Welcome to LookChem.com Sign In|Join Free
  • or
2(3H)-Furanone, dihydro-5-methyl-3-(phenylmethyl)- is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

14557-92-7

Post Buying Request

14557-92-7 Suppliers

Recommended suppliers

  • Product
  • FOB Price
  • Min.Order
  • Supply Ability
  • Supplier
  • Contact Supplier

14557-92-7 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 14557-92-7 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 1,4,5,5 and 7 respectively; the second part has 2 digits, 9 and 2 respectively.
Calculate Digit Verification of CAS Registry Number 14557-92:
(7*1)+(6*4)+(5*5)+(4*5)+(3*7)+(2*9)+(1*2)=117
117 % 10 = 7
So 14557-92-7 is a valid CAS Registry Number.

14557-92-7Relevant academic research and scientific papers

New syntheses on the basis of ethyl 2-oxotetrahydrofuran-3-carboxylates

Kochikyan,Arutyunyan,Arutyunyan,Avetisyan

experimental part, p. 849 - 854 (2009/06/08)

Alkylation of 5-substituted ethyl 5-methyl-2-oxotetrahydrofuran-3- carboxylates with alkyl halides in the presence of sodium ethoxide gave the corresponding 3-alkyl derivatives which were converted into 3,5-substituted 5-methyl-N-(4-nitrophenyl)-2-oxotetr

Combined dealkoxycarbonylation and lactonisation of unsaturated malonates in ionic liquids

Oswald, Magalie F.,Parsons, Andrew F.,Yang, Wei,Bowden, Martin

, p. 8087 - 8089 (2007/10/03)

Heating unsaturated malonates with LiCl and water in [bmim][Br] or [bmim][BF4]/[bmim][Br] produces unsaturated esters or lactones, respectively.

Reaction of silyl ketene acetals with epoxides: A new method for the synthesis of γ-butanolides

Maslak, Veselin,Matovi?, Radomir,Sai?i?, Radomir N.

, p. 8957 - 8966 (2007/10/03)

Titanium tetrachloride promoted reaction of silyl ketene acetals with epoxides, followed by acidic work-up, affords butanolides in moderate/good yields. With epihalohydrins the reaction is regioselective and occurs at the less substituted end of the epoxide; the γ-haloalkyl-γ-butanolides thus obtained can be further transformed into various products. Graphical Abstract

CYCLODESHYDRATION DE DIOLS EN PRESENCE D'HMPT1

Diab, J.,Abou-Assali, M.,Gervais, C.,Anker, D.

, p. 1501 - 1502 (2007/10/02)

1,4 and 1,5-diols heated with 0.3 equivalent of HMPA undergo cyclodehydration leading to tetrahydrofurans and tetrahydropyrans.

Post a RFQ

Enter 15 to 2000 letters.Word count: 0 letters

Attach files(File Format: Jpeg, Jpg, Gif, Png, PDF, PPT, Zip, Rar,Word or Excel Maximum File Size: 3MB)

1 Customer Service

What can I do for you?
Get Best Price

Get Best Price for 14557-92-7