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98510-20-4

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98510-20-4 Usage

Uses

1,3,5-O-Methylidyne-myo-inositol is a building block for the synthesis of myo-inositol phosphates.

Check Digit Verification of cas no

The CAS Registry Mumber 98510-20-4 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 9,8,5,1 and 0 respectively; the second part has 2 digits, 2 and 0 respectively.
Calculate Digit Verification of CAS Registry Number 98510-20:
(7*9)+(6*8)+(5*5)+(4*1)+(3*0)+(2*2)+(1*0)=144
144 % 10 = 4
So 98510-20-4 is a valid CAS Registry Number.
InChI:InChI=1/C7H10O6/c8-1-4-2(9)6-3(10)5(1)12-7(11-4)13-6/h1-10H

98510-20-4 Well-known Company Product Price

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  • Aldrich

  • (67550)  1,3,5-O-Methylidyne-myo-inositol  ≥99.0% (HPLC)

  • 98510-20-4

  • 67550-5G

  • 3,245.58CNY

  • Detail

98510-20-4SDS

SAFETY DATA SHEETS

According to Globally Harmonized System of Classification and Labelling of Chemicals (GHS) - Sixth revised edition

Version: 1.0

Creation Date: Aug 12, 2017

Revision Date: Aug 12, 2017

1.Identification

1.1 GHS Product identifier

Product name myo-Inositol monoorthoformate

1.2 Other means of identification

Product number -
Other names myo-inositol 1,3,5-orthoformate

1.3 Recommended use of the chemical and restrictions on use

Identified uses For industry use only.
Uses advised against no data available

1.4 Supplier's details

1.5 Emergency phone number

Emergency phone number -
Service hours Monday to Friday, 9am-5pm (Standard time zone: UTC/GMT +8 hours).

More Details:98510-20-4 SDS

98510-20-4Relevant articles and documents

myo-inositol 4,6-carbonate: An easily prepared small molecule with three syn-axial hydroxyl groups

Angyal

, p. 313 - 320 (2000)

myo-Inositol 4,6-carbonate, a compound having three syn-axial hydroxyl groups, was synthesized in four steps suitable for gram-scale preparation. It readily forms complexes with cations.

First synthesis of 3-O-methyl-scyllo-inosamine, a natural product which favors the Rhizobium-Leguminosae symbiosis

Krief, Alain,Dumont, Willy,Billen, Denis,Letesson, Jean-Jacques,Lestrate, Pascal,Murphy, Peter J.,Lacroix, Damien

, p. 1461 - 1463 (2004)

Rhizopine, extracted in small amounts from nodules induced by Sinorhizobium meliloti strain L5-30 infection of alfalfa, was proved to possess the 3-O-methyl-scyllo-inosamine gross structure.

2-O-Benzoyl-myo-inositol-1,3,5-orthoformate

Samanta, Uttamkumar,Puranik, Vedavati G.,Chakrabarti, Pinak,Thoniyot, Praveen,Shashidhar, Mysore S.

, p. 1289 - 1291 (1998)

Protected myo-inositol derivatives are important precursors in the synthesis of phosphorylated myo-inositol derivatives, which play a significant role in cellular signal transduction. The structure of the title compound, C14H14O

ACETYLATED PRODRUGS FOR DELIVERY ACROSS THE BLOOD-BRAIN BARRIER

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Page/Page column 32 - 34, (2019/11/12)

The present disclosure relates to pharmaceutical compositions including a compound derived from a parent compound having a hydroxyl or amino moiety, wherein the hydroxyl in the parent compound is presented as an ester in the compound or the amino in the parent compound is presented as an amide in the compound, and their use to prevent or treat neurological disease.

4,6-DI-(O-THIOPHOSPHATE)-INOSITOL-1,2,3,5-TETRA-O-SULFATE FOR C. DIFFICILE INFECTION

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Page/Page column 4, (2017/07/23)

The present invention relates to inositol bisthiophosphates-tetrakissulfates, particularly for use in treating symptoms associated with Clostridium difficile infection.

Phosphoric acid phaseomannite class compound and its preparation method and application (by machine translation)

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Paragraph 0355-0357; 0358, (2017/07/14)

The invention discloses a phaseomannite class phosphate compound, phosphoric acid phaseomannite class compound preparation method, and these phosphoric acid phaseomannite class compounds in the preparation of an anti-tumor drug. The use of non-small cell lung cancer cells to the compounds of this invention to inhibit the growth of tumor cells in active testing, that the compounds of this invention have high inhibition of tumor cell growth activity, some of the compound inhibiting activity even with cisplatin active quite, which indicates that the compounds of this invention have good cell penetrability and phosphorus esterase stability, can be used for the development of anti-tumor medicament. (by machine translation)

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