所有图片(1)
About This Item
线性分子式:
CH3C6H3(OH)CO2C2H5
CAS号:
分子量:
180.20
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
98%
折射率
n20/D 1.522 (lit.)
沸点
251 °C (lit.)
密度
1.103 g/mL at 25 °C (lit.)
官能团
ester
SMILES字符串
CCOC(=O)c1cc(C)ccc1O
InChI
1S/C10H12O3/c1-3-13-10(12)8-6-7(2)4-5-9(8)11/h4-6,11H,3H2,1-2H3
InChI key
ZGYXABNSOOACGL-UHFFFAOYSA-N
一般描述
Ethyl 5-methylsalicylate (ethyl 2-hydroxy-5-methylbenzoate) is a hydroxyl benzoate derivative. One of the methods reported for its synthesis is the esterification of p-cresotinic acid with absolute alcohol. It is formed as an intermediate during the synthesis of 2-propoxy-5-methylbenzoic acid. Ethyl 2-hydroxy-5-methylbenzoate has been isolated as a minor by product in the AlCl3 promoted reaction of 2-methyl furan with ethyl propiolate.
警示用语:
Warning
危险分类
Acute Tox. 4 Dermal - Acute Tox. 4 Inhalation - Acute Tox. 4 Oral - Eye Irrit. 2 - Flam. Liq. 3 - Skin Irrit. 2 - STOT SE 3
靶器官
Respiratory system
储存分类代码
3 - Flammable liquids
WGK
WGK 3
闪点(°F)
98.6 °F - closed cup
闪点(°C)
37 °C - closed cup
个人防护装备
Eyeshields, Faceshields, Gloves, type ABEK (EN14387) respirator filter
Synthesis of 2-Propoxy-5-Methylbenzoic Acid.
Brauer GM and Simon L.
Synthesis, 66(4), 313-315 (1962)
Influence of Lewis Acids on the Diels-Alder Reaction. IV. Reaction of 2-Methyl-and 2-Phenylfuran with Ethyl Propiolate.
McCulloch AW and McInnes AG.
Canadian Journal of Chemistry, 49(19), 3152-3157 (1971)
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