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Merck

422541

Sigma-Aldrich

5-甲基水杨酸乙酯

98%

别名:

2-羟基-5-甲基苯甲酸乙酯

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About This Item

线性分子式:
CH3C6H3(OH)CO2C2H5
CAS号:
分子量:
180.20
EC號碼:
MDL號碼:
分類程式碼代碼:
12352100
PubChem物質ID:
NACRES:
NA.22

化驗

98%

折射率

n20/D 1.522 (lit.)

bp

251 °C (lit.)

密度

1.103 g/mL at 25 °C (lit.)

SMILES 字串

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 密鑰

ZGYXABNSOOACGL-UHFFFAOYSA-N

一般說明

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.

象形圖

FlameExclamation mark

訊號詞

Warning

危險分類

Acute Tox. 4 Dermal - Acute Tox. 4 Inhalation - Acute Tox. 4 Oral - Eye Irrit. 2 - Flam. Liq. 3 - Skin Irrit. 2 - STOT SE 3

標靶器官

Respiratory system

儲存類別代碼

3 - Flammable liquids

水污染物質分類(WGK)

WGK 3

閃點(°F)

98.6 °F - closed cup

閃點(°C)

37 °C - closed cup

個人防護裝備

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


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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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