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273376-39-9

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273376-39-9 Usage

General Description

8-Azabicyclo[3.2.1]octane-8-carboxylic acid, 3-(hydroxymethyl)-, 1,1-dimethylethyl ester, (3-endo)- is a chemical compound with the molecular formula C13H23NO3. It is a derivative of 8-azabicyclo[3.2.1]octane, and it is commonly used as a building block in the synthesis of various pharmaceuticals and agrochemicals. 8-Azabicyclo[3.2.1]octane-8-carboxylic acid, 3-(hydroxymethyl)-, 1,1-dimethylethyl ester, (3-endo)- is often utilized as a chiral resolving agent and a ligand in asymmetric synthesis. Additionally, it has potential applications in the development of novel drug molecules and could be of interest to researchers in the fields of medicinal chemistry and chemical biology.

Check Digit Verification of cas no

The CAS Registry Mumber 273376-39-9 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 2,7,3,3,7 and 6 respectively; the second part has 2 digits, 3 and 9 respectively.
Calculate Digit Verification of CAS Registry Number 273376-39:
(8*2)+(7*7)+(6*3)+(5*3)+(4*7)+(3*6)+(2*3)+(1*9)=159
159 % 10 = 9
So 273376-39-9 is a valid CAS Registry Number.

273376-39-9SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 19, 2017

Revision Date: Aug 19, 2017

1.Identification

1.1 GHS Product identifier

Product name 1,1-dimethyl-ethyl endo-3-(hydroxymethyl)-8-aza-bicyclo[3.2.1]octane-8-carboxylate

1.2 Other means of identification

Product number -
Other names 1,1-dimethylethyl-(3-endo)-(hydroxymethyl)-8-azabicyclo[3.2.1]octane-8-carboxylate

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:273376-39-9 SDS

273376-39-9Relevant articles and documents

Functional Group Interconversion of Alkylidenemalononitriles to Primary Alcohols by a Cooperative Redox Operation

Emmetiere, Fabien,Grenning, Alexander J.

, p. 3077 - 3085 (2020/08/10)

Functional group interconversions are essential chemical processes enabling synthesis. In this report, we describe a strategy to convert alkylidenemalononitriles into primary alcohols in one step. The reaction relies on a choreographed redox process invol

MUSCARINIC ACETYLCHOLINE RECEPTOR ANTAGONISTS

-

Page/Page column 19-20, (2010/02/15)

Muscarinic Acetylcholine Receptor Antagonists and methods of using them are provided.

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