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4-(acetylamino)-3-aminophenyl acetate, commonly known as paracetamol or acetaminophen, is a nonsteroidal anti-inflammatory drug (NSAID) that is widely used as a pain reliever and fever reducer. It is a white, crystalline powder that is typically administered orally. Paracetamol works by inhibiting the production of prostaglandins in the brain, which are responsible for transmitting pain signals.

7474-93-3

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7474-93-3 Usage

Uses

Used in Pharmaceutical Industry:
4-(acetylamino)-3-aminophenyl acetate is used as a pain reliever and fever reducer for treating a variety of conditions such as headaches, muscle aches, arthritis, and fevers. It is considered safe when taken in recommended doses, but can cause liver damage if taken in excess.

Check Digit Verification of cas no

The CAS Registry Mumber 7474-93-3 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 7,4,7 and 4 respectively; the second part has 2 digits, 9 and 3 respectively.
Calculate Digit Verification of CAS Registry Number 7474-93:
(6*7)+(5*4)+(4*7)+(3*4)+(2*9)+(1*3)=123
123 % 10 = 3
So 7474-93-3 is a valid CAS Registry Number.

7474-93-3SDS

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 (4-acetamido-3-aminophenyl) acetate

1.2 Other means of identification

Product number -
Other names 5-acetoxy-2-acetylamino-aniline

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:7474-93-3 SDS

7474-93-3Relevant academic research and scientific papers

Acylamino-Directed Specific Sequential Difunctionalizations of Anilides via Metal-Free Relay Reactions for p-Oxygen and o-Nitrogen Incorporation

Wan, Yameng,Zhang, Zhiguo,Ma, Nana,Bi, Jingjing,Zhang, Guisheng

, p. 780 - 791 (2019/01/24)

Novel acylamino-directed relay disubstitutions realize the sequential difunctionalizations of anilides (1) under mild and metal-free conditions for the first time. This [bis(trifluoroacetoxy)iodo]benzene (PIFA) and BF3·Et2O promoted straightforward reaction produces a series of p-acetoxyl- or p-alkoxyl-o-nitro-N-arylamides (2), which are key scaffolds of various drugs, functional materials, and bioactive molecules. The flexibility with respect to the functional groups in these products affords this novel protocol excellent versatility for synthetic applications.

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