 2 - STOT SE 3

target_organs

Respiratory system

Storage Class

11 - Combustible Solids

wgk

WGK 3

flash_point_f

Not applicable

flash_point_c

Not applicable

ppe

dust mask type N95 (US), Eyeshields, Faceshields, Gloves

Regulatory Information

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Certificates of Analysis (COA)

Lot/Batch Number
1411854V
1411854

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Short and efficient synthesis of homo-Freidinger lactams: an olefin metathesis approach towards conformationally restricted β-amino acid analogues
Hoffmann T and Gmeiner P
Synlett, 2002(06), 1014-1016 (2002)

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