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2-[(3,4-dichlorophenyl)amino]-2-ethoxy-1-phenylethanone is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

79866-29-8

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79866-29-8 Usage

Appearance

Yellowish crystalline solid

Use as a sympathomimetic agent

Treatment of hypotension and as a bronchodilator

Mechanism of action

Stimulates alpha and beta adrenergic receptors, leading to vasoconstriction and increased heart rate

Application in synthesis

Used in the synthesis of other organic compounds

Potential applications

Chemical research and pharmaceutical development

Precautions

Handle with care due to potential health hazards and environmental risks

Check Digit Verification of cas no

The CAS Registry Mumber 79866-29-8 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 7,9,8,6 and 6 respectively; the second part has 2 digits, 2 and 9 respectively.
Calculate Digit Verification of CAS Registry Number 79866-29:
(7*7)+(6*9)+(5*8)+(4*6)+(3*6)+(2*2)+(1*9)=198
198 % 10 = 8
So 79866-29-8 is a valid CAS Registry Number.

79866-29-8SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 17, 2017

Revision Date: Aug 17, 2017

1.Identification

1.1 GHS Product identifier

Product name 2-(3,4-dichloroanilino)-2-ethoxy-1-phenylethanone

1.2 Other means of identification

Product number -
Other names -

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:79866-29-8 SDS

79866-29-8Downstream Products

79866-29-8Relevant academic research and scientific papers

Removal of Toluene-p-sulphonyl Groups from Sulphonamides. Part 4. Synthesis of Phenylglyoxal Imine Monomers

McKay, William R.,Proctor, George R.

, p. 2435 - 2442 (2007/10/02)

Syntheses and reactions of N-tosylphenacylamines with bases have been systematically examined.Monomeric C-methoxy-imines are available from some of these reactions.C-Methoxyphenacylarylamines, made by two routes, were converted into monomeric imines on treatment with noble-metal catalysts, The boron trifluoride-catalysed reactions of aryl aldehydes with sulphonamides provide a new and convenient route to N-sulphonylarylimines.

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