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4-butyl-5-pentyl-2-((2S,3R,4R,5S,6R)-3,4,5-trihydroxy-6-(hydroxymethyl)tetrahydro-2H-pyran-2-yl)cyclohex-2-enone is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

1268482-84-3

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1268482-84-3 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 1268482-84-3 includes 10 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 7 digits, 1,2,6,8,4,8 and 2 respectively; the second part has 2 digits, 8 and 4 respectively.
Calculate Digit Verification of CAS Registry Number 1268482-84:
(9*1)+(8*2)+(7*6)+(6*8)+(5*4)+(4*8)+(3*2)+(2*8)+(1*4)=193
193 % 10 = 3
So 1268482-84-3 is a valid CAS Registry Number.

1268482-84-3Relevant academic research and scientific papers

AMPHIPHILIC COMPOSITIONS AND METHODS FOR PREPARING AND USING SAME

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Page/Page column 46, (2011/06/11)

The invention relates to amphiphilic C-glycoside derivatives, to methods of using them and to processes for synthesizing them. Specifically, the invention relates to novel cyclic and linear enone-glycolipids and cyclic ketone-glycolipids.

Linear and cyclic C-glycosides as surfactants

Foley, Patrick M.,Phimphachanh, Anthony,Beach, Evan S.,Zimmerman, Julie B.,Anastas, Paul T.

experimental part, p. 321 - 325 (2011/04/17)

Carbohydrate-based surfactants have long been of interest due to their desirable performance properties and their potential to be derived from renewable feedstocks. Although most carbohydrate based surfactants utilize an O-glycosidic linkage, recent advances in carbohydrate C-C bond formation allows for the facile synthesis of new classes of carbohydrate-based surfactants on a C-glycosidic linkage. Herein is described an approach that can generate a wide variety of C-glycoside surfactants in moderate to very good yield by treating the nonulose C-glycoside intermediate first described by Lubineau et al. with pyrrolidine in the presence of an alkyl aldehyde. Depending on the stoichiometry and reaction conditions, this chemistry will result in either a linear enone C-glycoside, or a cyclohexenone C-glycoside, both of which demonstrate interesting surfactant properties. Further, the linear enone series can be photochemically modified or reacted with other alkyl aldehydes to generate additional analogs.

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