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142713-08-4

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142713-08-4 Usage

General Description

Acetamide, 2-(diethylamino)-N-(2,3-dimethylphenyl)- is a chemical compound with the molecular formula C14H22N2O. It is a derivative of acetamide with diethylamino and 2,3-dimethylphenyl substituents. Acetamide, 2-(diethylamino)-N-(2,3-dimethylphenyl)- is commonly found as a pharmaceutical intermediate and may exhibit properties that make it useful in the development of pharmaceutical drugs. Its precise applications and potential effects may vary based on the specific industry or context in which it is used.

Check Digit Verification of cas no

The CAS Registry Mumber 142713-08-4 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,4,2,7,1 and 3 respectively; the second part has 2 digits, 0 and 8 respectively.
Calculate Digit Verification of CAS Registry Number 142713-08:
(8*1)+(7*4)+(6*2)+(5*7)+(4*1)+(3*3)+(2*0)+(1*8)=104
104 % 10 = 4
So 142713-08-4 is a valid CAS Registry Number.

142713-08-4SDS

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-(diethylamino)-N-(2,3-dimethylphenyl)acetamide

1.2 Other means of identification

Product number -
Other names 2-Diethylamino-2',3'-acetoxylidide

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:142713-08-4 SDS

142713-08-4Downstream Products

142713-08-4Relevant articles and documents

Synthesis and antispasmodic activity of lidocaine derivatives endowed with reduced local anesthetic action

Costa, Jorge C.S.,Neves, Josiane S.,de Souza, Marcus V.N.,Siqueira, Rodrigo A.,Romeiro, Nelilma C.,Boechat, Nubia,Silva, Patricia M.R.e,Martins, Marco A.

, p. 1162 - 1166 (2008/09/20)

The present structure-activity relationship (SAR) study focused on chemical modifications of the structure of the local anesthetic lidocaine, and indicated analogues having reduced anesthetic potency, but with superior potency relative to the prototype in preventing anaphylactic or histamine-evoked ileum contraction. From the SAR analysis, 2-(diethylamino)-N-(trifluoromethyl-phenyl) and 2-(diethylamino)-N-(dimethyl-phenyl) acetamides were selected as the most promising compounds. New insights into the applicability of non-anesthetic lidocaine derivatives as templates in drug discovery for allergic syndromes are provided.

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