52010-89-6

Basic information

• Product Name: Benzaldehyde, 2,5-dihydroxy-4-methyl-
• CAS NO: 52010-89-6
• Molecular Formula: C8H8O3
• Molecular Weight: 152.15
• Mol File: 52010-89-6.mol
• Article Data: 4

Chemical Properties

• CAS DataBase Reference: Benzaldehyde, 2,5-dihydroxy-4-methyl-(CAS DataBase Reference)
• NIST Chemistry Reference: Benzaldehyde, 2,5-dihydroxy-4-methyl-(52010-89-6)
• EPA Substance Registry System: Benzaldehyde, 2,5-dihydroxy-4-methyl-(52010-89-6)

Safety Data

• Hazardous Substances Data: 52010-89-6(Hazardous Substances Data)

Upstream product

• 698-27-1 4-methylsalicylaldehyde 
• 4925-88-6 2,5-dimethoxy-4-methylbenzaldehyde 
• 97088-24-9 1,4-dibromo-2,5-bis(methoxymethoxy)benzene 
• 14753-51-6 2,5-dibromohydroquinone 
• 681473-22-3 2,5-bis(methoxymethoxy)-4-bromotoluene 
• 40931-05-3 2,5-Bis(methoxymethoxy)-4-methyl-benzaldehyd 
• 24599-58-4 2,5-dimethoxy toluene 
• 100-97-0 hexamethylenetetramine 
• 95-71-6 2-methylbenzene-1,4-diol 

Downstream Products

• 4925-88-6 2,5-dimethoxy-4-methylbenzaldehyde 
• 939019-26-8 2,5-dihydroxy-4-methyl-benzyl alcohol 

Relevant articles and documents

A Total Synthesis of Paeoveitol

A four-step total synthesis of paeoveitol (1), a recently disclosed norditerpene natural product from Paeonia vetchii, is reported. This highly concise synthetic route was guided by biosynthetic considerations and enabled by an unusual intermolecular orth

Evaluation of HIV-1 inhibition by stereoisomers and analogues of the sesquiterpenoid hydroquinone peyssonol A

Peyssonol A, a brominated natural product with documented anti-HIV-1 activity, was synthesized racemically along with 6 isomers and 15 truncated analogues and synthetic precursors. These compounds were screened in a cell-based assay against a recombinant