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(+)-1-O-benzyl-2,3,4,5,6-penta-O-acetyl-D-myo-inositol is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

38183-34-5

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38183-34-5 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 38183-34-5 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 3,8,1,8 and 3 respectively; the second part has 2 digits, 3 and 4 respectively.
Calculate Digit Verification of CAS Registry Number 38183-34:
(7*3)+(6*8)+(5*1)+(4*8)+(3*3)+(2*3)+(1*4)=125
125 % 10 = 5
So 38183-34-5 is a valid CAS Registry Number.

38183-34-5Relevant academic research and scientific papers

Design and synthesis of biotinylated inositol phosphates relevant to the biotin-avidin techniques

Anraku, Kensaku,Inoue, Teruhiko,Sugimoto, Kenji,Morii, Takashi,Mori, Yasuo,Okamoto, Yoshinari,Otsuka, Masami

supporting information; experimental part, p. 1822 - 1830 (2008/10/09)

Six bifunctional molecules containing biotin and various inositol phosphates were synthesized. These compounds were designed on the basis of X-ray structures of the complexes of d-myo-inositol 1,4,5-triphosphates (IP 3) and phospholipase C δ pleckstrin homology domain (PLCδ PH) considering the application to the biotin-avidin techniques. The building blocks of the inositol moiety were synthesized starting with optically resolved myo-inositol derivatives and assembled to the biotin linker through a phosphate linkage. The Royal Society of Chemistry.

Flexible stereo- and regioselective synthesis of myo-inositol phosphates (Part 2): Via nonsymmetrical conduritol B derivatives

Podeschwa, Michael A. L.,Plettenburg, Oliver,Altenbach, Hans-Josef

, p. 3116 - 3127 (2007/10/03)

A practical route is described for the preparation of myo-inositol phosphates. Optically pure compounds can be prepared, in both forms, from p-benzoquinone by enzymatic resolution of a diacetoxyconduritol key intermediate. Monosubstituted inositol derivat

Synthesis of mycothiol, 1D-1-O-(2-[N-acetyl-L-cysteinyl]amino-2-deoxy-α-D-glucopyranosyl)-myo-inositol, principal low molecular mass thiol in the actinomycetes

Jardine,Spies, Hendrik S.C,Nkambule, Comfort M,Gammon, David W,Steenkamp, Daniel J

, p. 875 - 881 (2007/10/03)

Members of the actinomycetes produce 1D-1-O-(2-[N-acetyl-l-cysteinyl]amino-2-deoxy-α-D-glucopyranosyl)-myo-inositol or mycothiol 1 as principal low molecular mass thiol. Chemical synthesis of a biosynthetic precursor of mycothiol, the pseudo-disaccharide

The synthesis and resolution of (+/-)-1,4-di-O-benzyl-2,3-O-isopropylidene-myo-inositol

Desai, Trupti,Gigg, Jill,Gigg, Roy,Martin-Zamora, Eloisa,Schnetz, Nathalie

, p. 135 - 144 (2007/10/02)

An improved procedure for the preparation of 1,2-O-isopropylidene-myo-inositol is described.Racemic 1,4-di-O-benzyl-2,3-O-isopropylidene-myo-inositol was prepared by tin-mediated benzylation of 1,2-O-isopropylidene-myo-inositol and resolved readily by cry

The synthesis and resolution of (+/-)-1,5,6-tri-O-benzyl-myo-inositol

Desai, Trupti,Fernandez-Mayoralas, Alfonso,Gigg, Jill,Gigg, Roy,Payne, Sheila

, p. 105 - 123 (2007/10/02)

Racemic 1,5,6-O-benzyl-myo-inositol was prepared by five routes and converted into 1,5,6-tri-O-benzyl-2,3-O-isopropylidene-myo-inositol, the camphanates of which were readily separated by chromatography.The absolute configurations of the chiral derivative

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