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2,3:5,6-DI-O-ISOPROPYLIDENE-L-MANNOFURANOSE is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

84857-03-4

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84857-03-4 Usage

Molecular weight

304.35 g/mol

Structure

A derivative of mannose with two isopropylidene groups attached at the 2,3 and 5,6 positions.

Functional groups

Hydroxyl groups, isopropylidene groups.

Use as protecting group

It is commonly used as a protecting group for the hydroxyl groups in carbohydrates during organic synthesis.

Synthesis of complex carbohydrates

It is used as a building block in the synthesis of complex carbohydrates.

Potential applications

It has potential applications in pharmaceuticals, materials science, and chemical biology for the creation of novel molecules.

Check Digit Verification of cas no

The CAS Registry Mumber 84857-03-4 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 8,4,8,5 and 7 respectively; the second part has 2 digits, 0 and 3 respectively.
Calculate Digit Verification of CAS Registry Number 84857-03:
(7*8)+(6*4)+(5*8)+(4*5)+(3*7)+(2*0)+(1*3)=164
164 % 10 = 4
So 84857-03-4 is a valid CAS Registry Number.

84857-03-4SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 17, 2017

Revision Date: Aug 17, 2017

1.Identification

1.1 GHS Product identifier

Product name 2,3:5,6-DI-O-ISOPROPYLIDENE-L-MANNOFURANOSE

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:84857-03-4 SDS

84857-03-4Downstream Products

84857-03-4Relevant articles and documents

Synthetic studies on halichondrins: A new practical synthesis of the C.1-C.12 segment

Duan,Kishi

, p. 7541 - 7544 (1993)

A new practical synthesis of the C.1-C.12 halichondrin segment was achieved from L-mannonic γ-lactone (5), using osmylation, C-allylation and Michael reaction as key steps.

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