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1,4-Dioxaspiro[4.5]decane-2-methanol, (R)is a unique spiroketal chemical compound characterized by its complex and specific structure, featuring a spirotetrahydrofuran ring system. The (R)designation signifies its distinct stereochemistry, which is crucial for its potential applications in various chemical and pharmaceutical processes. 1,4-Dioxaspiro[4.5]decane-2-methanol, (R)may serve as a valuable building block for synthesizing other complex organic molecules or as a starting material for the production of pharmaceutical drugs, owing to its unique structural properties.

113798-80-4

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113798-80-4 Usage

Uses

Used in Chemical Synthesis:
1,4-Dioxaspiro[4.5]decane-2-methanol, (R)is used as a building block in chemical synthesis for the creation of other complex organic molecules. Its unique spiroketal structure and stereochemistry make it a valuable component in the development of novel compounds with specific properties and applications.
Used in Pharmaceutical Industry:
1,4-Dioxaspiro[4.5]decane-2-methanol, (R)is used as a starting material in the pharmaceutical industry for the production of drugs. Its specific structure and stereochemistry may contribute to the development of new pharmaceutical compounds with targeted therapeutic effects, potentially leading to the discovery of innovative treatments for various medical conditions.
Used in Research and Development:
1,4-Dioxaspiro[4.5]decane-2-methanol, (R)is utilized in research and development for studying its unique properties and exploring its potential applications in various fields. 1,4-Dioxaspiro[4.5]decane-2-methanol, (R)-'s specific stereochemistry and spiroketal structure make it an interesting subject for scientific investigation, which may lead to new insights and advancements in chemistry and related disciplines.

Check Digit Verification of cas no

The CAS Registry Mumber 113798-80-4 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,1,3,7,9 and 8 respectively; the second part has 2 digits, 8 and 0 respectively.
Calculate Digit Verification of CAS Registry Number 113798-80:
(8*1)+(7*1)+(6*3)+(5*7)+(4*9)+(3*8)+(2*8)+(1*0)=144
144 % 10 = 4
So 113798-80-4 is a valid CAS Registry Number.

113798-80-4SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 19, 2017

Revision Date: Aug 19, 2017

1.Identification

1.1 GHS Product identifier

Product name [(3R)-1,4-dioxaspiro[4.5]decan-3-yl]methanol

1.2 Other means of identification

Product number -
Other names [2R]-1,4-dioxa-spiro[4,5]dec-2-yl-methanol

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:113798-80-4 SDS

113798-80-4Relevant academic research and scientific papers

Application of pig liver esterase catalyzed transesterification in organic media to the kinetic resolution of glycerol derivatives

Jungen, Manfred,Gais, Hans-Joachim

, p. 3747 - 3758 (1999)

The PLE/MPEG catalyzed transesterification of the glycerol ketals rac-1a and rac-1d-f with vinyl propionate in toluene proceeded with good selectivities (E=24-34) and gave the enantiomerically enriched S-alcohols 1a and 1d-f, and the S-esters 2a and 2d-f. High selectivities (E=99 and E≥200) were observed in the transesterification of the glycerol ether rac-3 and its desoxy analog rac-5, both having a secondary hydroxy group, with PLE/MPEG. In transesterifications in organic media PLE exhibited a much higher enantioselectivity than in hydrolysis in water.

Organocatalytic kinetic resolution of racemic primary alcohols using a chiral 1,2-diamine derived from (S)-proline

Terakado, Dai,Koutaka, Hitomi,Oriyama, Takeshi

, p. 1157 - 1165 (2007/10/03)

A highly efficient and good enantioselective organocatalytic asymmetric acylation of racemic primary alcohols with acyl chlorides has been achieved catalyzed by a chiral 1,2-diamine derived from (S)-proline.

EFFICIENT RESOLUTION OF SECONDARY ALCOHOLS, CYANOHYDRINS, AND GLYCEROL ACETALS BY COMPLEXATION WITH THE HOST DERIVED FROM TARTARIC ACID

Toda, Fumio,Matsuda, Shotaro,Tanaka, Koichi

, p. 983 - 986 (2007/10/02)

Some title hydroxy compounds were resolved efficiently by complexation with the host compounds derived from tartaric acid.

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