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165874-26-0

.beta.-D-Allopyranoside, 2-propenyl 2-deoxy-2-(1,3-dihydro-1,3-dioxo-2H-isoindol-2-yl)-4,6-O-(phenylmethylene)is a complex organic compound that features a sugar molecule (allopyranoside) connected to a propenyl group and a phenylmethylene group. Additionally, it includes a 2-deoxy-2-(1,3-dihydro-1,3-dioxo-2H-isoindol-2-yl) moiety. The intricate structure of this compound suggests potential roles in carbohydrate metabolism and possible pharmaceutical applications due to the presence of the isoindol-2-yl group. Further investigation is required to fully understand its biological and chemical characteristics.

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  • 165874-26-0 Structure

  • Basic information

    1. Product Name: .beta.-D-Allopyranoside, 2-propenyl 2-deoxy-2-(1,3-dihydro-1,3-dioxo-2H-isoindol-2-yl)-4,6-O-(phenylmethylene)-
    2. Synonyms: .beta.-D-Allopyranoside, 2-propenyl 2-deoxy-2-(1,3-dihydro-1,3-dioxo-2H-isoindol-2-yl)-4,6-O-(phenylmethylene)-
    3. CAS NO:165874-26-0
    4. Molecular Formula: C24H23NO7
    5. Molecular Weight: 437.44
    6. EINECS: N/A
    7. Product Categories: N/A
    8. Mol File: 165874-26-0.mol

  • Chemical Properties

    1. Melting Point: N/A
    2. Boiling Point: N/A
    3. Flash Point: N/A
    4. Appearance: /
    5. Density: N/A
    6. Refractive Index: N/A
    7. Storage Temp.: N/A
    8. Solubility: N/A
    9. CAS DataBase Reference: .beta.-D-Allopyranoside, 2-propenyl 2-deoxy-2-(1,3-dihydro-1,3-dioxo-2H-isoindol-2-yl)-4,6-O-(phenylmethylene)-(CAS DataBase Reference)
    10. NIST Chemistry Reference: .beta.-D-Allopyranoside, 2-propenyl 2-deoxy-2-(1,3-dihydro-1,3-dioxo-2H-isoindol-2-yl)-4,6-O-(phenylmethylene)-(165874-26-0)
    11. EPA Substance Registry System: .beta.-D-Allopyranoside, 2-propenyl 2-deoxy-2-(1,3-dihydro-1,3-dioxo-2H-isoindol-2-yl)-4,6-O-(phenylmethylene)-(165874-26-0)

  • Safety Data

    1. Hazard Codes: N/A
    2. Statements: N/A
    3. Safety Statements: N/A
    4. WGK Germany:
    5. RTECS:
    6. HazardClass: N/A
    7. PackingGroup: N/A
    8. Hazardous Substances Data: 165874-26-0(Hazardous Substances Data)

165874-26-0 Usage

Uses

Used in Pharmaceutical Industry:
.beta.-D-Allopyranoside, 2-propenyl 2-deoxy-2-(1,3-dihydro-1,3-dioxo-2H-isoindol-2-yl)-4,6-O-(phenylmethylene)is used as a potential pharmaceutical agent for [application reason] due to its unique chemical structure and the presence of the isoindol-2-yl moiety, which may offer specific biological activities.
Used in Carbohydrate Metabolism Research:
In the field of biochemistry, this compound is used as a research tool to study carbohydrate metabolism and its interactions with other biomolecules, given its allopyranoside sugar component and the attached functional groups.

Check Digit Verification of cas no

The CAS Registry Mumber 165874-26-0 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,6,5,8,7 and 4 respectively; the second part has 2 digits, 2 and 6 respectively.
Calculate Digit Verification of CAS Registry Number 165874-26:
(8*1)+(7*6)+(6*5)+(5*8)+(4*7)+(3*4)+(2*2)+(1*6)=170
170 % 10 = 0
So 165874-26-0 is a valid CAS Registry Number.

165874-26-0SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 19, 2017

Revision Date: Aug 19, 2017

1.Identification

1.1 GHS Product identifier

Product name allyl 4,6-O-benzylidene-2-deoxy-2-phthalimido-β-D-allopyranoside

1.2 Other means of identification

Product number -
Other names 2-((4aR,6R,7R,8S,8aS)-6-Allyloxy-8-hydroxy-2-phenyl-hexahydro-pyrano[3,2-d][1,3]dioxin-7-yl)-isoindole-1,3-dione

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:165874-26-0 SDS

165874-26-0Relevant articles and documents

Syntheses of the Fungicide/Insecticide Allosamidin and a Structural Isomer

Blattner, Regine,Furneaux, Richard H.,Kemmitt, timothy,Tyler, Peter C.,Ferrier, Robert J.,Tiden, Anna-Karin

, p. 3411 - 3422 (2007/10/02)

A synthesis of the naturally occurring inhibitor of chitin metabolism, allosamidin 1, involves, as the key step, condensation between the allosamizoline derivative 39, prepared following oxyamination of the cyclopentene 19, and the disaccharide glycosylating agent 54 which was synthesised from 2-acetamido-2-deoxy-D-glucose.The structural isomer 59 of allosamidin is also reported.Brief biological test results obtained using isomers 1 and 59 are recorded.

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