711950
(S)-3-(Boc-氨基)-5-己烯酸
98%
别名:
Boc-(S)-3-氨基-5-己烯酸
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关于此项目
经验公式（希尔记法）:
C11H19NO4
化学文摘社编号:
分子量:
229.27
UNSPSC Code:
12352108
NACRES:
NA.22
PubChem Substance ID:
MDL number:
Beilstein/REAXYS Number:
9127734
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.
signalword
Warning
hcodes
Hazard Classifications
Acute Tox. 4 Oral - Eye Irrit. 2 - Skin Irrit. 2 - STOT SE 3
target_organs
Respiratory system
存储类别
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
法规信息
新产品
此项目有
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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