Sign In to View Organizational & Contract Pricing.
Select a Size
Change View
About This Item
Empirical Formula (Hill Notation):
C11H19NO4
CAS Number:
Molecular Weight:
229.27
UNSPSC Code:
12352108
NACRES:
NA.22
PubChem Substance ID:
MDL number:
Beilstein/REAXYS Number:
9127734
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
SMILES string
CC(C)(C)OC(=O)N[C@@H](CC=C)CC(O)=O
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
InChI key
RFHPQLCVYMBPRF-QMMMGPOBSA-N
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.
signalword
Warning
hcodes
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
新产品
This item has
Choose from one of the most recent versions:
Already Own This Product?
Find documentation for the products that you have recently purchased in the Document Library.
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)
Global Trade Item Number
| SKU | GTIN |
|---|---|
| 711950-250MG | 04061832719757 |
