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.beta.-D-Allopyranoside, 2-propenyl 2-deoxy-2-(1,3-dihydro-1,3-dioxo-2H-isoindol-2-yl)-3,6-bis-O-(phenylmethyl)is a complex chemical compound that features a .beta.-D-allopyranoside sugar molecule, a propenyl group, and a 1,3-dihydro-1,3-dioxo-2H-isoindol-2-yl structure. .beta.-D-Allopyranoside, 2-propenyl 2-deoxy-2-(1,3-dihydro-1,3-dioxo-2H-isoindol-2-yl)-3,6-bis-O-(phenylmethyl)-'s unique structure, which includes phenylmethyl groups attached to the allopyranoside, may offer potential applications in various fields such as medicine, pharmaceuticals, and chemical research.

165375-33-7

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165375-33-7 Usage

Uses

Used in Pharmaceutical Industry:
.beta.-D-Allopyranoside, 2-propenyl 2-deoxy-2-(1,3-dihydro-1,3-dioxo-2H-isoindol-2-yl)-3,6-bis-O-(phenylmethyl)is used as a potential pharmaceutical candidate for [application reason] due to its unique structure and potential biological activities.
Used in Chemical Research:
In the field of chemical research, .beta.-D-Allopyranoside, 2-propenyl 2-deoxy-2-(1,3-dihydro-1,3-dioxo-2H-isoindol-2-yl)-3,6-bis-O-(phenylmethyl)is used as a compound for [application reason] because of its complex structure and the possibility of exploring its chemical and biological properties.
Used in Medical Applications:
.beta.-D-Allopyranoside, 2-propenyl 2-deoxy-2-(1,3-dihydro-1,3-dioxo-2H-isoindol-2-yl)-3,6-bis-O-(phenylmethyl)may be used as a potential therapeutic agent for [specific medical condition or application reason] in the medical field, given its unique structural features and potential interactions with biological systems.

Check Digit Verification of cas no

The CAS Registry Mumber 165375-33-7 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,6,5,3,7 and 5 respectively; the second part has 2 digits, 3 and 3 respectively.
Calculate Digit Verification of CAS Registry Number 165375-33:
(8*1)+(7*6)+(6*5)+(5*3)+(4*7)+(3*5)+(2*3)+(1*3)=147
147 % 10 = 7
So 165375-33-7 is a valid CAS Registry Number.

165375-33-7SDS

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 3,6-di-O-benzyl-2-deoxy-2-phthalimido-β-D-allopyranoside

1.2 Other means of identification

Product number -
Other names 2-((2R,3R,4S,5S,6R)-2-Allyloxy-4-benzyloxy-6-benzyloxymethyl-5-hydroxy-tetrahydro-pyran-3-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:165375-33-7 SDS

165375-33-7Relevant academic research and scientific papers

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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