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2-Amino-1-(4-nitrophenyl)ethan-1-one hydrochloride hydrate is an organic chemical compound composed of hydrogen, chlorine, nitrogen, oxygen, and carbon atoms. It is characterized by a molar mass of 232.64 g/mol, a melting point of 208-210 °C, and a boiling point of 401.2 °C. 2-AMINO-1-(4-NITROPHENYL)ETHAN-1-ONE HYDROCHLORIDE HYDRATE appears as a yellow crystalline powder and is soluble in water. Due to its potential hazard as an irritant to eyes, skin, and respiratory system, it requires careful handling.

4740-22-1

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4740-22-1 Usage

Uses

Used in Scientific Research:
2-Amino-1-(4-nitrophenyl)ethan-1-one hydrochloride hydrate is used as a reagent or precursor in various chemical reactions for scientific research purposes. Its unique properties and reactivity make it a valuable component in the development and synthesis of new compounds and materials.

Check Digit Verification of cas no

The CAS Registry Mumber 4740-22-1 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 4,7,4 and 0 respectively; the second part has 2 digits, 2 and 2 respectively.
Calculate Digit Verification of CAS Registry Number 4740-22:
(6*4)+(5*7)+(4*4)+(3*0)+(2*2)+(1*2)=81
81 % 10 = 1
So 4740-22-1 is a valid CAS Registry Number.
InChI:InChI=1/C8H8N2O3.ClH.H2O/c9-5-8(11)6-1-3-7(4-2-6)10(12)13;;/h1-4H,5,9H2;1H;1H2

4740-22-1SDS

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 2-amino-1-(4-nitrophenyl)ethanone,hydrate,hydrochloride

1.2 Other means of identification

Product number -
Other names 4-Nitrophenacylamine hydrochloride hydrate

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:4740-22-1 SDS

4740-22-1Relevant academic research and scientific papers

TBAI-catalyzed oxidative cross-coupling of phenols and 2-aminoacetophenones

Xu, Wei,Nachtsheim, Boris J.

supporting information, p. 1585 - 1588 (2015/03/30)

An iodide-catalyzed oxidative cross-coupling between phenols and 2-aminoacetophenones has been developed. Using catalytic amounts of tetrabutylammoniumiodide (TBAI) as an iodine-containing catalyst and aqueous solutions of tert-butyl hydro-peroxide (TBHP)

Evaluation of thiazole containing biaryl analogs as diacylglycerol acyltransferase 1 (DGAT1) inhibitors

Kadam, Kishorkumar S.,Jadhav, Ravindra D.,Kandre, Shivaji,Guha, Tandra,Reddy, M. Mahesh Kumar,Brahma, Manoja K.,Deshmukh, Nitin J.,Dixit, Amol,Doshi, Lalit,Srinivasan, Shaila,Devle, Jayendra,Damre, Anagha,Nemmani, Kumar V. S.,Gupte, Amol,Sharma, Rajiv

, p. 337 - 347 (2013/10/01)

Biphenyl carboxylic acids, exemplified by compound 5, are known potent inhibitors of diacylglycerol acyltransferase, DGAT1, an enzyme involved in the final committed step of triglyceride biosynthesis. We have synthesized and evaluated 2-phenylthiazole, 4-

1-[[[5-(Substituted phenyl)-2-oxazolyl]methylene]amino]-2,4-imidazolidinediones

-

, (2008/06/13)

A series of 1-[[[5-(substituted phenyl-2-oxazolyl]methylene]amino]-2,4-imidazolidinediones are useful as muscle relaxants.

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