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Merck
CN

457396

Sigma-Aldrich

4-氟吲哚

97%

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About This Item

经验公式(希尔记法):
C8H6FN
CAS号:
分子量:
135.14
MDL编号:
UNSPSC代码:
12352100
PubChem化学物质编号:
NACRES:
NA.22

质量水平

方案

97%

沸点

90 °C/0.4 mmHg (lit.)

mp

30-32 °C (lit.)

官能团

fluoro

SMILES字符串

Fc1cccc2[nH]ccc12

InChI

1S/C8H6FN/c9-7-2-1-3-8-6(7)4-5-10-8/h1-5,10H

InChI key

ZWKIJOPJWWZLDI-UHFFFAOYSA-N

应用

  • Reactant for preparation of tryptophan dioxygenase inhibitors pyridyl-ethenyl-indoles as potential anticancer immunomodulators
  • Reactant for preparation of antifungal agents
  • Reactant for preparation of Sodium-Dependent Glucose Co-transporter 2 (SGLT2) Inhibitors for the Management of Hyperglycemia in Diabetes
  • Reactant for preparation of Potent Selective Serotonin Reuptake Inhibitors
  • Reactant for preparation of Inhibitors of HIV-1 attachment
  • Reactant for preparation of monoamine reuptake inhibitors
  • Reactant for preparation of histone deacetylase (HDAC) inhibitors
  • Reactant for preparation of inhibitors of proliferation of human breast cancer cells

象形图

Exclamation mark

警示用语:

Warning

危险声明

危险分类

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

靶器官

Respiratory system

储存分类代码

11 - Combustible Solids

WGK

WGK 3

个人防护装备

dust mask type N95 (US), Eyeshields, Gloves

法规信息

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分析证书(COA)

Lot/Batch Number

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访问文档库

(Erratum)
Journal of Medicinal Chemistry, 2442-2442 null
Synthesis of (L)-4-Fluorotryptophan.
Konas DW, et al.
Synthetic Communications, 42(1), 144-152 (2012)
Journal of the Chemical Society. Perkin Transactions 1, 1765-1765 (1994)
J L Malleron et al.
Journal of medicinal chemistry, 36(9), 1194-1202 (1993-04-30)
A series of new indole derivatives (2-28) has been prepared in the search for novel 5-HT uptake inhibitors. These compounds were obtained by the condensation of N-(chloroalkyl) naphthalenesultam derivatives with the appropriate amine in presence of a base, at reflux
4-Fluoroindole and Derivatives.
Bentov M, et al.
Israel J. Chem., 2(1), 25-28 (1964)

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