57371-44-5 Usage
Description
3-(4-(Benzyloxy)-3-Methoxyphenyl)propan-1-ol, also known as 3-(4-(Benzyloxy)-3-Methoxyphenyl)propanol, is a versatile chemical compound with the molecular formula C17H20O3. It is a colorless liquid that features a benzyl ether group, a methoxy group, and a hydroxyl group. These functional groups make it a valuable building block in organic synthesis and pharmaceutical research, often utilized as an intermediate in the production of pharmaceuticals and agrochemicals. Its unique structure also offers potential for the development of new drugs and materials, and it is widely used in academic and industrial research laboratories.
Uses
Used in Pharmaceutical Research and Development:
3-(4-(Benzyloxy)-3-Methoxyphenyl)propan-1-ol is used as a key intermediate in the synthesis of various pharmaceuticals for its ability to be incorporated into complex molecular structures, contributing to the development of new drugs with potential therapeutic applications.
Used in Agrochemical Production:
In the agrochemical industry, 3-(4-(Benzyloxy)-3-Methoxyphenyl)propan-1-ol serves as an intermediate in the creation of compounds that can be used in pest control and crop protection, leveraging its chemical properties to enhance the effectiveness of these products.
Used in Organic Synthesis:
3-(4-(Benzyloxy)-3-Methoxyphenyl)propan-1-ol is utilized as a versatile building block in organic synthesis, allowing chemists to construct a wide range of organic compounds for various applications, from materials science to specialty chemicals.
Used in Academic Research:
3-(4-(Benzyloxy)-3-Methoxyphenyl)propan-1-ol is a popular subject of study in academic research settings, where its unique structure and functional groups are investigated for potential applications in new areas of chemistry and related fields, fostering innovation and scientific discovery.
Used in Industrial Research Laboratories:
In industrial research, 3-(4-(Benzyloxy)-3-Methoxyphenyl)propan-1-ol is employed for its potential to contribute to the development of new materials and chemical processes, driving advancements in various industries that rely on novel chemical compounds.
Check Digit Verification of cas no
The CAS Registry Mumber 57371-44-5 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 5,7,3,7 and 1 respectively; the second part has 2 digits, 4 and 4 respectively.
Calculate Digit Verification of CAS Registry Number 57371-44:
(7*5)+(6*7)+(5*3)+(4*7)+(3*1)+(2*4)+(1*4)=135
135 % 10 = 5
So 57371-44-5 is a valid CAS Registry Number.
57371-44-5Relevant articles and documents
First Enantioselective Synthesis of Surinamensinol B and a Non-Natural Polysphorin Analogue by a Two-Stereocentered Hydrolytic Kinetic Resolution
Lalwani, Komal G.,Sudalai, Arumugam
, p. 7344 - 7351 (2015/11/25)
An efficient and economical approach to the synthesis of antitumor and anti-inflammatory surinamensinol B (1) and antimalarial polysphorin analogue 2 has been achieved with high enantiomeric purity (96 % ee) by starting from commercially available 3,4,5-trimethoxybenzaldehyde. The key steps of the strategy include a Co-catalyzed two-stereocentered hydrolytic kinetic resolution (HKR) of racemic 2-[(methoxymethoxy)(3,4,5-trimethoxyphenyl)methyl]oxirane (13) as the chiral inducing step followed by a Mitsunobu reaction. Chiral epoxide 14 and chiral diol 15 were utilized in the syntheses of both compounds.
The first stereoselective total synthesis of a new antitumour and anti-inflammatory neolignan, surinamensinol A
Reddy, Parigi Raghavendar,Das, Biswanath
, p. 7432 - 7434 (2014/02/14)
The stereoselective total synthesis of an antitumour and anti-inflammatory 8-O-4′-neolignan, surinamensinol A has been accomplished starting from two aldehydes, 3,4,5-trimethoxy benzaldehyde and vanillin. The key steps involve an asymmetric reduction using a chiral oxazaborolidine complex, a Sharpless asymmetric dihydroxyllation and a Mitsunobu reaction. This is the first report of the total synthesis of surinamensinol A.
Synthesis of gingerol and diarylheptanoids
Sabitha, Gowravaram,Srinivas, Chitti,Reddy, Teega Rammohan,Yadagiri, Kurra,Yadav, Jhillu Singh
experimental part, p. 2124 - 2133 (2012/03/27)
The synthesis of gingerol 1 and related compounds 2-5 along with diarylheptanoids 6-8 has been accomplished using a Keck allylation, Crimmins' aldol reaction, aldehyde coupling with acetylene, and chelation controlled reductions as the key reactions. The absolute configuration of these molecules was confirmed by preparing their acetonide derivatives and by comparison of the NMR data with natural compounds.
