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About This Item
线性分子式:
(CH3)3CC6H4CO2CH3
CAS号:
分子量:
192.25
EC 号:
MDL编号:
UNSPSC代码:
12352100
PubChem化学物质编号:
NACRES:
NA.22
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方案
99%
表单
liquid
折射率
n20/D 1.51 (lit.)
沸点
122-124 °C/9 mmHg (lit.)
密度
0.995 g/mL at 25 °C (lit.)
官能团
ester
SMILES字符串
COC(=O)c1ccc(cc1)C(C)(C)C
InChI
1S/C12H16O2/c1-12(2,3)10-7-5-9(6-8-10)11(13)14-4/h5-8H,1-4H3
InChI key
UPIJOAFHOIWPLT-UHFFFAOYSA-N
一般描述
Methyl 4-tert-butylbenzoate undergoes Claisen condensation reaction with 4-methoxyacetophenone to give avobenzone, an ingredient of sunscreen products.
应用
Methyl 4-tert-butylbenzoate was used in the synthesis of tris(4-tert-butylphenyl)methyl chloride.
警示用语：
Warning
危险分类
Acute Tox. 4 Dermal - Acute Tox. 4 Inhalation - Acute Tox. 4 Oral
储存分类代码
10 - Combustible liquids
WGK
WGK 3
闪点(°F)
270.5 °F
闪点(°C)
132.5 °C
个人防护装备
Eyeshields, Gloves
法规信息
新产品
Guoqing Zhang et al.
Journal of the American Chemical Society, 132(7), 2160-2162 (2010-01-30)
Difluoroboron avobenzone (BF(2)AVB), a simple boron complex of a commercial sunscreen product, exhibits morphology-dependent emission and mechanochromic luminescence in the solid state. When scratched, smeared, or even gently touched, the emission color of BF(2)AVB films is significantly red-shifted under UV
The tris (4- tert-butylphenyl) methyl group: a bulky substituant for effective regioselective difunctionalisation of cyclomaltohexaose.
Armspach D and Matt D.
Carbohydrate Research, 310(1), 129-133 (1998)
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