跳转至内容
Merck
CN

384038

Sigma-Aldrich

4-叔丁基苯甲醛

97%

别名:

4-(1,1-二甲基乙基)苯甲醛, 对叔丁基苯甲醛

登录查看公司和协议定价


About This Item

线性分子式:
(CH3)3CC6H4CHO
CAS号:
分子量:
162.23
Beilstein:
1906461
EC 号:
MDL编号:
UNSPSC代码:
12352100
PubChem化学物质编号:
NACRES:
NA.22

质量水平

方案

97%

表单

liquid

折射率

n20/D 1.53 (lit.)

沸点

130 °C/25 mmHg (lit.)

密度

0.97 g/mL at 25 °C (lit.)

SMILES字符串

[H]C(=O)c1ccc(cc1)C(C)(C)C

InChI

1S/C11H14O/c1-11(2,3)10-6-4-9(8-12)5-7-10/h4-8H,1-3H3

InChI key

OTXINXDGSUFPNU-UHFFFAOYSA-N

正在寻找类似产品? 访问 产品对比指南

相关类别

一般描述

4-丁基苯甲醛是合成医药、染料、香料和香料的重要中间体。据报告,它是在冰醋酸中用过氧化氢部分氧化 4--丁基甲苯过程中形成的,由溴离子与乙酸钴 (II) 或乙酸铈 (III) 结合催化。在基体辅助激光解吸电离 (MALDI) 室中进行了 4- 丁基苯胺和 4- 丁基苯甲醛在乙醇中的 Schiff 碱反应,对生成的亚胺进行了实时检测。

应用

4-丁基苯甲醛适用于动力学研究,以评价 4-取代苯甲醛抑制蘑菇酪氨酸酶的动力学常数 (KI)。

警示用语:

Danger

危险分类

Acute Tox. 3 Oral - Aquatic Acute 1 - Repr. 2 - Skin Sens. 1

储存分类代码

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

WGK

WGK 3

闪点(°F)

213.8 °F - closed cup

闪点(°C)

101 °C - closed cup

个人防护装备

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


历史批次信息供参考:

分析证书(COA)

Lot/Batch Number

没有发现合适的版本?

如果您需要特殊版本,可通过批号或批次号查找具体证书。

已有该产品?

在文件库中查找您最近购买产品的文档。

访问文档库

Leon G A van de Water et al.
Chemistry (Weinheim an der Bergstrasse, Germany), 13(28), 8037-8044 (2007-07-12)
The partial oxidation of 4-tert-butyltoluene to 4-tert-butylbenzaldehyde by hydrogen peroxide in glacial acetic acid, catalyzed by bromide ions in combination with cobalt(II) acetate or cerium(III) acetate, has been studied in detail. Based on the observed differences in reaction rates and
Monica Brivio et al.
Lab on a chip, 5(4), 378-381 (2005-03-26)
The integration of a monitoring port along the microfluidic path of a MALDI-chip integrated device is described. Optimization of the microreactor design allows longer reaction and measuring times. The Schiff base reaction between 4-tert-butylaniline (1) and 4-tert-butylbenzaldehyde (2) in ethanol
M Jiménez et al.
Journal of agricultural and food chemistry, 49(8), 4060-4063 (2001-08-22)
A kinetic study of the inhibition of mushroom tyrosinase by 4-substituted benzaldehydes showed that these compounds behave as classical competitive inhibitors, inhibiting the oxidation of L-3,4-dihydroxyphenylalanine (L-DOPA) by mushroom tyrosinase (o-diphenolase activity). The kinetic parameter (K(I)) characterizing this inhibition was
Chao-Bin Xue et al.
Bioorganic & medicinal chemistry, 15(5), 2006-2015 (2007-01-30)
Phenoloxidase (PO), also known as tyrosinase, is a key enzyme in insect development, responsible for catalyzing the hydroxylation of tyrosine into o-diphenols and the oxidation of o-diphenols into o-quinones. Inhibition of PO may provide a basis for novel environmentally friendly

我们的科学家团队拥有各种研究领域经验,包括生命科学、材料科学、化学合成、色谱、分析及许多其他领域.

联系技术服务部门