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19895-66-0

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19895-66-0 Usage

General Description

Dianhydromannitol is a chemical compound with the molecular formula C6H8O4. It is a sugar alcohol derivative, specifically a derivative of mannitol. dianhydromannitol is also known as mannitol anhydride or osmitrolanhydride. Dianhydromannitol is used in the production of high-performance polymers, such as epoxy resins, and as a substrate for the synthesis of various pharmaceuticals. It is also used as a crosslinking agent in the preparation of polyanhydride copolymers. Furthermore, dianhydromannitol has potential applications in the development of biodegradable and controlled-release drug delivery systems. Overall, dianhydromannitol exhibits a wide range of potential uses in various industrial and pharmaceutical applications.

Check Digit Verification of cas no

The CAS Registry Mumber 19895-66-0 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 1,9,8,9 and 5 respectively; the second part has 2 digits, 6 and 6 respectively.
Calculate Digit Verification of CAS Registry Number 19895-66:
(7*1)+(6*9)+(5*8)+(4*9)+(3*5)+(2*6)+(1*6)=170
170 % 10 = 0
So 19895-66-0 is a valid CAS Registry Number.
InChI:InChI=1/C6H10O4/c7-5(3-1-9-3)6(8)4-2-10-4/h3-8H,1-2H2

19895-66-0SDS

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 hexa-1,5-diene-2,3,4,5-tetrol

1.2 Other means of identification

Product number -
Other names dianhydromannitol

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:19895-66-0 SDS

19895-66-0Relevant articles and documents

CuAAC click chemistry with N-propargyl 1,5-dideoxy-1,5-imino-D-gulitol and N-propargyl 1,6-dideoxy-1,6-imino-D-mannitol provides access to triazole-linked piperidine and azepane pseudo-disaccharide iminosugars displaying glycosidase inhibitory properties

Zamoner, Luís Otávio B.,Arag?o-Leoneti, Valquíria,Mantoani, Susimaire P.,Rugen, Michael D.,Nepogodiev, Sergey A.,Field, Robert A.,Carvalho, Ivone

, p. 29 - 37 (2016)

Protecting group-free synthesis of 1,2:5,6-di-anhydro-D-mannitol, followed by ring opening with propargylamine and subsequent ring closure produced a separable mix of piperidine N-propargyl 1,5-dideoxy-1,5-imino-D-gulitol and azepane N-propargyl 1,6-dideo

Solid phase synthesis of (R)- and (S)-[13C]-butadiene monoxide

Claffey, David J.,Ruth, James A.

, p. 3715 - 3716 (2007/10/03)

A stereospecific route to (R)- and (S)-[13C]-butadiene monoxide was developed using (R)- or (S)- glycidaldehyde and a polymer-supported Wittig reagent.

Inversion of Enantioselectivity in the Kinetic Resolution Mode of the Katsuki-Sharpless Asymmetric Epoxidation Reaction

Takano, Seiichi,Iwabuchi, Yoshiharu,Ogasawara, Kunio

, p. 2786 - 2787 (2007/10/02)

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