83324-59-8

Usage

Uses

3-chloro-4,6-dihydroxy-2-methylbenzaldehyde is a lichen/fungal metabolite.

Upstream product

• 504-15-4 orcinol 
• 7149-90-8 2,4-dimethoxy-6-methyl-benzaldehyde 
• 4179-19-5 1,3-dimethoxy-5-methylbenzene 
• 878479-97-1 3-chloro-4,6-dimethoxy-2-methylbenzaldehyde 
• 3446-05-7 4-chloro-5-methylbenzene-1,3-diol 
• 487-69-4 2,4-dihydroxy-6-methylbenzaldehyde 

Downstream Products

• 112990-33-7 3-chloro-4,6-bis-methoxycarbonyloxy-2-methyl-benzaldehyde 
• 83324-48-5 3-chloro-5-[(2E)-3,7-dimethylocta-2,6-dien-1-yl]-4,6-dihydroxy-2-methylbenzaldehyde 
• 93741-07-2 (+/-)-(E,E)-3-chloro-5-<7-(6,6-dimethyl-1,4,7-trioxaspiro<4.4>non-8-yl)-3-methyl-2,6-octadienyl>-4,6-dihydroxy-2-methylbenzaldehyde 
• 91854-87-4 3-chloro-4,6-dihydroxy-2-methyl-5-decane)-2,4-pentadienyl>benzaldehyde 
• 98066-13-8 3-Chloro-5-[(2E,6Z)-7-(6,6-dimethyl-1,4,7-trioxa-spiro[4.4]non-8-yl)-3-methyl-octa-2,6-dienyl]-4,6-dihydroxy-2-methyl-benzaldehyde 
• 878480-12-7 2-chloro-4-formyl-5-hydroxy-3-methylphenyl acetate 
• 878480-10-5 3-chloro-6-hydroxy-4-methoxymethoxy-2-methyl-benzaldehyde 
• 86832-77-1 dl-5-chloro-2,4-dihydroxy-6-methyl-3-[(2E,6E)-3-methyl-7-(3,3-dimethyl-4-oxo-2-oxacyclopentyl)-2,6-octadienyl]benzaldehyde 
• 188607-94-5 4-chloro-6-(5-chloro-naphthalen-2-ylmethyl)-2-formyl-5-hydroxy-3-methyl-phenol 
• 1374767-37-9 (2E,6E)-8-(3-chloro-5-formyl-2,6-dihydroxy-4-methylphenyl)-3,6-dimethyl-2,6-octadienyl pivalate 
• 1374767-19-7 3-chloro-4,6-dihydroxy-2-methyl-5-[(2E,6E,8E)-3,7,11,11-tetramethyl-10-o xo-2,6,8-dodecatrienyl]benzaldehyde 
• 1374767-20-0 3-chloro-4,6-dihydroxy-2-methyl-5-(2E,6E)-(8-methoxy-3,7,11,11-tetramethyl-10-oxo-2,6-dodecadienyl)benzaldehyde 
• 1374767-45-9 3-chloro-4,6-dihydroxy-5-[(E)-7-methoxy-3,7-dimethyl-2-octenyl]-2-methylbenzaldehyde 
• 1374767-39-1 3-chloro-4,6-dihydroxy-5-(2-octynyl)-2-methylbenzaldehyde 

Relevant academic research and scientific papers

COMPOUNDS FOR USE AS INHIBITORS OF ALTERNATIVE OXIDASE OR CYTOCHROME BC1 COMPLEX

The invention provides compounds for use in inhibiting a microbial alternative oxidase (AOX) and/or cytochrome bc1 complex. The invention extends to the use of such inhibitors in agrochemicals and in pharmaceuticals, for treating microbial infe

COMPOUNDS FOR USE AS INHIBITORS OF ALTERNATIVE OXIDASE OR CYTOCHROME BC1 COMPLEX

The invention provides compounds for use in inhibiting a microbial alternative oxidase (AOX) and/or cytochrome bc1 complex. The invention extends to the use of such inhibitors in agrochemicals and in pharmaceuticals, for treating microbial infe

Synthetic study for two 2H-chromenic acids, 8-chlorocannabiorcichromenic acid and mycochromenic acid

Two 2H-chromenes having a fully substituted benzene ring, 8-chlorocannabioreichromene (1) and mycochromenic acid (2), were synthesized by a condensation of salicylaldehydes with isopropylidenemalonate or the thermal cyclization of corresponding propargyl ethers.

New approach for two chromene carboxylic acids having a fully substituted benzene ring

Two chromene carboxylic acids having a fully substituted benzene ring, 8-chlorocannabiorcichromenic acid (1) and myco-chromenic acid (2), were synthesized via thermal cyclization of the corresponding four substituted phenyl propargyl ethers. Two chromene

A CONVENIENT SYNTHESIS OF (+/-) ASCOCHLORIN

A convergent total synthesis of (+/-) ascochlorin is described.

Total Syntheses of Fungal Metabolites and Functionalized Furanones

Simple, efficient syntheses of the fungal metabolites colletochlorin D and (+/-)-ascofuranone and one of its stereoisomers are described.Our investigations of functionalized furanones also enabled us to develop a nine-step (22percent overall yield) synthe

A GENERAL SYNTHETIC METHOD FOR PRENYLATED PHENOLS OF MICROBIAL ORIGIN

Prenylated phenols with a fully substituted benzene ring, such as colletochlorins A and B, were synthesized by first prenylating 1,5-dimethoxy-3-methyl-1,4-cyclohexadiene and then effecting the aromatization of the prenylated product.

SYNTHESIS OF COLLETOCHLORIN D

An efficient three-step synthesis of Colletochlorin D from orcinol has been achieved.