60241-75-0

Basic information

• Product Name: Benzoic acid, 2,3,6-trimethoxy-, methyl ester
• Synonyms: 2,3,6-Trimethoxybenzoesaeuremethylester;Methyl-2,3,6-trimethoxybenzoat;2,3,6-trimethoxy-benzoic acid methyl ester;Benzoic acid,2,3,6-trimethoxy-,methyl ester
• CAS NO: 60241-75-0
• Molecular Formula: C11H14O5
• Molecular Weight: 226.229
• Mol File: 60241-75-0.mol
• Article Data: 3

Chemical Properties

• Melting Point: 52-54 °C
• Boiling Point: 140-145 °C(Press: 0.02 Torr)
• Density: 1.134±0.06 g/cm3(Predicted)
• CAS DataBase Reference: Benzoic acid, 2,3,6-trimethoxy-, methyl ester(CAS DataBase Reference)
• NIST Chemistry Reference: Benzoic acid, 2,3,6-trimethoxy-, methyl ester(60241-75-0)
• EPA Substance Registry System: Benzoic acid, 2,3,6-trimethoxy-, methyl ester(60241-75-0)

Safety Data

• Hazardous Substances Data: 60241-75-0(Hazardous Substances Data)

Upstream product

• 135-77-3 1,2,4-trimethoxy-benzene 
• 79-22-1 methyl chloroformate 
• 60241-74-9 2,3,6-trimethoxybenzoic acid 
• 77-78-1 dimethyl sulfate 
• 67-56-1 methanol 

Downstream Products

• 25991-81-5 1,3-dihydroxy-7,8-dimethoxyxanthone 
• 114567-42-9 1,3-dihydroxy-5,8-dimethoxyxanthone 
• 156723-06-7 4-(1-methylethyl)-2,3,5-trimethoxyphenylmethyl alcohol 
• 60241-77-2 1,2,4-trimethoxy-3-(prop-1-en-2-yl)benzene 
• 60241-78-3 3-(1-methylethyl)-1,2,4-trimethoxybenzene 
• 866464-96-2 4-isopropyl-2,3,5-trimethoxybenzyl chloride 
• 866464-91-7 4-(1-methylethyl)-2,3,5-trimethoxybenzaldehyde 
• 60241-76-1 3-(1-methyl-1-hydroxyethyl)-1,2,4-trimethoxybenzene 
• 79817-85-9 2-Hydroxy-3,5,6-tribrom-1,4-benzochinon 
• 60241-74-9 2,3,6-trimethoxybenzoic acid 

Relevant articles and documents

Method for preparing 1,3,5,8-tetrahydroxy xanthone and 1,3,7,8-tetrahydroxy xanthone

The invention discloses a method for preparing 1,3,5,8-tetrahydroxy xanthone and 1,3,7,8-tetrahydroxy xanthone. The method comprises the following steps: by taking 1,2,4-trimetoxybenzene as an initialraw material, and adding n-butyllithium and a chloro-ca

Stereoselective syntheses of (±)-komaroviquinone and (±)-faveline methyl ether through intramolecular Heck reaction

An efficient, flexible, and stereoselective convergent route for constructing the trans-10-hydroxy-1,1-dimethyloctahydrodibenzo[a,d]cyclohepten- 7-ones (5a-c) was achieved via intramolecular Heck reaction. This strategy has been successfully implemented for the syntheses of (±)-komaroviquinone (3) through (±)-coulterone dimethyl ether (5c) and (±)-faveline methyl ether (1a).