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54903-55-8

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54903-55-8 Usage

General Description

The chemical (4-amino-3-hydroxyphenyl)(thiophen-2-yl)methanone, also known as AHPTM, is a compound with both amino and hydroxy functional groups attached to a phenyl ring, as well as a thiophen-2-yl group attached to a methanone moiety. (4-amino-3-hydroxyphenyl)(thiophen-2-yl)methanone is of interest in the field of medicinal chemistry, as it has shown potential for various biological activities, including anti-inflammatory and antineoplastic properties. Additionally, it has been the subject of research for its potential use in the development of pharmaceutical drugs. Its unique structure makes it a candidate for further investigation and potential therapeutic applications.

Check Digit Verification of cas no

The CAS Registry Mumber 54903-55-8 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 5,4,9,0 and 3 respectively; the second part has 2 digits, 5 and 5 respectively.
Calculate Digit Verification of CAS Registry Number 54903-55:
(7*5)+(6*4)+(5*9)+(4*0)+(3*3)+(2*5)+(1*5)=128
128 % 10 = 8
So 54903-55-8 is a valid CAS Registry Number.

54903-55-8SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 13, 2017

Revision Date: Aug 13, 2017

1.Identification

1.1 GHS Product identifier

Product name (4-amino-3-hydroxyphenyl)-thiophen-2-ylmethanone

1.2 Other means of identification

Product number -
Other names JPB 20

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:54903-55-8 SDS

54903-55-8Downstream Products

54903-55-8Relevant articles and documents

Unequivocal Preparation of 4- and 5-Acyl-2-aminophenols

Aichaoui, Hocine,Lesieur, Isabelle,Henichart, Jean-Pierre

, p. 679 - 680 (2007/10/02)

Unequivocal methods for the specific preparation of 4- or 5-acyl-2-aminophenols are reported. 5-Acyl-2-aminophenols are obtained by ring opening with dilute sodium hydroxide of 2(3H)-benzoxazolinones acylated at position 6. 4-Acyl-2-aminophenols are obtai

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