Cost-effective and customizable 3β-[(2`-hydroxybenzoyl)oxy]-1R-(exo,exo)-8-methyl-8-azabicyclo[3.2.1]octane-2-carboxylic acid methyl ester 89339-17-3 supplier

Q: What is the 3ß-[(2`-hydroxybenzoyl)oxy]-1R-(exo,exo)-8-methyl-8-azabicyclo[3.2.1]octane-2-carboxylic acid methyl ester?

3ß-[(2`-hydroxybenzoyl)oxy]-1R-(exo,exo)-8-methyl-8-azabicyclo[3.2.1]octane-2-carboxylic acid methyl ester is , while it's Molecular Formula is C 17 H 21 NO 5 . Used in Pharmaceutical Industry: 3ß-[(2`-hydroxybenzoyl)oxy]-1R-(exo,exo)-8-methyl-8-azabicyclo[3.2.1]octane-2-carboxylic acid methyl ester is utilized as an intermediate in the synthesis of various pharmaceutical compounds for medicinal purposes. Its unique structure and functional groups contribute to the development of new drugs with potential therapeutic applications. Used in Drug Synthesis: In the field of drug synthesis, 3ß-[(2`-hydroxybenzoyl)oxy]-1R-(exo,exo)-8-methyl-8-azabicyclo[3.2.1]octane-2-carboxylic acid methyl ester serves as a key component in the creation of novel pharmaceutical agents. Its presence in the molecular structure can influence the pharmacokinetics, pharmacodynamics, and overall efficacy of the resulting drug molecules. Used in Medicinal Research: 3ß-[(2`-hydroxybenzoyl)oxy]-1R-(exo,exo)-8-methyl-8-azabicyclo[3.2.1]octane-2-carboxylic acid methyl ester is employed as a research tool in medicinal chemistry to explore its potential interactions with biological targets. Understanding these interactions can lead to the discovery of new therapeutic agents and a deeper comprehension of molecular mechanisms in disease processes. Used in Drug Development: In the drug development process, 3ß-[(2`-hydroxybenzoyl)oxy]-1R-(exo,exo)-8-methyl-8-azabicyclo[3.2.1]octane-2-carboxylic acid methyl ester is leveraged to create prototypes and test compounds for preclinical and clinical studies. Its unique properties can aid in optimizing drug candidates for safety, efficacy, and pharmacological profile.

Q: What is the CAS number for 3ß-[(2`-hydroxybenzoyl)oxy]-1R-(exo,exo)-8-methyl-8-azabicyclo[3.2.1]octane-2-carboxylic acid methyl ester?

The CAS number of 3ß-[(2`-hydroxybenzoyl)oxy]-1R-(exo,exo)-8-methyl-8-azabicyclo[3.2.1]octane-2-carboxylic acid methyl ester is 89339-17-3.

Q: What is 3ß-[(2`-hydroxybenzoyl)oxy]-1R-(exo,exo)-8-methyl-8-azabicyclo[3.2.1]octane-2-carboxylic acid methyl ester (89339-17-3) used for?

3ß-[(2`-hydroxybenzoyl)oxy]-1R-(exo,exo)-8-methyl-8-azabicyclo[3.2.1]octane-2-carboxylic acid methyl ester is a complex organic chemical compound characterized by a bicyclic structure with a carboxylic acid and a methyl ester group. 3ß-[(2`-hydroxybenzoyl)oxy]-1R-(exo,exo)-8-methyl-8-azabicyclo[3.2.1]octane-2-carboxylic acid methyl ester features a benzoyl group and a hydroxyl group attached to the bicyclic framework, making it a versatile molecule in pharmaceutical applications. As a derivative of a bicyclic compound, it is highly valued in drug synthesis and research due to its unique structural and functional attributes.

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3β-[(2`-hydroxybenzoyl)oxy]-1R-(exo,exo)-8-methyl-8-azabicyclo[3.2.1]octane-2-carboxylic acid methyl ester

CAS No.: 89339-17-3
Purity: 99%

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Cost-effective and customizable 3β-[(2`-hydroxybenzoyl)oxy]-1R-(exo,exo)-8-methyl-8-azabicyclo[3.2.1]octane-2-carboxylic acid methyl ester 89339-17-3 supplier

Molecular Formula: C₁₇H₂₁NO₅
Molecular Weight: 319.357
Boiling Point: 416.2±45.0 °C(Predicted)
Density: 1.30±0.1 g/cm3(Predicted)

89339-17-3 Relevant articles

Synthesis and dopamine transporter binding of 2'-substituted cocaine analogs

El-Moselhy, Tarek F.,Avor, Kwasi S.,Basmadjian, Garo P.

, p. 50 - 57 (2007/10/03)

A series of 2'-substituted cocaine analo...

89339-17-3 Process route

: 192648-66-1
3-[(2'-acetoxybenzoyl)oxy]-[1R-(exo,exo)]-8-methyl-8-azabicyclo[3.2.1]octane-2-carboxylic acid methyl ester

: 89339-17-3
3β-[(2`-hydroxybenzoyl)oxy]-1R-(exo,exo)-8-methyl-8-azabicyclo[3.2.1]octane-2-carboxylic acid methyl ester

Conditions

Conditions	Yield
With hydrogenchloride; In methanol; for 48h; Heating;	94%

: 5796-31-6
ecgonine hydrochloride

: 89339-17-3
3β-[(2`-hydroxybenzoyl)oxy]-1R-(exo,exo)-8-methyl-8-azabicyclo[3.2.1]octane-2-carboxylic acid methyl ester

Conditions

Conditions	Yield
Multi-step reaction with 3 steps 1: HCl gas 2: Et₃N / benzene / 40 °C 3: 94 percent / HCl gas / methanol / 48 h / Heating With hydrogenchloride; triethylamine; In methanol; benzene;

89339-17-3 Upstream products

192648-66-1
3-[(2'-acetoxybenzoyl)oxy]-[1R-(exo,exo)]-8-methyl-8-azabicyclo[3.2.1]octane-2-carboxylic acid methyl ester
5796-31-6
ecgonine hydrochloride
7143-09-1
methyl ecgonine
50-36-2
Cocaine