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90874-60-5

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90874-60-5 Usage

General Description

2-Amino-3',4'-Dimethyl-Acetophenone Hydrochloride is a compound that is used in the synthesis of pharmaceuticals and organic compounds. It is a derivative of acetophenone, a versatile building block in organic chemistry. The addition of an amino group and two methyl groups to the acetophenone molecule adds new functionality and reactivity, making it valuable in the production of various compounds. The hydrochloride salt form of this chemical makes it water soluble, which is useful in many applications. It is also commonly used as a building block for the synthesis of heterocyclic compounds, which have a wide range of potential biological activities.

Check Digit Verification of cas no

The CAS Registry Mumber 90874-60-5 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 9,0,8,7 and 4 respectively; the second part has 2 digits, 6 and 0 respectively.
Calculate Digit Verification of CAS Registry Number 90874-60:
(7*9)+(6*0)+(5*8)+(4*7)+(3*4)+(2*6)+(1*0)=155
155 % 10 = 5
So 90874-60-5 is a valid CAS Registry Number.

90874-60-5SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 15, 2017

Revision Date: Aug 15, 2017

1.Identification

1.1 GHS Product identifier

Product name 2-Amino-1-(3,4-dimethylphenyl)ethanone

1.2 Other means of identification

Product number -
Other names 2-amino-1-(3,4-dimethylphenyl)ethan-1-one

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:90874-60-5 SDS

90874-60-5Downstream Products

90874-60-5Relevant articles and documents

A Convenient Synthesis of Aminomethyl Ketones (α-Amino Ketones)

Yinglin, Han,Hongwen, Hu

, p. 615 - 618 (2007/10/02)

Several N,N-diformylaminomethyl ketones 3 were prepared by treating the respective bromomethylketone 1 with sodium diformylamide in acetonitrile at room temperature.This reaction produced from N-formylaminomethyl ketones 4 when ethanol was used as the solvent.One of the formyl groups of N,N-difomylaminomethyl ketones was selectively removed by using a catalytic amount of sodium or potassium hydroxide in alcohol to the corresponding N-formylaminomethyl ketones 4.The formyl groups of both N,N-diformyl- and N-formylaminomethyl ketones could be easily removed by either5percent hydrochloric acid in ethanol or 6N hydrochloric acid to give the corresponding aminomethyl ketone hydrochlorides 5.These reactions are general and give high yield of the products.

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