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Merck
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文件

337110

Sigma-Aldrich

2-氟-4-甲基苯胺

99%

别名:

2-氟对甲苯胺

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About This Item

线性分子式:
FC6H3(CH3)NH2
CAS号:
452-80-2
分子量:
125.14
MDL號碼:
MFCD00040975
分類程式碼代碼:
12352100
PubChem物質ID:
24860458
NACRES:
NA.22

化驗

99%

形狀

liquid

折射率

n20/D 1.533 (lit.)

bp

70-71 °C/7 mmHg (lit.)

密度

1.108 g/mL at 25 °C (lit.)

SMILES 字串

Cc1ccc(N)c(F)c1

InChI

1S/C7H8FN/c1-5-2-3-7(9)6(8)4-5/h2-4H,9H2,1H3

InChI 密鑰

ZQEXBVHABAJPHJ-UHFFFAOYSA-N

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一般說明

Rat liver microsomal metabolism of 2-fluoro-4-methylaniline was studied by HPLC.

應用

2-Fluoro-4-methylaniline was used in the preparation of 6-chloro-5-fluoroindole via Leimgruber-Batcho reaction. It was also used in the preparation of an (S)-amino alcohol, 2-amino-3-(2-fluoro-4-methylphenyl)-propan-1-ol.

象形圖

Skull and crossbones
GHS06

訊號詞

Danger

危險分類

Acute Tox. 3 Oral - Eye Irrit. 2 - Skin Irrit. 2 - STOT SE 3

標靶器官

Respiratory system

儲存類別代碼

6.1C - Combustible acute toxic Cat.3 / toxic compounds or compounds which causing chronic effects

水污染物質分類（WGK）

WGK 3

閃點（°F）

174.2 °F - closed cup

閃點（°C）

79 °C - closed cup

個人防護裝備

Eyeshields, Faceshields, Gloves, type ABEK (EN14387) respirator filter

分析证书(COA)

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Sharon T Marino et al.
Molecules (Basel, Switzerland), 9(6), 405-426 (2007-11-17)
In the past decade there has been a significant growth in the sales of pharmaceutical drugs worldwide, but more importantly there has been a dramatic growth in the sales of single enantiomer drugs. The pharmaceutical industry has a rising demand
S Boeren et al.
Xenobiotica; the fate of foreign compounds in biological systems, 22(12), 1403-1423 (1992-12-01)
1. Rat liver microsomal metabolism of 2-fluoro-, 2-chloro- and 2-bromo-4-methylaniline was investigated using h.p.l.c. Metabolites identified include products from side-chain C-hydroxylation (benzyl alcohols and benzaldehydes) and N-hydroxylation (hydroxylamines and nitroso derivatives). Aromatic ring hydroxylation was not a major reaction pathway.
J M Bentley et al.
Bioorganic & medicinal chemistry letters, 14(9), 2367-2370 (2004-04-15)
A series of 1-(1-indolinyl)-2-propylamines was synthesised and evaluated as 5-HT(2C) receptor agonists for the treatment of obesity. The general methods of synthesis of the precursor indoles are described. The functional efficacy and radioligand binding data for all of the compounds

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