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关于此项目
经验公式(希尔记法):
C9H18N2O2
化学文摘社编号:
分子量:
186.25
UNSPSC Code:
12352005
NACRES:
NA.22
PubChem Substance ID:
MDL number:
Beilstein/REAXYS Number:
5377813
Assay:
≥98.0% (TLC)
Form:
solid
assay
≥98.0% (TLC)
form
solid
optical activity
[α]/D -21.5±2.0°, c = 1 in ethanol
SMILES string
CC(C)(C)OC(=O)N[C@H]1CCNC1
InChI
1S/C9H18N2O2/c1-9(2,3)13-8(12)11-7-4-5-10-6-7/h7,10H,4-6H2,1-3H3,(H,11,12)/t7-/m0/s1
InChI key
DQQJBEAXSOOCPG-ZETCQYMHSA-N
Application
(S)-3-(Boc-amino)pyrrolidine can be used as a building block to prepare:
- 2,4,6-trisubstitued pyrido[3,4-d]pyrimidine derivatives as potent inhibitors against EGFR tyrosine kinase.
- Aminopyrrolidine scaffolds for asymmetric Morita−Baylis-Hillman reaction.
- N-benzyl-3-sulfonamidopyrrolidines as potent bacterial cell division inhibitors.
signalword
Warning
hcodes
Hazard Classifications
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, Gloves
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.
N-Benzyl-3-sulfonamidopyrrolidines as novel inhibitors of cell division in E. coli
Mukherjee S, et al.
Bioorganic & medicinal chemistry letters, 17(23), 6651-6655 (2007)
Chiral 3-aminopyrrolidines as a rigid diamino scaffold for organocatalysis and organometallic chemistry
Pouliquen M, et al.
Tetrahedron Asymmetry, 21(11-12), 1511-1521 (2010)
Synthesis and biological evaluation of irreversible EGFR tyrosine kinase inhibitors containing pyrido [3, 4-d] pyrimidine scaffold
Zhang H, et al.
Bioorganic & Medicinal Chemistry, 26(12), 3619-3633 (2018)
全球贸易项目编号
| 货号 | GTIN |
|---|---|
| 52927-5G-F | 04061832986326 |
| 52927-1G-F | 04061826129739 |
