16313-77-2

Usage

InChI:InChI=1/C10H12O2/c1-7-4-8(2)10(12-3)9(5-7)6-11/h4-6H,1-3H3

Upstream product

• 4885-02-3 Dichloromethyl methyl ether 
• 6738-23-4 2,4-dimethylanisole 
• 24623-61-8 3,5-dimethylsalicylaldehyde 
• 74-88-4 methyl iodide 
• 65001-66-3 2,4-dimethyl-6-propenyl-anisole 
• 122-51-0 orthoformic acid triethyl ester 
• 107153-65-1 1-(2-methoxy-3,5-dimethyl-phenyl)-propane-1,2-diol 

Downstream Products

• 106591-58-6 1-(2-methoxy-3,5-dimethyl-phenyl)-2-methyl-but-1-en-3-one 
• 60813-72-1 (Z)-1-(2-Methoxy-3,5-dimethyl-phenyl)-5-methyl-hexa-1,4-dien-3-one 
• 1196791-94-2 ethyl (E)-3-(2-methoxy-3,5-dimethylphenyl)acrylate 
• 16285-62-4 3-(2-methoxy-3,5-dimethylphenyl)prop-2-enoic acid 
• 16285-63-5 3-(2-methoxy-3,5-dimethylphenyl)propanic acid 
• 100611-94-7 3-(2-methoxy-3,5-dimethyl-phenyl)-2-methyl-acrylaldehyde 
• 21553-47-9 2-Methoxy-3,5-dimethylbenzoic acid 
• 101100-57-6 1-(2-methoxy-3,5-dimethyl-phenyl)-2-methyl-pent-3-en-1-ol 

Relevant academic research and scientific papers

Cockroach collective baiting material, cockroach collective attractant and cockroach exterminator (by machine translation)

The invention uses as a cockroach collective baiting material represented by general formula (I) - (III) of any of the compound or its salt, the solution comprising the cockroach collective pheromonal and cockroach collective pheromonal the cockroach coll

Total syntheses of all stereoisomers of phenatic acid B

(Chemical Equation Presented) The total syntheses of all stereoisomers of phenatic acid B and determination of their absolute configuration are described. The synthetic strategy is based on an efficient combination of the Sharpless asymmetric dihydroxylat

Tricyclic compounds, their production and use

A compound of the formula: wherein R1 is H or a substituent; m is 1-3; Ar is an aromatic group which may be substituted; X is a bond or a divalent straight-chain group having 1-6 atoms which may be substituted; Y is —S—, —O—, or —N(R2— (R2 is H or a substituent group), Z is —N= or —C(R3)= (R3 is H or a hydrocarbon group), ring A is a benzene ring; ring B is a 5- to 7-membered ring which may be substituted, or a salt thereof is useful for eliciting a prostaglandin I2 receptor agonistic effect.