19895-66-0 Usage
Description
Dianhydromannitol, also known as mannitol anhydride or osmitrolanhydride, is a sugar alcohol derivative with the molecular formula C6H8O4. It is derived from mannitol and is a chemical compound with potential applications in various industrial and pharmaceutical fields.
Uses
Used in High-Performance Polymers:
Dianhydromannitol is used as a key component in the production of high-performance polymers, such as epoxy resins. Its unique properties contribute to the enhanced performance and durability of these materials.
Used in Pharmaceutical Synthesis:
Dianhydromannitol serves as a substrate for the synthesis of various pharmaceuticals. Its chemical structure allows for the development of new drugs with potential therapeutic benefits.
Used as a Crosslinking Agent:
In the preparation of polyanhydride copolymers, dianhydromannitol is used as a crosslinking agent. This application enhances the stability and performance of the resulting polymers.
Used in Biodegradable and Controlled-Release Drug Delivery Systems:
Dianhydromannitol has potential applications in the development of biodegradable and controlled-release drug delivery systems. Its properties make it a promising candidate for improving the efficiency and safety of drug administration.
Overall, dianhydromannitol exhibits a wide range of potential uses in various industries, including polymer production, pharmaceutical synthesis, and drug delivery systems, making it a valuable compound for further research and development.
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
19895-66-0Relevant 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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