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1-O-Benzoyl-2,3:5,6-di-O-isopropylidene-D-talofuranose is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

403604-98-8

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403604-98-8 Usage

Derivation

The compound is derived from D-talofuranose, a type of sugar molecule.

Modification

It has been modified with benzoyl (a phenyl ring with a carbonyl group) and isopropylidene (a dimethylallyl group) groups, which contribute to its unique properties and reactivity.

Potential Applications

The compound has potential applications in the development of new materials and pharmaceuticals, making it valuable for various industries.

Precision

Its precise structure and properties make it a valuable tool for scientists and chemists.

Field of Study

The compound is particularly relevant in the field of carbohydrate chemistry and related disciplines, as it provides insights into the behavior and interactions of complex sugar molecules.

Check Digit Verification of cas no

The CAS Registry Mumber 403604-98-8 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 4,0,3,6,0 and 4 respectively; the second part has 2 digits, 9 and 8 respectively.
Calculate Digit Verification of CAS Registry Number 403604-98:
(8*4)+(7*0)+(6*3)+(5*6)+(4*0)+(3*4)+(2*9)+(1*8)=118
118 % 10 = 8
So 403604-98-8 is a valid CAS Registry Number.

403604-98-8SDS

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 [6-(2,2-dimethyl-1,3-dioxolan-4-yl)-2,2-dimethyl-3a,4,6,6a-tetrahydrofuro[3,4-d][1,3]dioxol-4-yl] benzoate

1.2 Other means of identification

Product number -
Other names 1-O-Benzoyl-2,3:5,6-di-O-isopropylidene-D-talofuranose

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:403604-98-8 SDS

403604-98-8Relevant academic research and scientific papers

One-pot inversion of D-mannono-1,4-lactone for the practical synthesis of L-ribose

Seo, Myung Joon,An, Joungho,Shim, Jae Hak,Kim, Guncheol

, p. 3051 - 3052 (2007/10/03)

L-Ribose was synthesized in a concise manner from D-mannono-1,4-lactone using one-pot inversion conditions. Treatment of D-mannono-1,4-lactone with piperidine, followed by mesylation-induced SN2-type O-alkylation, afforded the desired one-pot inversion in an optimum yield, and the following straightforward transformations provided L-ribose in good yields.

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