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1,4:3,6-dianhydro-2,5-di-O-benzylhexitol is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

6338-36-9

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6338-36-9 Usage

Appearance

White crystalline

Natural occurrence

Not naturally occurring

Parent compound

Isosorbide (a six-membered sugar alcohol)

Derivative

Di-benzylated derivative

Usage

Intermediate in the synthesis of various pharmaceuticals

Applications

Cardiovascular and diuretic pharmaceuticals

Additional uses

Starting material in the manufacture of specialty polymers and resins

Structure

Unique structure useful in the development of new materials and pharmaceuticals with specific properties and applications.

Check Digit Verification of cas no

The CAS Registry Mumber 6338-36-9 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 6,3,3 and 8 respectively; the second part has 2 digits, 3 and 6 respectively.
Calculate Digit Verification of CAS Registry Number 6338-36:
(6*6)+(5*3)+(4*3)+(3*8)+(2*3)+(1*6)=99
99 % 10 = 9
So 6338-36-9 is a valid CAS Registry Number.

6338-36-9SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 15, 2017

Revision Date: Aug 15, 2017

1.Identification

1.1 GHS Product identifier

Product name (3S,3aR,6R,6aR)-3,6-bis(phenylmethoxy)-2,3,3a,5,6,6a-hexahydrofuro[3,2-b]furan

1.2 Other means of identification

Product number -
Other names di-O-benzoyl-Lg-tartaric acid dipropyl ester

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:6338-36-9 SDS

6338-36-9Relevant academic research and scientific papers

Synthesis of novel chiral imidazolium-based ionic liquids derived from isosorbide and their applications in asymmetric aza Diels-Alder reaction

Nguyen Van Buu, Olivier,Aupoix, Audrey,Vo-Thanh, Giang

experimental part, p. 2260 - 2265 (2009/07/18)

A novel family of chiral imidazolium-based ionic liquids containing a chiral moiety and a free hydroxyl function has been designed and synthesized using isosorbide as a biorenewable substrate. These chiral ionic liquids were found to catalyze the aza Diels-Alder reaction to give good yields and moderate diastereoselectivities. Chiral ionic liquids are recycled while their efficiency is preserved.

Chiral ionic liquids derived from isosorbide: Synthesis, properties and applications in asymmetric synthesis

Van Buu, Olivier Nguyen,Aupoix, Audrey,Hong, Nhung Doan Thi,Vo-Thanh, Giang

scheme or table, p. 2060 - 2072 (2009/12/25)

A novel class of chiral ammonium and imidazolium-based ionic liquids has been designed and synthesized using isosorbide as a biorenewable substrate. These chiral ionic liquids were found to catalyze the aza Diels-Alder reaction to give good yields and moderate diastereoselectivitives.

Ethers of bisanhydrohexitols

-

Page/Page column 2, (2008/06/13)

A novel method for the synthesis of ethers of anhydrosugars, such as isosorbide, isomannide, and isoidide, is disclosed. The bisglycidyl ethers are useful as substitutes for bisphenol A in the manufacture of thermoset epoxy ethers. Anhydrosugar ethers are

Selective alkylations of 1,4:3,6-dianhydro-D-glucitol (isosorbide)

Abenhaiem, D.,Loupy, A.,Munnier, L.,Tamion, R.,Marsais, F.,Queguiner, G.

, p. 255 - 266 (2007/10/02)

Each of the two hydroxyl groups of isosorbide can be alkylated selectively, either by direct alkylation with benzyl chloride or allyl bromide according to the reaction conditions, or by a three-step procedure involving selective monoacetylation, alkylation with four different reagents, and finally deacetylation.Monobutyl and monomethyl derivatives from isosorbide are also described.

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