21405-60-7

Basic information

• Product Name: Propanedioic acid, [(4-methylphenyl)methyl]-
• CAS NO: 21405-60-7
• Molecular Formula: C11H12O4
• Molecular Weight: 208.214
• Mol File: 21405-60-7.mol
• Article Data: 3

Chemical Properties

• CAS DataBase Reference: Propanedioic acid, [(4-methylphenyl)methyl]-(CAS DataBase Reference)
• NIST Chemistry Reference: Propanedioic acid, [(4-methylphenyl)methyl]-(21405-60-7)
• EPA Substance Registry System: Propanedioic acid, [(4-methylphenyl)methyl]-(21405-60-7)

Safety Data

• Hazardous Substances Data: 21405-60-7(Hazardous Substances Data)

Upstream product

• 5553-86-6 (4-methylbenzyl)malononitrile 
• 104-81-4 4-Methylbenzyl bromide 
• 108-88-3 toluene 
• 104-82-5 4-Methylbenzyl chloride 
• 6619-58-5 diethyl 4-methylbenzylmalonate 

Downstream Products

• 1505-50-6 3-(4-Methylphenyl)propanoic acid 
• 240801-32-5 vinyl 3-(4-methylphenyl)propanoate 
• 107673-39-2 2-(4-Methyl-benzyl)-acrylic acid 
• 111510-56-6 Thiobenzoic acid S-(2-chlorocarbonyl-3-p-tolyl-propyl) ester 
• 111510-45-3 2-Benzoylsulfanylmethyl-3-p-tolyl-propionic acid 
• 107673-28-9 (R)-3-Ethylsulfanyl-2-(2-mercaptomethyl-3-p-tolyl-propionylamino)-propionic acid 
• 107688-59-5 (R)-2-(2-Benzoylsulfanylmethyl-3-p-tolyl-propionylamino)-3-ethylsulfanyl-propionic acid 

Relevant articles and documents

Synthesis and insecticidal activity of mesoionic pyrido[1,2-α]pyrimidinone derivatives containing a neonicotinoid moiety

Mesoionic pyrido[1,2-α]pyrimidinone derivatives containing a neonicotinoid moiety were designed, synthesized, and evaluated for their insecticidal activity. Some of the title compounds showed remarkable insecticidal properties against Aphis craccivora. Compound I13 exhibited satisfactory insecticidal activity against A. craccivora. Meanwhile, label-free proteomics analysis of compound I13 treatment identified a total of 821 proteins. Of these, 35 proteins were up-regulated, whereas 108 proteins were down-regulated. Differential expressions of these proteins reflected a change in cellular structure and metabolism.

Sulfur-containing acylamino acids. II. Syntheses and angiotensin I converting enzyme-inhibitory activities of N-mercaptoalkanoyl-S-ethyl-L-cysteine

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