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1-(4-amino-3-hydroxyphenyl)propan-1-one is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

54903-52-5

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54903-52-5 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 54903-52-5 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 2 respectively.
Calculate Digit Verification of CAS Registry Number 54903-52:
(7*5)+(6*4)+(5*9)+(4*0)+(3*3)+(2*5)+(1*2)=125
125 % 10 = 5
So 54903-52-5 is a valid CAS Registry Number.

54903-52-5SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 13, 2017

Revision Date: Aug 13, 2017

1.Identification

1.1 GHS Product identifier

Product name 1-(4-amino-3-hydroxyphenyl)propan-1-one

1.2 Other means of identification

Product number -
Other names JPB 16

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:54903-52-5 SDS

54903-52-5Relevant academic research and scientific papers

Discovery and optimization of novel fatty acid transport protein 1 (FATP1) inhibitors

Matsufuji, Tetsuyoshi,Ikeda, Mika,Naito, Asuka,Hirouchi, Masakazu,Takakusa, Hideo,Kanda, Shoichi,Izumi, Masanori,Harada, Jun,Shinozuka, Tsuyoshi

scheme or table, p. 5067 - 5070 (2012/09/07)

The discovery, optimization and structure-activity relationship of novel FATP1 inhibitors have been described. The detailed SAR studies of each moiety of the inhibitors combined with metabolite analysis led to the identification of the potent inhibitors 1

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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