90303
4-(Boc-氨基)丁基溴
technical, ≥90% (AT)
别名:
N-(4-溴丁基)氨基甲酸叔丁酯
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关于此项目
线性分子式:
Br(CH2)4NHCO2C(CH3)3
化学文摘社编号:
分子量:
252.15
NACRES:
NA.22
PubChem Substance ID:
UNSPSC Code:
12352200
MDL number:
Assay:
≥90% (AT)
Form:
liquid
InChI key
GKGFAEREWWZBKY-UHFFFAOYSA-N
SMILES string
BrCCCCNC(OC(C)(C)C)=O
InChI
1S/C9H18BrNO2/c1-9(2,3)13-8(12)11-7-5-4-6-10/h4-7H2,1-3H3,(H,11,12)
grade
technical
assay
≥90% (AT)
form
liquid
reaction suitability
reagent type: cross-linking reagent
impurities
~5% 1-boc-pyrrolidine
functional group
Boc, amine, bromo
storage temp.
2-8°C
Quality Level
Application
4-(Boc-amino)butyl bromide can be used:
- For the synthesis of N-Boc-aminoalkoxyphenyl derivatives, precursor to pharmacophore elements for the treatment of glaucoma.
- For the synthesis of various aloperine derivatives with potential application as anti-HIV agents.
- For the modification of 4,5,6,7-tetrabromobenzotriazole (TBB) derivatives to generate improved CK2 inhibitors.
Other Notes
合成天然产物和生物活性化合物的结构单元。
signalword
Danger
hcodes
Hazard Classifications
Eye Dam. 1
存储类别
10 - Combustible liquids
wgk
WGK 3
flash_point_f
Not applicable
flash_point_c
Not applicable
ppe
Eyeshields, Gloves, type ABEK (EN14387) respirator filter
法规信息
新产品
此项目有
Identification of bivalent ligands with melatonin receptor agonist and fatty acid amide hydrolase (FAAH) inhibitory activity that exhibit ocular hypotensive effect in the rabbit.
Spadoni G, et al.
Journal of medicinal chemistry, 61(17), 7902-7916 (2018)
Synthesis, biological activity and structural study of new benzotriazole-based protein kinase CK2 inhibitors.
Swider R, et al.
Royal Society of Chemistry Advances, 5(89), 72482-72494 (2015)
H. Ina et al.
The Journal of Organic Chemistry, 61, 1023 -1023 (1995)
Structure Optimization of Aloperine Derivatives as HIV-1 Entry Inhibitors.
Dang Z, et al.
ACS Medicinal Chemistry Letters, 8(11), 1199-1203 (2017)
D.L. Selwood et al.
Journal of Medicinal Chemistry, 4, 78-78 (2001)
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