131379-19-6

Basic information

• Product Name: Benzoic acid, 4-(1-oxopentyl)-, ethyl ester
• CAS NO: 131379-19-6
• Molecular Formula: C14H18O3
• Molecular Weight: 234.295
• Mol File: 131379-19-6.mol
• Article Data: 3

Chemical Properties

• CAS DataBase Reference: Benzoic acid, 4-(1-oxopentyl)-, ethyl ester(CAS DataBase Reference)
• NIST Chemistry Reference: Benzoic acid, 4-(1-oxopentyl)-, ethyl ester(131379-19-6)
• EPA Substance Registry System: Benzoic acid, 4-(1-oxopentyl)-, ethyl ester(131379-19-6)

Safety Data

• Hazardous Substances Data: 131379-19-6(Hazardous Substances Data)

Upstream product

• 638-29-9 n-valeryl chloride 
• 131379-15-2 (4-(ethoxycarbonyl)phenyl)zinc(ll) bromide 
• 51934-41-9 4-iodobenzoic acid ethyl ester 

Downstream Products

• 360-34-9 1,1,1-trifluoro-2-hexanone 
• 636-09-9 diethyl terephthalate 
• 934494-94-7 tert-butyl (2E)-2-{1-[4-(ethoxycarbonyl)phenyl]pentylidene}hydrazine-carboxylate 

Relevant articles and documents

Pyrazole derivatives, compositions containing such compounds and methods of use

Pyrazoles having a naphthyl group attached are disclosed. The compounds are useful for treating type 2 diabetes and related conditions. Pharmaceutical compositions and methods of treatment are also included.

The Direct Formation of Functionalized Alkyl(aryl)zinc Halides by Oxidative Addition of Highly Reactive Zinc with Organic Halides and Their Reactions with Acid Chlorides, α,β-Unsaturated Ketones, and Allylic, Aryl, and Vinyl Halides

Highly reactive zinc, prepared by the lithium naphthalenide reduction of ZnCl2, readily undergoes oxidative addition to alkyl, aryl, and vinyl halides under mild conditions to generate the corresponding organozinc compounds in excellent yields.Significantly, the reaction will tolerate a spectrum of functional groups on the organic halides.Accordingly, this approach can now be used to prepare a wide variety of highly functionalized organozinc compounds.In the presence of Cu(I) salts, the organozinc compounds cross-couple with acid chlorides, conjugatively add to α,β-unsaturated ketones, and regioselectively undergo SN2' substitution reactions with allylic halides.They also cross-couple with aryl or vinyl halides with Pd(0) catalysts.