39562-58-8 Usage
Description
4,4-Dimethoxybutan-2-ol, also known as 3-Hydroxybutyraldehyde Dimethyl Acetal, is an organic compound with the molecular formula C6H14O3. It is a colorless liquid with a mild, pleasant odor. 4,4-Dimethoxybutan-2-ol is characterized by its two methoxy groups (-OCH3) attached to the fourth carbon and a hydroxyl group (-OH) attached to the second carbon. Its structure endows it with unique chemical properties, making it a versatile intermediate in various synthetic applications.
Uses
Used in Chemical Synthesis:
4,4-Dimethoxybutan-2-ol is used as an intermediate in the chemical synthesis of aldols and aldol polymerization. Its ability to form aldols, which are important in the construction of complex organic molecules, makes it a valuable compound in the field of organic chemistry. The aldol reaction is a fundamental carbon-carbon bond-forming process that allows for the creation of a wide range of chemical structures.
Used in Paper Industry:
In the paper industry, 4,4-Dimethoxybutan-2-ol is used in the synthesis of model polymers for paper wet strengthening. 4,4-Dimethoxybutan-2-ol contributes to the development of polymers that can enhance the strength and durability of paper when it is exposed to moisture. This application is particularly important for improving the performance of paper products in various environments and conditions.
Used in Pharmaceutical Industry:
Although not explicitly mentioned in the provided materials, 4,4-Dimethoxybutan-2-ol, due to its structural features, could potentially be used in the pharmaceutical industry as a building block for the synthesis of complex drug molecules. Its ability to form diverse chemical structures makes it a promising candidate for the development of new drugs with specific therapeutic properties.
Check Digit Verification of cas no
The CAS Registry Mumber 39562-58-8 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 3,9,5,6 and 2 respectively; the second part has 2 digits, 5 and 8 respectively.
Calculate Digit Verification of CAS Registry Number 39562-58:
(7*3)+(6*9)+(5*5)+(4*6)+(3*2)+(2*5)+(1*8)=148
148 % 10 = 8
So 39562-58-8 is a valid CAS Registry Number.
InChI:InChI=1/C6H14O3/c1-5(7)4-6(8-2)9-3/h5-7H,4H2,1-3H3
39562-58-8Relevant articles and documents
PANTETHEINE DERIVATIVES AND USES THEREOF
-
Paragraph 2121, (2020/06/19)
The present disclosure relates to compounds of Formula (I), (II), or (II'): (I), (II), (II'), and pharmaceutically acceptable salts or solvates thereof. The present disclosure also relates to pharmaceutical compositions comprising the compounds and therapeutic and diagnostic uses of the compounds and pharmaceutical compositions.
α-Amino Acid-Isosteric α-Amino Tetrazoles
Zhao, Ting,Kurpiewska, Katarzyna,Kalinowska-T?us?cik, Justyna,Herdtweck, Eberhardt,D?mling, Alexander
supporting information, p. 3009 - 3018 (2016/03/26)
The synthesis of all 20 common natural proteinogenic and 4 otherα-amino acid-isosteric α-amino tetrazoles has been accomplished, whereby the carboxyl group is replaced by the isosteric 5-tetrazolyl group. The short process involves the use of the key Ugi tetrazole reaction followed by deprotection chemistries. The tetrazole group is bioisosteric to the carboxylic acid and is widely used in medicinal chemistry and drug design. Surprisingly, several of the common α-amino acid-isosteric α-amino tetrazoles are unknown up to now. Therefore a rapid synthetic access to this compound class and non-natural derivatives is of high interest to advance the field.
Aldolase catalyzed stereoselective synthesis of arabinohexulose, xyloheptulose, threohexulose and xylohexulose
-
, (2008/06/13)
The present invention relates to aldolase catalyzed stereo-selective synthesis of sugars and compositions of matter comprising arabinohexulose, xyloheptulose, threohexulose, and xylohexulose.
