2179-22-8

Basic information

• Product Name: Benzaldehyde, 2,5-dihydroxy-3-methoxy-
• CAS NO: 2179-22-8
• Molecular Formula: C8H8O4
• Molecular Weight: 168.149
• Mol File: 2179-22-8.mol
• Article Data: 4

Chemical Properties

• CAS DataBase Reference: Benzaldehyde, 2,5-dihydroxy-3-methoxy-(CAS DataBase Reference)
• NIST Chemistry Reference: Benzaldehyde, 2,5-dihydroxy-3-methoxy-(2179-22-8)
• EPA Substance Registry System: Benzaldehyde, 2,5-dihydroxy-3-methoxy-(2179-22-8)

Safety Data

• Hazardous Substances Data: 2179-22-8(Hazardous Substances Data)

Upstream product

• 148-53-8 3-methoxy-2-hydroxybenzaldehyde 
• 623-11-0 1-methyl-4-nitrosobenzene 
• 60582-31-2 2-Dimethoxymethyl-6-methoxy-p-benzochinon 
• 139209-92-0 2-Iodo-6-methoxy-benzene-1,4-diol 
• 4460-86-0 asaraldehyde 

Downstream Products

• 5556-84-3 2,3,5-trimethoxy-benzaldehyde 
• 110361-77-8 methyl 2,3,5-trimethoxybenzoate 
• 36873-96-8 2,3,5-trimethoxybenzoic acid 
• 292824-24-9 5-methoxy-3,6-dioxo-cyclohexa-1,4-dienecarbaldehyde 
• 138223-08-2 2,5-diethoxy-3-methoxybenzaldehyde 

Relevant articles and documents

Quinone approaches toward the synthesis of aflatoxin B2

equation presented Quinones bearing electron-withdrawing groups can serve as useful precursors to furobenzofuran ring systems through their reaction with 2,3-dihydrofuran. Formal racemic and stereoselective syntheses of the fungal metabolite aflatoxin Bs

Studies on Quinones. VII(1). Synthesis of Some Benzothiophene-4,7-diones

The synthesis of methyl 4,7-dihydro-4,7-dioxobenzothiophene-2-carboxylate (20) based on the reaction of methyl mercaptoacetate with activated 1,4-benzoquinones is described.Methyl 4,7-dihydro-4,7-dioxo-5-hydroxybenzothiophene-2-carboxylate (24) and its corresponding methyl ether 26 were obtained through a Thiele-Winter acetoxylation on 20.On the basis of the properties of methyl 4,7-dihydro-4,7-dioxo-6-methoxybenzothiophene-2-carboxylate (21) obtained from 2,4,5-trimethoxybenzaldehyde (32), the structures of the products 24 and 26 are proposed.