672084
(S)-(氨甲基)-1-BOC-吡咯烷
97%
别名:
(R)-2-氨甲基-1-叔丁氧羰基吡咯烷, (S)-2-氨甲基吡咯烷-1-甲酸叔丁酯
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关于此项目
经验公式（希尔记法）:
C10H20N2O2
化学文摘社编号:
分子量:
200.28
UNSPSC Code:
12352005
NACRES:
NA.22
PubChem Substance ID:
MDL number:
Beilstein/REAXYS Number:
8905233
Assay:
≥96.5% (GC), 96.5-103.5% (NT), 97%
Form:
solid
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
SMILES string
CC(C)(C)OC(=O)N1CCC[C@H]1CN
InChI key
SOGXYCNKQQJEED-QMMMGPOBSA-N
assay
≥96.5% (GC), 96.5-103.5% (NT), 97%
form
solid
optical purity
enantiomeric excess: ≥97.5% (GC)
storage temp.
2-8°C
Application
(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.
Packaging
Bottomless glass bottle. Contents are inside inserted fused cone.
signalword
Danger
hcodes
Hazard Classifications
Acute Tox. 4 Oral - 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
此项目有
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)
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)
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