14982
Boc-β3-Homopro-OH
≥98.0% (TLC)
别名:
(S)-2-(1-叔丁氧羰基-2-吡咯烷基)乙酸, Boc-L-β3-高脯氨酸
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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:
12352202
NACRES:
NA.22
PubChem Substance ID:
MDL number:
Beilstein/REAXYS Number:
478306
assay
≥98.0% (TLC)
reaction suitability
reaction type: Boc solid-phase peptide synthesis
application(s)
peptide synthesis
SMILES string
CC(C)(C)OC(=O)N1CCC[C@H]1CC(O)=O
InChI
1S/C11H19NO4/c1-11(2,3)16-10(15)12-6-4-5-8(12)7-9(13)14/h8H,4-7H2,1-3H3,(H,13,14)/t8-/m0/s1
InChI key
GDWKIRLZWQQMIE-QMMMGPOBSA-N
Other Notes
千里光生物碱类的结构单元；合成精氨酸加压素的新型类似物。
存储类别
11 - Combustible Solids
wgk
WGK 3
flash_point_f
Not applicable
flash_point_c
Not applicable
ppe
Eyeshields, Gloves, type N95 (US)
法规信息
新产品
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Proline analogues are promising candidates for tuning the biological, pharmaceutical, or physicochemical properties of naturally occuring, as well as de novo designed, linear, and, cyclic peptides.
D.W. Knight et al.
Journal of the Chemical Society. Perkin Transactions 1, 1615-1615 (1991)
K. Bankowski et al.
Collection of Czechoslovak Chemical Communications, 54, 2795-2795 (1989)
全球贸易项目编号
| 货号 | GTIN |
|---|---|
| B103268-25ML | 04061836693480 |
| B103268-5ML | 04061836693497 |
| 14982-1G | 04061826100592 |