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heptakis(2,6-di-O-pentyl)-β-cyclodextrin hepta(3-phenylcarbamate) is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

143205-27-0

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143205-27-0 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 143205-27-0 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,4,3,2,0 and 5 respectively; the second part has 2 digits, 2 and 7 respectively.
Calculate Digit Verification of CAS Registry Number 143205-27:
(8*1)+(7*4)+(6*3)+(5*2)+(4*0)+(3*5)+(2*2)+(1*7)=90
90 % 10 = 0
So 143205-27-0 is a valid CAS Registry Number.

143205-27-0Downstream Products

143205-27-0Relevant academic research and scientific papers

Carbamate Derivatives of β-Cyclodextrin as Chiral Stationary Phases for Metal Capillary Gas Chromatography

Takeichi, Tsutomu,Shimura, Sigeru,Toriyama, Hisashi,Takayama, Yuzi,Morikawa, Masami

, p. 1069 - 1072 (1992)

Three kinds of novel chiral stationary phases for capillary gas chromatography, heptakis(2,6-di-O-pentyl)-β-cyclodextrin hepta(3-n-propyl, 3-isopropyl, and 3-phenylcarbamate), were prepared.Metal capillary columns coated with the stationary phases showed impressive enantioseparation toward many kinds of racemic compounds.

Characterization of the cyclomalto-hexaose and -heptaose derivatives by the reductive-cleavaeg method

Mischnick-Luebbecke, Petra,Krebber, Ralph

, p. 197 - 202 (2007/10/02)

The substitution patterns of cyclomalto-hexaose and -heptaose derivatives carrying alkyl, acyl, and carbamoyl substituents have been investigated by the reductive-cleavage method.The modified cyclomalto-hexaoses or -heptaoses were treated with triethylsilane and trimethylsilyl trifluoromethanesulfonate to give the corresponding 1,5- and 1,4-anhydroglucitol derivatives that were acetylated or, in the case of acetyl derivatives, trifluoroacetylated and analysed by g.l.c.-m.s.For the alkylated compounds, minute amounts of products formed by under- or over-alkylation, or of isomeric components, could be detected.Partial reduction of the acyloxy groups to alkyloxy groups and cleavage of acyl substituents were observed.Carbamoyl substituents were stable under the conditions of reductive cleavage.

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