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α,α-Bis(hydroxymethyl)benzeneacetic acid (1R,5S)-8-methyl-8-azabicyclo[3.2.1]oct-3α-yl ester is a complex organic compound derived from the synthesis of atropine, a well-known muscarinic antagonist. It is characterized by its unique molecular structure, which includes a benzeneacetic acid backbone with hydroxymethyl groups and an eight-membered azabicyclo ring. α,α-Bis(hydroxymethyl)benzeneacetic acid (1R,5S)-8-methyl-8-azabicyclo[3.2.1]oct-3α-yl ester has the potential for various applications due to its structural properties and functional groups.

2515-36-8

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2515-36-8 Usage

Uses

Used in Pharmaceutical Industry:
α,α-Bis(hydroxymethyl)benzeneacetic acid (1R,5S)-8-methyl-8-azabicyclo[3.2.1]oct-3α-yl ester is used as an intermediate in the synthesis of various pharmaceutical compounds, particularly those with muscarinic antagonist properties. Its unique structure allows for the development of new drugs with potential applications in treating conditions such as asthma, chronic obstructive pulmonary disease (COPD), and other respiratory disorders.
Used in Chemical Research:
α,α-Bis(hydroxymethyl)benzeneacetic acid (1R,5S)-8-methyl-8-azabicyclo[3.2.1]oct-3α-yl ester serves as a valuable research tool for chemists and biologists studying the structure-activity relationships of atropine and its derivatives. It can be used to investigate the effects of structural modifications on the biological activity and pharmacological properties of these compounds.
Used in Drug Development:
α,α-Bis(hydroxymethyl)benzeneacetic acid (1R,5S)-8-methyl-8-azabicyclo[3.2.1]oct-3α-yl ester can be utilized in the development of novel drug candidates with improved efficacy, selectivity, and safety profiles. Its unique structural features may provide new avenues for the design of more potent and selective muscarinic antagonists.
Used in Quality Control and Standardization:
As a byproduct of atropine synthesis, α,α-Bis(hydroxymethyl)benzeneacetic acid (1R,5S)-8-methyl-8-azabicyclo[3.2.1]oct-3α-yl ester can be used for quality control and standardization purposes in the pharmaceutical industry. It can help ensure the purity and consistency of atropine and its derivatives, which is crucial for their safety and efficacy in medical applications.

Check Digit Verification of cas no

The CAS Registry Mumber 2515-36-8 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 2,5,1 and 5 respectively; the second part has 2 digits, 3 and 6 respectively.
Calculate Digit Verification of CAS Registry Number 2515-36:
(6*2)+(5*5)+(4*1)+(3*5)+(2*3)+(1*6)=68
68 % 10 = 8
So 2515-36-8 is a valid CAS Registry Number.
InChI:InChI=1/C18H25NO4/c1-19-14-7-8-15(19)10-16(9-14)23-17(22)18(11-20,12-21)13-5-3-2-4-6-13/h2-6,14-16,20-21H,7-12H2,1H3/t14-,15+,16?

2515-36-8SDS

SAFETY DATA SHEETS

According to Globally Harmonized System of Classification and Labelling of Chemicals (GHS) - Sixth revised edition

Version: 1.0

Creation Date: Aug 13, 2017

Revision Date: Aug 13, 2017

1.Identification

1.1 GHS Product identifier

Product name α-Hydroxymethyl Atropine

1.2 Other means of identification

Product number -
Other names (8-methyl-8-azabicyclo[3.2.1]octan-3-yl) 3-hydroxy-2-(hydroxymethyl)-2-phenylpropanoate

1.3 Recommended use of the chemical and restrictions on use

Identified uses For industry use only.
Uses advised against no data available

1.4 Supplier's details

1.5 Emergency phone number

Emergency phone number -
Service hours Monday to Friday, 9am-5pm (Standard time zone: UTC/GMT +8 hours).

More Details:2515-36-8 SDS

2515-36-8Upstream product

2515-36-8Downstream Products

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