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(4R,5R)-5-<(benzyloxy)methyl>-4-methyltetrahydrofuran-2(3H)-one is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

85428-27-9

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85428-27-9 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 85428-27-9 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 8,5,4,2 and 8 respectively; the second part has 2 digits, 2 and 7 respectively.
Calculate Digit Verification of CAS Registry Number 85428-27:
(7*8)+(6*5)+(5*4)+(4*2)+(3*8)+(2*2)+(1*7)=149
149 % 10 = 9
So 85428-27-9 is a valid CAS Registry Number.

85428-27-9Relevant academic research and scientific papers

FORMATION AND REACTIONS OF TRICHLORO-γ-LACTONES

Takano, Seiichi,Nishizawa, Shin'ichi,Akiyama, Masashi,Ogasawara, Kunio

, p. 1779 - 1788 (2007/10/02)

The allyl trichloroacetates, (6) and (7), have been converted into the trichloro-γ-lactones, (8) and (9), by cuprous chloride.On dechlorination using tri-n-butyltin hydride, regioselective reaction has occurred initially at α position to convert the trich

L'ELDANOLIDE, PHEROMONE DES GLANDES ALAIRES DE LA PYRALE DE LA CANNE A SUCRE, ELDANA SACCHARINA (WLK.): STRUCTURE ET SYNTHESE DE SES DEUX ENANTIOMERES

Vigneron, J. P.,Meric, R.,Larcheveque, M.,Debal, A.,Lallemand, J. Y.,et al.

, p. 3521 - 3530 (2007/10/02)

The isolation and structure determination of eldanolide, the wing gland pheromone of the male African Sugar Cane Borer, Eldana saccharina (Wlk.) is described.The absolute configuration was determined as (3S, 4R) by comparison of the CD spectra of the natural pheromone with both synthetic enantiomers.

ABSOLUTE CONFIGURATION OF ELDANOLIDE, THE WING GLAND PHEROMONE OF THE MALE AFRICAN CANE BORER, ELDANA SACCHARINA (WLK.) SYNTHESES OF ITS (+) AND (-) ENANTIOMERS.

Vigneron, J. P.,Meric, R.,Larcheveque, M.,Debal, A.,Kunesch, G.,et al.

, p. 5051 - 5054 (2007/10/02)

Eldanolide 1, a novel terpenoid lactone pheromone, was shown to have (3S,4R) configuration by synthesis of both enantiomers and comparison of their CD with the natural pheromone.

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