| Identification | Back Directory | [Name]
ETHYL 2-HYDROXY-5-METHYLBENZOATE | [CAS]
34265-58-2 | [Synonyms]
RARECHEM AL BI 0811
ETHYL 5-METHYLSALICYLATE
Ethyl 5-methylsalicylate 98%
2,5-Cresotic acid ethyl ester
ETHYL 2-HYDROXY-5-METHYLBENZOATE
Ethyl 6-hydroxy-3-methylbenzoate
5-Methylsalicylic acid ethyl ester
2-hydroxy-5-methyl-benzoicaciethylester
Benzoicacid,2-hydroxy-5-methyl-,ethylester
2-hydroxy-5-methyl-benzoic acid ethyl ester | [EINECS(EC#)]
251-903-3 | [Molecular Formula]
C10H12O3 | [MDL Number]
MFCD00192161 | [MOL File]
34265-58-2.mol | [Molecular Weight]
180.2 |
| Chemical Properties | Back Directory | [Melting point ]
2℃ | [Boiling point ]
251 °C(lit.) | [density ]
1.103 g/mL at 25 °C(lit.) | [refractive index ]
n20/D 1.522(lit.) | [Fp ]
98 °F | [storage temp. ]
RT, stored under nitrogen | [pka]
10.23±0.18(Predicted) | [Appearance]
Light yellow to yellow Liquid | [InChI]
1S/C10H12O3/c1-3-13-10(12)8-6-7(2)4-5-9(8)11/h4-6,11H,3H2,1-2H3 | [InChIKey]
ZGYXABNSOOACGL-UHFFFAOYSA-N | [SMILES]
CCOC(=O)c1cc(C)ccc1O | [EPA Substance Registry System]
Benzoic acid, 2-hydroxy-5-methyl-, ethyl ester (34265-58-2) |
| Safety Data | Back Directory | [Hazard Codes ]
Xn | [Risk Statements ]
10-20/21/22-36/37/38 | [Safety Statements ]
16-26-36 | [RIDADR ]
UN 3272 3/PG 3 | [WGK Germany ]
3 | [TSCA ]
TSCA listed | [Storage Class]
3 - Flammable liquids | [Hazard Classifications]
Acute Tox. 4 Dermal
Acute Tox. 4 Inhalation
Acute Tox. 4 Oral
Eye Irrit. 2
Flam. Liq. 3
Skin Irrit. 2
STOT SE 3 |
| Hazard Information | Back Directory | [Uses]
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. | [General Description]
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. |
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| Company Name: |
Energy Chemical
|
| Tel: |
021-021-58432009 400-005-6266 |
| Website: |
http://www.energy-chemical.com |
| Company Name: |
Sigma-Aldrich
|
| Tel: |
021-61415566 800-8193336 |
| Website: |
https://www.sigmaaldrich.cn |
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