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15438-67-2

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15438-67-2 Usage

General Description

Propanamide, 3-methoxy-, also known as N-methyl-N-(3-methoxypropyl) acetamide, is a chemical compound that belongs to the class of amides. It is commonly used in the pharmaceutical industry as a building block in the synthesis of various drugs and pharmaceutical compounds. Its chemical structure contains a propanamide group attached to a 3-methoxypropyl group, making it a versatile compound for use in various chemical reactions and as a precursor for the production of other organic compounds. The 3-methoxypropyl group also contributes to its solubility and stability in various solvents, making it an important ingredient in many pharmaceutical formulations.

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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