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96605-66-2

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96605-66-2 Usage

Uses

Different sources of media describe the Uses of 96605-66-2 differently. You can refer to the following data:
1. An impurity and intermediate of Zaleplon production
2. An impurity and intermediate of Zaleplon production.It is used as a reagent in the preparation of immunogens for immunodetection and quantification of pyrazolopyrimidine sedatives.

Check Digit Verification of cas no

The CAS Registry Mumber 96605-66-2 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 9,6,6,0 and 5 respectively; the second part has 2 digits, 6 and 6 respectively.
Calculate Digit Verification of CAS Registry Number 96605-66:
(7*9)+(6*6)+(5*6)+(4*0)+(3*5)+(2*6)+(1*6)=162
162 % 10 = 2
So 96605-66-2 is a valid CAS Registry Number.
InChI:InChI=1/C15H20N2O2/c1-5-17(12(2)18)14-8-6-7-13(11-14)15(19)9-10-16(3)4/h6-11H,5H2,1-4H3/b10-9+

96605-66-2SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 12, 2017

Revision Date: Aug 12, 2017

1.Identification

1.1 GHS Product identifier

Product name N-Ethyl-N-3-((3-Dimethylamino-1-Oxo-2-Propenyl)Phenyl)Acetamide

1.2 Other means of identification

Product number -
Other names N-[3-[(E)-3-(dimethylamino)prop-2-enoyl]phenyl]-N-ethylacetamide

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:96605-66-2 SDS

96605-66-2Relevant articles and documents

A new method for synthesizing zaleplon (by machine translation)

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, (2016/10/10)

The present invention provides a new method for synthesizing zaleplon. In particular, the method of the invention takes the acetophenone as raw materials, make N-ethyl-N-[ 3 - (3- dimethyl amine -1-oxo-2-propenyl) phenyl] acetamide, with 3-amino-4-cyano pyrazole reaction, forming N-[ 3 - (3-cyano-pyrazolo [1,5-α] pyrimidin-7-yl) phenyl]-N-ethyl acetamide. The synthetic route of the present invention of fewer steps, after treatment is simple, low cost, suitable for industrial production. (by machine translation)

2-AMINOPHENYL-4-PHENYLPYRIMIDINES AS KINASE INHIBITORS

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Page/Page column 45-46, (2010/02/10)

The present invention relates to compounds of Formula: (I), or pharmaceutically acceptable salt thereof, wherein the variables are defined in the description. The compounds act as kinase inhibitors.

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