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经验公式(希尔记法):
C11H22N2O2
化学文摘社编号:
分子量:
214.30
PubChem Substance ID:
UNSPSC Code:
12352100
Beilstein/REAXYS Number:
7023643
MDL number:
产品名称
(±)-3-(Boc-氨基甲基)哌啶, ≥98.0% (TLC)
SMILES string
CC(C)(C)OC(=O)NCC1CCCNC1
InChI
1S/C11H22N2O2/c1-11(2,3)15-10(14)13-8-9-5-4-6-12-7-9/h9,12H,4-8H2,1-3H3,(H,13,14)
InChI key
KHPQHXGYYXYTDN-UHFFFAOYSA-N
assay
≥98.0% (TLC)
form
solid
storage temp.
2-8°C
Application
Reagent for:
Preparation of Tylophorine analogs
Enzymatic acylation
Preparation of Tylophorine analogs
Enzymatic acylation
signalword
Danger
hcodes
Hazard Classifications
Skin Corr. 1B
存储类别
8A - Combustible corrosive hazardous materials
wgk
WGK 3
flash_point_f
Not applicable
flash_point_c
Not applicable
ppe
Eyeshields, Faceshields, Gloves, type P3 (EN 143) respirator cartridges
法规信息
新产品
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商品
Mono-Boc-protected diamines are versatile building blocks for chemical synthesis. Their production is a lot more challenging than the simple reaction scheme might imply, because the Boc-anhydride reagent cannot differentiate between the two identical amino moieties in the substrate.
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