863676-70-4

Basic information

• Product Name: 3-chloro-2-hydroxy-6-methylbenzoic acid ethyl ester
• Synonyms: 3-chloro-2-hydroxy-6-methylbenzoic acid ethyl ester
• CAS NO: 863676-70-4
• Molecular Weight: 214.649
• Mol File: 863676-70-4.mol
• Article Data: 3

Chemical Properties

• CAS DataBase Reference: 3-chloro-2-hydroxy-6-methylbenzoic acid ethyl ester(CAS DataBase Reference)
• NIST Chemistry Reference: 3-chloro-2-hydroxy-6-methylbenzoic acid ethyl ester(863676-70-4)
• EPA Substance Registry System: 3-chloro-2-hydroxy-6-methylbenzoic acid ethyl ester(863676-70-4)

Safety Data

• Hazardous Substances Data: 863676-70-4(Hazardous Substances Data)

Upstream product

• 4652-27-1 4-methoxy-3-buten-2-one 
• 1031694-93-5 4-chloro-1-ethoxy-1,3-bis-(trimethylsilyloxy)buta-1,3-diene 
• 3419-32-7 ethyl 5-methyl-3-oxocyclohexene-4-carboxylate 
• 6555-40-4 ethyl 2-hydroxy-6-methylbenzoate 

Downstream Products

• 863676-76-0 ethyl 3-chloro-2-methoxy-6-dibromomethylbenzoate 
• 863676-75-9 ethyl 3-chloro-2-methoxy-6-methylbenzoate 

Relevant articles and documents

Synthesis of functionalized salicylates by formal [3+3] cyclocondensation of 1,3-bis(silyloxy)buta-1,3-dienes with 3-alkoxy-2-en-1-ones

The formal [3+3] cyclization of 1,3-bis(silyloxy)buta-1,3-dienes with 1-aryl-3-ethoxyprop-2-en-1-ones, available by Heck reaction of benzoyl chlorides with ethyl vinyl ether, afforded a variety of 6-arylsalicylates. The reaction of the products with conce

Total synthesis of BE-23254, a chlorinated angucycline antibiotic

The first synthesis of BE-23254, an unusual angucycline antibiotic, is reported. It involves regioselective condensation of naphthalenone 4 and chlorine-containing isobenzofuranone 16 as the key step.