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3-Methoxy-3-methylazetidine, a heterocyclic organic compound with the molecular formula C6H13NO, features a four-membered ring containing both an oxygen and a nitrogen atom. It is widely recognized for its versatility in forming various chemical bonds and functional groups, making it a valuable building block in the synthesis of pharmaceuticals, agrochemicals, and materials. Its potential in medicinal chemistry for the development of new drugs for diverse therapeutic purposes further underscores its significance in the field of research and industrial applications.

877665-31-1

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877665-31-1 Usage

Uses

Used in Pharmaceutical Synthesis:
3-Methoxy-3-methylazetidine is utilized as a key building block in the creation of pharmaceuticals, contributing to the development of novel drugs for a range of therapeutic applications. Its unique structure and ability to form multiple chemical bonds make it an indispensable component in the synthesis of complex molecules.
Used in Agrochemical Development:
In the agrochemical industry, 3-Methoxy-3-methylazetidine serves as a crucial intermediate in the synthesis of various agrochemicals, including pesticides and herbicides. Its role in creating effective and environmentally friendly products is vital for agricultural productivity and sustainability.
Used in Material Science:
3-Methoxy-3-methylazetidine is employed as a reagent in material science, where it aids in the synthesis of advanced materials with specific properties. Its versatility in forming functional groups allows for the development of materials with tailored characteristics for use in various applications, such as coatings, adhesives, and polymers.
Used in Organic Synthesis as a Reagent:
3-Methoxy-3-methylazetidine is used as a reagent in organic synthesis due to its capacity to form a variety of chemical bonds and functional groups. This makes it a valuable tool for chemists in creating new organic compounds and exploring novel chemical reactions.
Used in Medicinal Chemistry for Drug Development:
3-Methoxy-3-methylazetidine holds promise in medicinal chemistry, particularly in the development of new drugs for various therapeutic purposes. Its unique structural features and reactivity make it a candidate for the design and synthesis of innovative pharmaceutical agents targeting different medical conditions.

Check Digit Verification of cas no

The CAS Registry Mumber 877665-31-1 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 8,7,7,6,6 and 5 respectively; the second part has 2 digits, 3 and 1 respectively.
Calculate Digit Verification of CAS Registry Number 877665-31:
(8*8)+(7*7)+(6*7)+(5*6)+(4*6)+(3*5)+(2*3)+(1*1)=231
231 % 10 = 1
So 877665-31-1 is a valid CAS Registry Number.

877665-31-1SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 18, 2017

Revision Date: Aug 18, 2017

1.Identification

1.1 GHS Product identifier

Product name 3-Methoxy-3-methylazetidine

1.2 Other means of identification

Product number -
Other names 3-methoxy-3-methylazetidine

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:877665-31-1 SDS

877665-31-1Downstream Products

877665-31-1Relevant academic research and scientific papers

As the NS4B inhibitor benzofuran analogs (by machine translation)

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Paragraph 0394; 0396; 0397; 0400; 03401, (2016/10/31)

The present invention discloses a kind of as NS4B benzofuran analogue inhibitors, in particular to the formula (I) below or a pharmaceutically acceptable salt thereof. (by machine translation)

ENANTIOPURE PHARMACOLOGICALLY ACTIVE TRICYCLIC BENZIMIDAZOLES

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Page/Page column 80, (2008/12/08)

The invention provides compounds of the formula (1) in which the substituents and symbols are as de fined in the description. The compounds inhibit the secretion of gastric acid.

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