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384038

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

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关于此项目

线性分子式:
(CH3)3CC6H4CHO
化学文摘社编号:
939-97-9
分子量:
162.23
UNSPSC Code:
12352100
NACRES:
NA.22
PubChem Substance ID:
24863644
EC Number:
213-367-9
Beilstein/REAXYS Number:
1906461
MDL number:
MFCD00035742
Assay:
97%
Form:
liquid
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Quality Level

200

assay

97%

form

liquid

refractive index

n20/D 1.53 (lit.)

bp

130 °C/25 mmHg (lit.)

density

0.97 g/mL at 25 °C (lit.)

SMILES string

[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

General description

4-叔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- 叔 -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- 叔 丁基苯胺和 4- 叔 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。

Application

4- 叔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)。

signalword

Danger

Hazard Classifications

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

存储类别

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

wgk

WGK 3

flash_point_f

213.8 °F - closed cup

flash_point_c

101 °C - closed cup

ppe

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
BCCL9981
BCCK6616
BCCJ2946
BCCG6961
BCCF1717

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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
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全球贸易项目编号

货号GTIN
384038-25ML04061831965285
384038-5ML04061836684990