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1D-1,2,3,4,5-penta-O-methyl-myo-inositol is a chemical compound derived from myo-inositol, a naturally occurring cyclohexanehexol, which is a sugar alcohol and one of the eight isomers of inositol. In this specific compound, all five hydroxyl groups of myo-inositol are substituted with methyl groups, resulting in a highly modified and stable form of the parent molecule. This modification enhances the compound's solubility and stability, making it useful in various applications, such as pharmaceuticals and chemical research. The compound is characterized by its unique structure and properties, which differentiate it from other inositol isomers and derivatives.

2075-18-5

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2075-18-5 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 2075-18-5 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 2,0,7 and 5 respectively; the second part has 2 digits, 1 and 8 respectively.
Calculate Digit Verification of CAS Registry Number 2075-18:
(6*2)+(5*0)+(4*7)+(3*5)+(2*1)+(1*8)=65
65 % 10 = 5
So 2075-18-5 is a valid CAS Registry Number.

2075-18-5Relevant academic research and scientific papers

Enzyme-catalysed synthesis of galactosylated 1D- and 1L-chiro-inositol, 1D-pinitol, myo-inositol and selected derivatives using the β-galactosidase from the thermophile Thermoanaerobacter sp. strain TP6-B1

Hart, Joanne B.,Kroeger, Lars,Falshaw, Andrew,Falshaw, Ruth,Farkas, Erzsebet,Thiem, Joachim,Win, Anna L.

, p. 1857 - 1871 (2007/10/03)

The products from the enzymatic β-D-galactopyranosylation of 1D-chiro-inositol, 1D-pinitol, 1D-3-O-allyl-4-O-methyl-chiro-inositol, 1D-3,4-di-O-methyl-chiro-inositol, 1L-chiro-inositol and myo-inositol in combined yields ranging from 46% to 64% have been

SYNTHESIS OF SOME BENZYL AND METHYL ETHERS OF myo-INOSITOL

Garegg, Per J.,Lindberg, Bengt,Kvarnstroem, Ingemar,Svensson, Stefan C. T.

, p. 205 - 216 (2007/10/02)

The 1D and 1L forms of 1,2,4,5,6- and 1,2,3,4,5-penta-O-methyl-myo-inositol have been prepared from the corresponding chiral mono-O-benzyl derivatives.Convenient preparations are also described of achiral derivatives of 1-, 2-, 4-, and 5-O-benzyl-myo-inos

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