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39096-80-5

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39096-80-5 Usage

General Description

2,2-Dichloro-N-(1-phenylethyl)acetamide is a chemical compound with the molecular formula C10H11Cl2NO. It is used as a topical antifungal and antibacterial agent, often in the form of a cream or ointment. The compound has been shown to be effective in the treatment of various skin infections, including athlete's foot and ringworm. It works by inhibiting the growth of fungi and bacteria on the skin, thereby reducing and eliminating the infection. 2,2-Dichloro-N-(1-phenylethyl)acetamide is considered a safe and effective treatment for these types of infections when used as directed.

Check Digit Verification of cas no

The CAS Registry Mumber 39096-80-5 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 3,9,0,9 and 6 respectively; the second part has 2 digits, 8 and 0 respectively.
Calculate Digit Verification of CAS Registry Number 39096-80:
(7*3)+(6*9)+(5*0)+(4*9)+(3*6)+(2*8)+(1*0)=145
145 % 10 = 5
So 39096-80-5 is a valid CAS Registry Number.

39096-80-5SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 19, 2017

Revision Date: Aug 19, 2017

1.Identification

1.1 GHS Product identifier

Product name 2,2-Dichloro-N-(1-phenylethyl)acetamide

1.2 Other means of identification

Product number -
Other names 2,2-DIBROMO-3-OXO-BUTYRIC ACID ETHYL ESTER

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:39096-80-5 SDS

39096-80-5Relevant articles and documents

Stereoselective synthesis of racemic α-amino-acid derivatives with a β-lactam skeleton: Application of the Staudinger reaction to chiral imines of methyl glyoxylate

Barreau, Michel,Commercon, Alain,Mignani, Serge,Mouysset, Dominique,Perfetti, Patricia,Stella, Lucien

, p. 11501 - 11516 (2007/10/03)

Selected imines of methyl glyoxylate act as good partners in the Staudinger cycloaddition reaction with a series of substituted ketenes. The cis stereoselectivity is almost complete with electron-donor substituted ketenes, but the asymmetric induction is low when imines derived from chiral l-aryl-ethylamines are used.

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