<生产厂家价格>

对氟苄胺

对氟苄胺用途

【用途一】
用作医药、农药中间体
【用途二】
抗过敏药物阿司咪唑，镇痛药Flupirine的中间体。

对氟苄胺名称

[ CAS 号 ]:
140-75-0

[ 中文名 ]:
对氟苄胺

[ 英文名 ]:
4-Fluorobenzylamine

[中文别名 ]:

[英文别名 ]:

(4-Fluorophenyl)methylamine
1-(4-Fluorophenyl)methanamine
(4-Fluorophenyl)methanamine
Benzenemethanamine, 4-fluoro-
MFCD00008120
Benzylamine, p-fluoro-
EINECS 205-430-4
p-Fluorobenzyl amine
Z1R DF

对氟苄胺物理化学性质

[ 密度 ]:
1.1±0.1 g/cm3

[ 沸点 ]:
184.3±15.0 °C at 760 mmHg

[ 分子式 ]:
C₇H₈FN

[ 分子量 ]:
125.144

[ 闪点 ]:
66.7±0.0 °C

[ 精确质量 ]:
125.064079

[ PSA ]:
26.02000

[ LogP ]:
1.14

[ 外观性状 ]:
透明无色液体

[ 蒸汽压 ]:
0.7±0.4 mmHg at 25°C

[ 折射率 ]:
1.523

[ 储存条件 ]:
2~8℃

对氟苄胺MSDS

对氟苄胺安全信息

[ 符号 ]:

GHS05

[ 信号词 ]:
Danger

[ 危害声明 ]:
H314

[ 警示性声明 ]:
P280-P305 + P351 + P338-P310

[ 个人防护装备 ]:
Faceshields;full-face respirator (US);Gloves;Goggles;multi-purpose combination respirator cartridge (US);type ABEK (EN14387) respirator filter

[ 危害码 (欧洲) ]:
C:Corrosive

[ 风险声明 (欧洲) ]:
R34

[ 安全声明 (欧洲) ]:
S26-S27-S36/37/39-S45-S36/39

[ 危险品运输编码 ]:
UN 2735 8/PG 2

[ WGK德国 ]:
3

[ 包装等级 ]:
III

[ 危险类别 ]:
8

[ 海关编码 ]:
2921499090

对氟苄胺合成路线

对氟苄胺上下游产品

对氟苄胺上游产品

对氟苄胺下游产品

对氟苄胺制备

在100ml反应瓶中加入N-（4-氟苯甲基）邻苯二甲酰亚胺 25.5g (0.1mol)和25ml无水乙醇,再加入80%水合肼溶液 6.3g (0.1mol),加热回流 0.5g 。加入过量的盐酸使析出的白色沉淀分解，冷却后加入适量的水搅拌，抽滤。滤液用NaOH溶液中和，用乙醚萃取，乙醚萃取液干燥后蒸除乙醚，减压蒸馏，收集44 -46 ℃ （67kPa）馏分，得对氟苄胺 7.1g ，收率56.5%。

对氟苄胺海关

[ 海关编码 ]: 2921499090

[ 中文概述 ]:
2921499090 其他芳香单胺及衍生物及它们的盐. 增值税率:17.0% 退税率:9.0% 监管条件:无最惠国关税:6.5% 普通关税:30.0%

[ 申报要素 ]: 品名, 成分含量, 用途

[ Summary ]:
2921499090 other aromatic monoamines and their derivatives; salts thereof VAT:17.0% Tax rebate rate:9.0% Supervision conditions:none MFN tariff:6.5% General tariff:30.0%

对氟苄胺文献

New efficient substrates for semicarbazide-sensitive amine oxidase/VAP-1 enzyme: analysis by SARs and computational docking.

J. Med. Chem. 49 , 6197-208, (2006)

Structure activity relationships for semicarbazide-sensitive amine oxidase/vascular adhesion protein-1 (SSAO/VAP-1) were studied using a library of arylalkylamine substrates, with the aim of contribut...

Fully automated synthesis of 4-[18F]fluorobenzylamine based on borohydride/NiCl2 reduction.

Nucl. Med. Biol. 40(3) , 430-6, (2013)

4-[(18)F]Fluorobenzylamine ([(18)F]FBA) is an important building block for the synthesis of (18)F-labeled compounds. Synthesis of [(18)F]FBA usually involves application of strong reducing agents like...

New lipophilic 3-hydroxy-4-pyridinonate iron(III) complexes: synthesis and EXAFS structural characterisation.

Dalton Trans. (10) , 1313-21, (2006)

New tris-iron(III) chelates of 3-hydroxy-4-pyridinone ligands derived from maltol (3-hydroxy-2-methyl-4-pyrone) or ethylmaltol (2-ethyl-3-hydroxy-4-pyrone), including a variety of N-aryl (phenyl, 4'-t...

更多文献