874758-59-5

Basic information

• Product Name: (1R,3S)-3-Acetoxymethyl-8-allyloxy-1-((R)-1-amino-2-hydroxy-ethyl)-7-methoxy-6-methyl-3,4-dihydro-1H-isoquinoline-2-carboxylic acid allyl ester
• Synonyms: (1R,3S)-3-Acetoxymethyl-8-allyloxy-1-((R)-1-amino-2-hydroxy-ethyl)-7-methoxy-6-methyl-3,4-dihydro-1H-isoquinoline-2-carboxylic acid allyl ester
• CAS NO: 874758-59-5
• Molecular Weight: 448.516
• Mol File: 874758-59-5.mol
• Article Data: 0

Chemical Properties

• CAS DataBase Reference: (1R,3S)-3-Acetoxymethyl-8-allyloxy-1-((R)-1-amino-2-hydroxy-ethyl)-7-methoxy-6-methyl-3,4-dihydro-1H-isoquinoline-2-carboxylic acid allyl ester(CAS DataBase Reference)
• NIST Chemistry Reference: (1R,3S)-3-Acetoxymethyl-8-allyloxy-1-((R)-1-amino-2-hydroxy-ethyl)-7-methoxy-6-methyl-3,4-dihydro-1H-isoquinoline-2-carboxylic acid allyl ester(874758-59-5)
• EPA Substance Registry System: (1R,3S)-3-Acetoxymethyl-8-allyloxy-1-((R)-1-amino-2-hydroxy-ethyl)-7-methoxy-6-methyl-3,4-dihydro-1H-isoquinoline-2-carboxylic acid allyl ester(874758-59-5)

Safety Data

• Hazardous Substances Data: 874758-59-5(Hazardous Substances Data)

Usage

Description

(1R,3S)-3-Acetoxymethyl-8-allyloxy-1-((R)-1-amino-2-hydroxy-ethyl)-7-methoxy-6-methyl-3,4-dihydro-1H-isoquinoline-2-carboxylic acid allyl ester is a complex organic molecule with a unique structure that features an isoquinoline core. This molecule is characterized by the presence of multiple functional groups, including an amino group, a hydroxyl group, an ester group, and an allyl group. As a derivative of isoquinoline, it possesses potential pharmaceutical applications due to its diverse structural features and the ability to interact with various biological targets.

Uses

Used in Pharmaceutical Industry:
(1R,3S)-3-Acetoxymethyl-8-allyloxy-1-((R)-1-amino-2-hydroxy-ethyl)-7-methoxy-6-methyl-3,4-dihydro-1H-isoquinoline-2-carboxylic acid allyl ester is used as a pharmaceutical agent for its potential therapeutic effects. The presence of the amino and hydroxyl groups allows for hydrogen bonding and interaction with enzymes and receptors, which can lead to modulation of biological processes. Additionally, the ester and allyl groups may contribute to the molecule's metabolic stability and bioavailability, making it a promising candidate for drug development.
Used in Drug Delivery Systems:
In the field of drug delivery, (1R,3S)-3-Acetoxymethyl-8-allyloxy-1-((R)-1-amino-2-hydroxy-ethyl)-7-methoxy-6-methyl-3,4-dihydro-1H-isoquinoline-2-carboxylic acid allyl ester can be utilized as a component in the design of novel drug delivery systems. Its structural features may enable the development of targeted drug carriers, improving the compound's delivery, bioavailability, and therapeutic efficacy.
Used in Chemical Synthesis:
(1R,3S)-3-Acetoxymethyl-8-allyloxy-1-((R)-1-amino-2-hydroxy-ethyl)-7-methoxy-6-methyl-3,4-dihydro-1H-isoquinoline-2-carboxylic acid allyl ester can also be used as a key intermediate in the synthesis of other complex organic molecules. Its versatile functional groups make it a valuable building block for the creation of new pharmaceuticals, agrochemicals, or other specialty chemicals.

Downstream Products

• 114899-80-8 (1'R,6R,6aR,7R,13S,14R,16R)-5-(acetyloxy)-3',4',6,6a,7,13,14,16-octahydro-6',8-dihydroxy-7',9-dimethoxy-4,10,23-trimethyl-19-oxo-spiro[6,16-(epithiopropanoxymethano)-7,13-imino-12H-1,3-dioxolo[7,8]isoquino[3,2-b][3]benzazocine-20,1'(2'H)-isoquinoline]-14-carbonitrile 
• 114899-77-3 ecteinascidin 743 
• 874758-69-7 C₆₀H₆₁Cl₃N₄O₁₅S