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86042-28-6

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  • High quality 1,5-Di-O-(4-Methylbenzoyl)-2,3-O-Isopropylidene-Β-D- Ribofuranose with high purity

    Cas No: 86042-28-6

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  • 1 Kilogram

  • 30 Metric Ton/Month

  • Simagchem Corporation
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86042-28-6 Usage

Description

1,5-Di-O-(4-methylbenzoyl)-2,3-O-isopropylidene-beta-D-ribofuranose is a complex chemical compound derived from ribofuranose, a type of sugar. It features two 4-methylbenzoyl groups and an isopropylidene group, which contribute to its unique chemical properties. 1,5-Di-O-(4-methylbenzoyl)-2,3-O-isopropylidene-beta-D-ribofuranose has garnered interest in the fields of organic synthesis and medicinal chemistry due to its potential applications in the development of new drugs and as a building block for synthesizing other organic compounds.

Uses

Used in Organic Synthesis:
1,5-Di-O-(4-methylbenzoyl)-2,3-O-isopropylidene-beta-D-ribofuranose is used as a key intermediate in organic synthesis for the creation of various organic compounds. Its unique structure allows for versatile chemical reactions, making it a valuable component in the synthesis of complex organic molecules.
Used in Medicinal Chemistry:
In the field of medicinal chemistry, 1,5-Di-O-(4-methylbenzoyl)-2,3-O-isopropylidene-beta-D-ribofuranose is used as a potential building block for the development of new drugs. Its chemical properties may contribute to the design of novel pharmaceuticals with improved efficacy and selectivity.
Used in Pharmaceutical Industry:
1,5-Di-O-(4-methylbenzoyl)-2,3-O-isopropylidene-beta-D-ribofuranose is used as a precursor in the pharmaceutical industry for the synthesis of drug candidates. Its unique structure and reactivity make it a promising candidate for the development of innovative therapeutic agents.
Used in Research and Development:
1,5-Di-O-(4-methylbenzoyl)-2,3-O-isopropylidene-beta-D-ribofuranose is also used in research and development settings to explore its potential applications and properties further. Scientists and chemists investigate its reactivity, stability, and interactions with other molecules to uncover new ways to utilize it in various chemical and pharmaceutical processes.

Check Digit Verification of cas no

The CAS Registry Mumber 86042-28-6 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 8,6,0,4 and 2 respectively; the second part has 2 digits, 2 and 8 respectively.
Calculate Digit Verification of CAS Registry Number 86042-28:
(7*8)+(6*6)+(5*0)+(4*4)+(3*2)+(2*2)+(1*8)=126
126 % 10 = 6
So 86042-28-6 is a valid CAS Registry Number.
InChI:InChI=1/C24H26O7/c1-14-5-9-16(10-6-14)21(25)27-13-18-19-20(31-24(3,4)30-19)23(28-18)29-22(26)17-11-7-15(2)8-12-17/h5-12,18-20,23H,13H2,1-4H3/t18-,19-,20-,23+/m1/s1

86042-28-6SDS

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 [(3aR,4S,6R,6aR)-2,2-dimethyl-4-(4-methylbenzoyl)oxy-3a,4,6,6a-tetrahydrofuro[3,4-d][1,3]dioxol-6-yl]methyl 4-methylbenzoate

1.2 Other means of identification

Product number -
Other names -

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 -
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More Details:86042-28-6 SDS

86042-28-6Relevant articles and documents

IMPROVED SYNTHESIS OF 2,5-ANHYDRO-D-ALLONITRILE

El Khadem, Hassan S.,Kawai, Joshua

, p. 131 - 138 (2007/10/02)

Two types of mixed ester of β-D-ribofuranose were synthesized.The first had the same groups attached to O-1, 2, and 3, and the second had the same groups attached to O-2,3 and 5.The three esters obtained in the highest yields, starting from D-ribose, were then converted into the halides and nitriles.Of the esters studied, the best suited for conversion into the nitrile was 1-O-acetyl-2,3,5-tri-O-p-toluyl-β-D-ribofuranose, which afforded 2,5-anhydro-3,4,6-tri-O-p-toluyl-D-allonitrile in 60percent yield.

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