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Merck
CN

222720

Sigma-Aldrich

对氟肉桂酸

99%

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线性分子式:
FC6H4CH=CHCO2H
CAS号:
分子量:
166.15
EC 号:
MDL编号:
UNSPSC代码:
12352100
PubChem化学物质编号:
NACRES:
NA.22

质量水平

检测方案

99%

形式

powder

mp

209-210 °C (lit.)

SMILES字符串

OC(=O)\C=C\c1ccc(F)cc1

InChI

1S/C9H7FO2/c10-8-4-1-7(2-5-8)3-6-9(11)12/h1-6H,(H,11,12)/b6-3+

InChI key

ISMMYAZSUSYVQG-ZZXKWVIFSA-N

一般描述

The shock loading of 4-fluorocinnamic acid (4-FCA) was treated using a rotating biological contactor (RBC).

应用

4-Fluorocinnamic acid was used in growth medium for the Arthrobacter sp. strain G1.

象形图

Skull and crossbones

警示用语:

Danger

危险分类

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

靶器官

Respiratory system

WGK

WGK 3

闪点(°F)

Not applicable

闪点(°C)

Not applicable

个人防护装备

Eyeshields, Gloves, type N95 (US)

法规信息

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Catarina L Amorim et al.
Bioresource technology, 144, 554-562 (2013-08-01)
A rotating biological contactor (RBC) was used to treat shock loadings of 4-fluorocinnamic acid (4-FCA). Intermittent 4-FCA shocks of 35 mg L(-1) were applied (ca. 3 months) with only limited mineralization occurring and accumulation of 4-fluorobenzoate (4-FBA) as an intermediate.
Syed A Hasan et al.
Biodegradation, 23(1), 117-125 (2011-07-06)
Arthrobacter sp. strain G1 is able to grow on 4-fluorocinnamic acid (4-FCA) as sole carbon source. The organism converts 4-FCA into 4-fluorobenzoic acid (4-FBA) and utilizes the two-carbon side-chain for growth with some formation of 4-fluoroacetophenone as a dead-end side
Ivana Perković et al.
European journal of medicinal chemistry, 187, 111927-111927 (2019-12-08)
Harmicines constitute novel hybrid compounds that combine two agents with reported antiplasmodial properties, namely β-carboline harmine and a cinnamic acid derivative (CAD). Cu(I) catalyzed azide-alkyne cycloaddition was employed for the preparation of three classes of hybrid molecules: N-harmicines 6a-i, O-harmicines
Marina Marinović et al.
Molecules (Basel, Switzerland), 25(19) (2020-09-27)
Harmicines represent hybrid compounds composed of β-carboline alkaloid harmine and cinnamic acid derivatives (CADs). In this paper we report the synthesis of amide-type harmicines and the evaluation of their biological activity. N-harmicines 5a-f and O-harmicines 6a-h were prepared by a

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