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Merck
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重要文件

M51407

Sigma-Aldrich

2-甲基吲哚

98%

同義詞:

NSC 7514

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About This Item

經驗公式(希爾表示法):
C9H9N
CAS號碼:
分子量::
131.17
Beilstein:
109781
EC號碼:
MDL號碼:
分類程式碼代碼:
12352100
PubChem物質ID:
NACRES:
NA.22

品質等級

化驗

98%

bp

273 °C (lit.)

mp

57-59 °C (lit.)

SMILES 字串

Cc1cc2ccccc2[nH]1

InChI

1S/C9H9N/c1-7-6-8-4-2-3-5-9(8)10-7/h2-6,10H,1H3

InChI 密鑰

BHNHHSOHWZKFOX-UHFFFAOYSA-N

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應用

反应物用于:
  • 碘催化 Markovnikov 加成反应区域选择性合成氧代吡咯烷类似物
  • Friedel-Crafts 烷基化反应
  • 抗肿瘤免疫调节剂色氨酸双加氧酶抑制剂的制备
  • 植物生长抑制剂的制备
  • Michael 加成反应
  • 环氧化酶-1 (COX-1)/环氧化酶-2 (COX-2) 抑制剂的合成

象形圖

Exclamation mark

訊號詞

Warning

危險聲明

危險分類

Acute Tox. 4 Oral

儲存類別代碼

11 - Combustible Solids

水污染物質分類(WGK)

WGK 3

閃點(°F)

285.8 °F

閃點(°C)

141 °C

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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T Bhattacharya et al.
Spectrochimica acta. Part A, Molecular and biomolecular spectroscopy, 60(8-9), 1957-1966 (2004-07-14)
Electrochemical measurements by cyclic voltammetry predict the possibility of occurrence of photoinduced electron-transfer (PET) reactions between the ground state of 2-phenylindole (2PI) (electron donor) and the excited singlet of 9-cyanoanthracene (9CNA) molecule acting as an electron acceptor. However, 2PI should
N G Faleev et al.
Biochemistry and molecular biology international, 35(5), 1037-1040 (1995-04-01)
Tryptophanase was generally considered to be inactive towards tryptophan derivatives substituted at 2-position of the indole ring. We have shown that cells containing tryptophanase catalyze the formation of 2-methyl-L-tryptophan from 2-methylindole and L-serine, and from 2-methylindole, pyruvate and ammonium ion.
Emma L Harry et al.
The Analyst, 136(8), 1728-1732 (2011-02-26)
The potential of ion mobility (IM) spectrometry in combination with mass spectrometry (MS) for real-time reaction monitoring is reported. The combined IM-MS approach using electrospray ionization affords gas-phase analyte characterization based on both mass-to-charge (m/z) ratio and gas-phase ion mobility
T Misra et al.
Spectrochimica acta. Part A, Molecular and biomolecular spectroscopy, 58(8), 1631-1641 (2002-08-09)
By using steady state and time-resolved (laser flash photolysis and single photon counting) spectroscopic techniques the quenching of the lowest excited singlet (S1) state of 9-cyanoanthracene (9CNA) by the donors (quenchers) 2-methylindole (2MI) and 2-methylindoline (2MIN) in solvents of different
[2-Methylindoles substituted in the 1st, 3d and 5th positions and the diffuse neuroendocrine APUD system].
K S Shadurskiĭ et al.
Farmakologiia i toksikologiia, 46(2), 115-120 (1983-03-01)

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