14315-97-0 Usage
Description
1,1,3-Trimethoxypropane, also known as trimethylolpropane, is a clear colorless to light yellow liquid with unique chemical properties. It is an organic compound that belongs to the class of alkyl ethers and is characterized by its three methoxy groups attached to a propane backbone. This versatile molecule has a wide range of applications across different industries due to its chemical reactivity and structural properties.
Uses
Used in Chemical Synthesis Studies:
1,1,3-Trimethoxypropane is used as a synthetic intermediate for the production of various chemicals and compounds. Its ability to react with different reagents makes it a valuable building block in the synthesis of pharmaceuticals, agrochemicals, and other specialty chemicals. The compound's versatility in chemical reactions allows for the creation of a diverse range of products with specific applications.
Used in Pharmaceutical Industry:
1,1,3-Trimethoxypropane is used as a key component in the development of new drugs and drug candidates. Its unique structural properties enable it to interact with biological targets, making it a promising candidate for the treatment of various diseases and medical conditions. Additionally, its compatibility with other molecules allows for the design of drug delivery systems that can improve the bioavailability and efficacy of therapeutic agents.
Used in Agrochemical Industry:
In the agrochemical industry, 1,1,3-Trimethoxypropane is used as a starting material for the synthesis of various pesticides, herbicides, and insecticides. Its chemical reactivity and structural properties make it an ideal candidate for the development of new and improved agrochemicals that can enhance crop protection and yield.
Used in Flavor and Fragrance Industry:
1,1,3-Trimethoxypropane is used as a building block for the creation of various flavor and fragrance compounds. Its ability to react with other molecules allows for the development of unique and complex scents that can be used in the production of perfumes, cosmetics, and other consumer products.
Used in Plastics and Polymer Industry:
1,1,3-Trimethoxypropane is used as a monomer in the production of various types of plastics and polymers. Its chemical properties enable it to be copolymerized with other monomers, resulting in the formation of polymers with specific properties and applications, such as improved strength, flexibility, and durability.
Check Digit Verification of cas no
The CAS Registry Mumber 14315-97-0 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 1,4,3,1 and 5 respectively; the second part has 2 digits, 9 and 7 respectively.
Calculate Digit Verification of CAS Registry Number 14315-97:
(7*1)+(6*4)+(5*3)+(4*1)+(3*5)+(2*9)+(1*7)=90
90 % 10 = 0
So 14315-97-0 is a valid CAS Registry Number.
InChI:InChI=1/C6H14O3/c1-7-5-4-6(8-2)9-3/h6H,4-5H2,1-3H3
14315-97-0Relevant articles and documents
Pd(II)-catalyzed acetalization of terminal olefins with electron-withdrawing groups in supercritical carbon dioxide: selective control and mechanism
Wang, Zhao-Yang,Jiang, Huan-Feng,Ouyang, Xiao-Yue,Qi, Chao-Rong,Yang, Shao-Rong
, p. 9846 - 9854 (2007/10/03)
Pd(II)-catalyzed acetalization of terminal olefins with electron-withdrawing groups was carried out smoothly in supercritical carbon dioxide under oxygen atmosphere when polystyrene-supported benzoquinone (PS-BQ) or CuII (CuI) chloride was employed as cocatalyst. The higher selectivity was achieved, without any chlorinated by-product detected, when using PS-BQ instead of CuII (or CuI) chloride. PS-BQ could be recycled with excellent catalytic activity remaining after each simple filtration. Chlorine ion was demonstrated to be a promoter. The different acetalization mechanisms were revealed by the subtle relationship of chlorine ion and benzoquinone (BQ) to the catalytic activity of PdCl2/PS-BQ, PdII-CuCl2 or Pd(OAc)2/PS-BQ.
Palladium(II)-catalyzed acetalization of allylic acetates and its utilization for the synthesis of 2-cyanovinyl ketones
Hosokawa,Aoki,Murahashi
, p. 558 - 561 (2007/10/02)
α-Cyanoallyl acetate (1 a), when treated with methanol in the presence of bis(acetonitrile)dichloropalladium(II) catalyst, is acetalized at the terminal olefinic carbon to give 1-cyano-3,3-dimethoxypropyl acetate (2). γ-Substituted α-cyanoallyl acetates give 3-substituted 1-cyano-3-oxo-propyl acetates 5 from which 2-cyanovinyl ketones 11 are obtained in good yields.
