推荐产品
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
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
其他客户在看
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
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
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
The International journal of biochemistry, 14(7), 649-653 (1982-01-01)
1. The thiobarbituric acid (TBA) reaction, widely applied to the detection of autoxidation in polyunsaturated fatty acids, can be used to measure free-radical damage to amino acids, carbohydrates and nucleic acids. 2. In all of these systems malondialdehyde (MDA) is
Archives of biochemistry and biophysics, 387(2), 173-179 (2001-05-24)
The indole moeity is present in many substances of biological occurrence. Its metabolism, in most cases, involves an oxidative pathway. This study reports the oxidation of a series of indole derivatives, including several of biological origin, catalyzed by horseradish peroxidase
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