103986-82-9

Basic information

• Product Name: methyl 3-acetyl-4-methoxybenzoate
• Synonyms: methyl 3-acetyl-4-methoxybenzoate
• CAS NO: 103986-82-9
• Molecular Weight: 208.214
• Mol File: 103986-82-9.mol
• Article Data: 5

Chemical Properties

• CAS DataBase Reference: methyl 3-acetyl-4-methoxybenzoate(CAS DataBase Reference)
• NIST Chemistry Reference: methyl 3-acetyl-4-methoxybenzoate(103986-82-9)
• EPA Substance Registry System: methyl 3-acetyl-4-methoxybenzoate(103986-82-9)

Safety Data

• Hazardous Substances Data: 103986-82-9(Hazardous Substances Data)

Upstream product

• 16357-40-7 3-acetyl-4-hydroxybenzoic acid 
• 67-56-1 methanol 
• 13235-60-4 4-methoxy-1,3-benzenedicarbonyl dichloride 
• 75-16-1 methylmagnesium bromide 
• 74-88-4 methyl iodide 

Downstream Products

• 1195945-07-3 3-(1,3-dihydroxy-3-m-tolyl-propyl)-4-methoxy-benzoic acid methyl ester 
• 1195945-06-2 4-methoxy-3-(2-m-tolyloxy-acetyl)-benzoic acid methyl ester 
• 1195945-08-4 4-methoxy-3-(3-m-tolyl-propyl)-benzoic acid methyl ester 
• 1357395-29-9 3-(3-hydroxy-3,7-dimethyloct-6-enoyl)-4-methoxybenzoic acid 
• 1357395-28-8 3-(1,3-dihydroxy-3,7-dimethyloct-6-en-1-yl)-4-methoxybenzoic acid 
• 1357395-27-7 methyl 3-(1,3-dihydroxy-3,7-dimethyloct-6-en-1-yl)-4-methoxybenzoate 
• 1357395-26-6 methyl 3-(3-hydroxy-3,7-dimethyloct-6-enoyl)-4-methoxybenzoate 
• 1195945-05-1 methyl 3-(2-bromoacetyl)-4-methoxybenzoate 
• 105401-95-4 3-isopropyl-4-methoxy-benzoic acid methyl ester 
• 882809-90-7 1-(2-methoxy-5-carboxymethylphenyl)-3-hydroxy-3-methyl-1-butanone 
• 246247-82-5 methyl 4-methoxy-3-(3-methyl-2-butenoyl)benzoate 
• 882809-86-1 1-(2-methoxy-5-carboxymethylphenyl)-1-trimethylsilyloxyethylene 
• 100117-39-3 3-isopropenyl-4-methoxy-benzoic acid methyl ester 

Relevant articles and documents

INDANE DERIVATIVES FOR USE IN THE TREATMENT OF BACTERIAL INFECTION

The invention relates to a compound which is an indane according to Formula (I), or a pharmaceutically acceptable salt thereof, wherein R1, R2, R3, R4, R5, R6, L, M, ?, n, p, and q are as defined herein. The compounds are useful in the treatment of antibacterial infection either as stand alone antibiotics, or in combination with further antibiotics.

Chalcone derivatives and drugs containing the same

PCT No. PCT/JP97/01652 Sec. 371 Date Nov. 17, 1998 Sec. 102(e) Date Nov. 17, 1998 PCT Filed May 16, 1997 PCT Pub. No. WO97/44306 PCT Pub. Date Nov. 27, 1997This invention relates to chalcone derivatives represented by the following formula (1): wherein A represents a phenyl group, a quinolyl group or the like, W represents a vinylene group or the like, and R1 to R5 each independently represent a carboxyl, cyano, alkyloxycarbonyl or like group, or salts of the chalcone derivatives, and also to drugs containing them as effective ingredients. These compounds have excellent cys-LT receptor antagonism, and are useful as antiallergic agents or the like.

Alkyliron and Alkylcobalt Reagents, VIII. - Alkyl-Iron(II) Compounds as Reagents and Catalysts for the Transformation of Acyl Chlorides into Ketones

Me2Fe, Bu2Fe, Me3FeLi, or Bu3FeLi - prepared in situ by reduction of FeCl3 to FeCl2 and subsequent alkylation with MeLi, MeMgBr, BuLi, or BuMgBr - are useful reagents for the conversion of acyl chlorides into ketones.The system (RMgX + catalytic amount of FeCl3) react like the FeII reagents with acyl chlorides to give ketones even at -65 deg C.Competition experiments with benzoyl chloride/2-methoxybenzoyl chloride show that the selectivity increases (competition constants Kk = 9.9, 10.7, 10.9, 15.0, ca. 110) in the sequence MeFeCl, Me2Fe, Me3Fe(MgBr), Me4Fe(MgBr)2, and catalytic system (MeMgBr + 2.5 mol percent FeCl3) (= 2, 3, 4, 5, and 40MeMgBr per 1 FeCl3, respectively).A new hypothesis on the nature of the active catalyst is discussed. Key Words: Organoiron compounds / Iron catalysts / Ketone synthesis