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3-O-benzyl-1,2-isopropylidene-5,6-di-O-(3-methyl-2-butenyl)-α-D-glucofuranose is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

410087-87-5

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410087-87-5 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 410087-87-5 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 4,1,0,0,8 and 7 respectively; the second part has 2 digits, 8 and 7 respectively.
Calculate Digit Verification of CAS Registry Number 410087-87:
(8*4)+(7*1)+(6*0)+(5*0)+(4*8)+(3*7)+(2*8)+(1*7)=115
115 % 10 = 5
So 410087-87-5 is a valid CAS Registry Number.

410087-87-5SDS

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 3-O-benzyl-1,2-isopropylidene-5,6-di-O-(3-methyl-2-butenyl)-α-D-glucofuranose

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

More Details:410087-87-5 SDS

410087-87-5Relevant academic research and scientific papers

The prenyl group: A versatile hydroxy protecting group, removable chemoselectively under mild conditions

Vatèle, Jean-Michel

, p. 5689 - 5698 (2002)

Iodine in dichloromethane (in the presence of 3? molecular sieves for acid-sensitive substrates) and 2,3-dichloro-5,6-dicyanoquinone (DDQ) in dichloromethane-water (9:1) are mild and efficient methods to cleave prenyl ethers. These reaction conditions are compatible with the presence of other protecting groups such as acetals, acetates, allyl, benzyl and TBDPS groups. Exposure of aryl prenyl ethers to iodine led to the formation of 3-iodo-2,2-dimethylchroman derivatives in acceptable yields via a tandem Friedel-Crafts/iodocyclization reactions. Facile one-step transformation of two iodinated dimethylchroman derivatives allowed the synthesis of natural flavanoids among them: zanthoxylol, an anti-sickling agent.

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