119870-20-1 Usage
Description
(R)-2-Benzyloxy-1,3-propanediol 1-(p-toluenesulfonate) is a chemical compound that features a propanediol molecule with a benzyloxy group attached to one of the carbon atoms and a p-toluenesulfonate group. (R)-2-BENZYLOXY-1,3-PROPANEDIOL 1(P-TOLUENESULFONATE) is known for its versatile reactivity and ability to participate in a range of chemical transformations, making it a valuable asset in organic chemistry.
Uses
Used in Pharmaceutical Synthesis:
(R)-2-Benzyloxy-1,3-propanediol 1-(p-toluenesulfonate) is used as a reagent in the synthesis of pharmaceuticals, leveraging its versatile reactivity and ability to undergo various chemical transformations. The p-toluenesulfonate group acts as a leaving group in substitution or elimination reactions, facilitating the creation of new compounds with potential medicinal properties.
Used in Organic Chemistry:
In the field of organic chemistry, (R)-2-Benzyloxy-1,3-propanediol 1-(p-toluenesulfonate) serves as a valuable reagent for conducting a wide array of chemical reactions. Its unique structure allows it to participate in numerous chemical transformations, contributing to the development of novel organic compounds.
Used as a Chiral Building Block:
(R)-2-Benzyloxy-1,3-propanediol 1-(p-toluenesulfonate) is also utilized as a chiral building block in the construction of complex molecules with specific stereochemistry. Its enantiomeric purity is crucial for the synthesis of biologically active compounds, as the stereochemistry of a molecule can significantly influence its biological activity and interactions with target molecules.
Used in Chemical Research:
(R)-2-BENZYLOXY-1,3-PROPANEDIOL 1(P-TOLUENESULFONATE) is employed in chemical research to explore new reaction pathways, develop innovative synthetic methods, and create novel molecules with potential applications in various industries, including pharmaceuticals, materials science, and agrochemicals. Its unique structure and reactivity make it an attractive candidate for studying new chemical phenomena and advancing the field of organic chemistry.
Check Digit Verification of cas no
The CAS Registry Mumber 119870-20-1 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,1,9,8,7 and 0 respectively; the second part has 2 digits, 2 and 0 respectively.
Calculate Digit Verification of CAS Registry Number 119870-20:
(8*1)+(7*1)+(6*9)+(5*8)+(4*7)+(3*0)+(2*2)+(1*0)=141
141 % 10 = 1
So 119870-20-1 is a valid CAS Registry Number.
119870-20-1Relevant articles and documents
Synthesis of optically active lipopeptide analogs from the outer membrane of Escherichia coli
Kurimura,Takemoto,Achiwa
, p. 2590 - 2596 (2007/10/02)
The synthesis of optically active lipopeptide derivatives has been accomplished by the use of chiral glycerol derivatives. Lipopeptide derivatives with (R)-glycerol moieties showed higher mitogenic activities than those with the (S)-configuration. N-2,2,2-Trichloroethoxycarbonyl lipopeptide derivatives increased mitogenic activity.
Synthesis of biologically active acycloazt derivatives and related compounds
Murata,Achiwa
, p. 836 - 838 (2007/10/02)
The synthesis of optically active acyclic analogues of 3'-azido-3'-deoxythymidine, which lack only the 2'-CH2 of the sugar, is described. The synthesis of some nucleoside analogues that contain the N-acetyl-D-neuraminic acid moiety is also described.
