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Merck
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重要文件

90303

Sigma-Aldrich

4-(Boc-氨基)丁基溴

technical, ≥90% (AT)

同義詞:

N-(4-溴丁基)氨基甲酸叔丁酯

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About This Item

線性公式:
Br(CH2)4NHCO2C(CH3)3
CAS號碼:
分子量::
252.15
MDL號碼:
分類程式碼代碼:
12352200
PubChem物質ID:
NACRES:
NA.22
暫時無法取得訂價和供貨情況

等級

technical

品質等級

化驗

≥90% (AT)

形狀

liquid

反應適用性

reagent type: cross-linking reagent

雜質

~5% 1-boc-pyrrolidine

官能基

Boc
amine
bromo

儲存溫度

2-8°C

SMILES 字串

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)

InChI 密鑰

GKGFAEREWWZBKY-UHFFFAOYSA-N

應用

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.[1]
  • For the synthesis of various aloperine derivatives with potential application as anti-HIV agents.[2]
  • For the modification of 4,5,6,7-tetrabromobenzotriazole (TBB) derivatives to generate improved CK2 inhibitors.[3]

其他說明

合成天然产物和生物活性化合物的结构单元。[4][5]

象形圖

Corrosion

訊號詞

Danger

危險聲明

危險分類

Eye Dam. 1

儲存類別代碼

10 - Combustible liquids

水污染物質分類(WGK)

WGK 3

閃點(°F)

Not applicable

閃點(°C)

Not applicable

個人防護裝備

Eyeshields, Gloves, type ABEK (EN14387) respirator filter


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分析證明 (COA)

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存取文件庫

Structure Optimization of Aloperine Derivatives as HIV-1 Entry Inhibitors.
Dang Z, et al.
ACS Medicinal Chemistry Letters, 8(11), 1199-1203 (2017)
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)
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)
D.L. Selwood et al.
Journal of Medicinal Chemistry, 4, 78-78 (2001)
H. Ina et al.
The Journal of Organic Chemistry, 61, 1023 -1023 (1995)

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