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15438-67-2

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15438-67-2 Usage

Description

Propanamide, 3-methoxy-, also known as N-methyl-N-(3-methoxypropyl) acetamide, is a versatile chemical compound belonging to the class of amides. It features a propanamide group attached to a 3-methoxypropyl group, which enhances its solubility and stability in various solvents. This makes it a valuable building block in the pharmaceutical industry for the synthesis of a wide range of drugs and pharmaceutical compounds.

Uses

Used in Pharmaceutical Industry:
Propanamide, 3-methoxyis used as a building block for the synthesis of various drugs and pharmaceutical compounds due to its versatile chemical structure and compatibility with different chemical reactions.
Used in Chemical Reactions:
Propanamide, 3-methoxyis used as a precursor for the production of other organic compounds, leveraging its unique structure and reactivity in various chemical processes.
Used in Pharmaceutical Formulations:
Propanamide, 3-methoxyis used as an important ingredient in many pharmaceutical formulations, contributing to the solubility and stability of the final products in different solvents.

Check Digit Verification of cas no

The CAS Registry Mumber 15438-67-2 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 1,5,4,3 and 8 respectively; the second part has 2 digits, 6 and 7 respectively.
Calculate Digit Verification of CAS Registry Number 15438-67:
(7*1)+(6*5)+(5*4)+(4*3)+(3*8)+(2*6)+(1*7)=112
112 % 10 = 2
So 15438-67-2 is a valid CAS Registry Number.

15438-67-2SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 12, 2017

Revision Date: Aug 12, 2017

1.Identification

1.1 GHS Product identifier

Product name 3-methoxypropanamide

1.2 Other means of identification

Product number -
Other names Propanamide,3-methoxy

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:15438-67-2 SDS

15438-67-2Relevant articles and documents

Dabi,Zilkha

, p. 545,551 (1977)

Method for converting amides to nitriles and nitriles to amides

-

, (2008/06/13)

A process which comprises contacting and catalytically reacting under essentially anhydrous conditions in the liquid phase an amide with a nitrile according to the equation: where R and R1 are not the same and are each selected from (1) H, hydrocarbyl, a hydrocarbyl group substituted with: one or more of F, Cl, Br, I, amido, cyano, formyl, hydrocarbylcarbonyl, hydrocarbyloxy, hydrocarbyloxycarbonyl, hydrocarbylcarbonyloxy and dihydrocarbylamino, and (2) any of group (1) where one or more H atoms are substituted by a deuterium atom,

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