所有图片(1)
About This Item
经验公式（希尔记法）:
C10H20N2O2
CAS号:
分子量:
200.28
Beilstein:
8905233
MDL编号:
UNSPSC代码:
12352005
PubChem化学物质编号:
NACRES:
NA.22
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方案
≥96.5% (GC)
96.5-103.5% (NT)
97%
表单
solid
光学纯度
enantiomeric excess: ≥97.5% (GC)
储存温度
2-8°C
SMILES字符串
CC(C)(C)OC(=O)N1CCC[C@H]1CN
InChI
1S/C10H20N2O2/c1-10(2,3)14-9(13)12-6-4-5-8(12)7-11/h8H,4-7,11H2,1-3H3/t8-/m0/s1
InChI key
SOGXYCNKQQJEED-QMMMGPOBSA-N
应用
(S)-2-(Aminomethyl)-1-Boc-pyrrolidine can be used as a building block to synthesize:
- Imidazo[1,2-b]pyridazine derivatives as potent IKKβ inhibitors.
- 1,2-dicarba-closo-dodecaborane (o-carborane) and 1,7-dicarba-closo-dodecaborane (m-carborane) derivatives as potential D2 receptor antagonists.
- Pyrrolidine based Merrifield resin as a chiral organocatalyst for the asymmetric Michael addition reaction of ketones with nitrostyrenes.
包装
Bottomless glass bottle. Contents are inside inserted fused cone.
警示用语：
Danger
危险声明
危险分类
Acute Tox. 4 Oral - Skin Corr. 1B
储存分类代码
8A - Combustible corrosive hazardous materials
WGK
WGK 3
闪点(°F)
Not applicable
闪点(°C)
Not applicable
个人防护装备
Eyeshields, Faceshields, Gloves, type P3 (EN 143) respirator cartridges
法规信息
新产品
从最新的版本中选择一种：
分析证书(COA)
Lot/Batch Number
Discovery of imidazo [1, 2-b] pyridazines as IKK? inhibitors. Part 3: Exploration of effective compounds in arthritis models
Shimizu H, et al.
Bioorganic & Medicinal Chemistry Letters, 21(15), 4550-4555 (2011)
Synthesis of D2 receptor ligand analogs incorporating one dicarba-closo-dodecaborane unit
Vazquez, N, et al.
Tetrahedron Letters, 52(5), 615-618 (2011)
Recyclable Merrifield resin-supported organocatalysts containing pyrrolidine unit through A3-coupling reaction linkage for asymmetric Michael addition
Liu J, et al.
Chirality, 22(4), 432-441 (2010)
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