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Merck
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重要文件

557749

Sigma-Aldrich

N-Boc-5-溴吲哚

97%

同義詞:

5-溴吲哚-1-羧酸叔丁酯

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About This Item

經驗公式(希爾表示法):
C13H14BrNO2
CAS號碼:
分子量::
296.16
MDL號碼:
分類程式碼代碼:
12352100
PubChem物質ID:
NACRES:
NA.22
暫時無法取得訂價和供貨情況

化驗

97%

形狀

solid

mp

56-57 °C (lit.)

官能基

bromo

SMILES 字串

CC(C)(C)OC(=O)n1ccc2cc(Br)ccc12

InChI

1S/C13H14BrNO2/c1-13(2,3)17-12(16)15-7-6-9-8-10(14)4-5-11(9)15/h4-8H,1-3H3

InChI 密鑰

PBWDRTGTQIXVBR-UHFFFAOYSA-N

一般說明

N-Boc-5-bromoindole can undergo Sonogashira coupling reaction with N,N-diisopropylprop-2-ynylamine to afford the corresponding propargylic diisopropylamine.[1] N-Boc-5-bromoindole is formed as an intermediate during the synthesis of 2-(5-substituted-1H-indol-3-yl)-N-hydroxyacetamide derivatives.[2]

象形圖

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訊號詞

Warning

危險聲明

危險分類

Eye Irrit. 2 - Skin Irrit. 2 - STOT SE 3

標靶器官

Respiratory system

儲存類別代碼

11 - Combustible Solids

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

dust mask type N95 (US), Eyeshields, Gloves


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分析證明 (COA)

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Hiroyuki Nakamura et al.
The Journal of organic chemistry, 70(6), 2357-2360 (2005-03-12)
[reaction: see text] Propargylic diisopropylamines containing heterocycles, which were prepared readily from heterocyclic bromides and propargyldiisopropylamine by the Sonogashira coupling reaction, underwent the allene transformation reaction in the presence of Pd(2)(dba)(3).CHCl(3) catalyst (2.5 mol %) and 1,2-bis[bis(pentafluorophenyl)phosphino]ethane (10 mol %)
Sylvain Petit et al.
ChemMedChem, 4(2), 261-275 (2008-12-05)
The lead compound 5-bromoindolyl-3-acetohydroxamic acid (10) was recently identified as a potent inhibitor of bacterial peptide deformylases (PDFs). The synthesis and associated activities of new variants were investigated at position 5 to optimize the fit at the S1' subsite and

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