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500288-66-4

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500288-66-4 Usage

Type of Compound

Propenamide

Chemical Structure

Contains a carbon-carbon double bond and an amide functional group

Functional Groups

Aromatic rings
Amino groups

Configuration

(2E) designation indicates cis configuration with respect to the double bond

Potential Applications

Chemical synthesis
Pharmaceutical applications

Interest for Further Study

Unique arrangement and functional groups make it suitable for research and potential applications in various fields

Check Digit Verification of cas no

The CAS Registry Mumber 500288-66-4 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 5,0,0,2,8 and 8 respectively; the second part has 2 digits, 6 and 6 respectively.
Calculate Digit Verification of CAS Registry Number 500288-66:
(8*5)+(7*0)+(6*0)+(5*2)+(4*8)+(3*8)+(2*6)+(1*6)=124
124 % 10 = 4
So 500288-66-4 is a valid CAS Registry Number.

500288-66-4Downstream Products

500288-66-4Relevant articles and documents

Method for preparing high-purity ribavirin intermediate by one-pot method (by machine translation)

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Paragraph 0014; 0051-0052; 0054-0061; 0063-0066, (2020/12/14)

The invention relates to the technical field of chemical medicine, in particular to a method for preparing a high-purity ribavirin intermediate by a one-pot method. The method comprises the following steps: (1) replacing the compound I with the compound II to obtain the reaction liquid of the compound III. (2) Acrylamide was added to III reaction liquid of the compound, and the reaction liquid of compound IV was obtained under Heck reaction conditions. (3) In the reaction solution of Compound IV, activated carbon is first added for decolorization treatment, and then a poor solvent is added for crystallization to obtain a white compound IV, i.e. a ripe intermediate. The method for preparing the high-purity ribavirin intermediate by one-pot method is scientific, reasonable, simple and feasible, improves product purity and yield, and is suitable for large-scale production. (by machine translation)

PROCESSES FOR THE PREPARATION OF 4-[[4-[[4-(2-CYANOETHENYL)-2,6-DIMETHYLPHENYL]AMINO]-2-PYRIMIDINYL]AMINO]BENZONITRILE

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Page 23, (2008/06/13)

Processes for the preparation of 4-[[4-[[4-(2-cyanoethenyl)-2,6-dimethylphenyl]amino]-2-pyrimidinyl]amino]benzonitrile of formula (I), a N-oxide, a pharmaceutically acceptable acid addition salt, a quaternary amine or a stereochemically isomeric form thereof are provided, said processes comprise a) reacting 4-(2-cyanoethenyl)-2,6-dimethylbenzenamine with an intermediate of formula (III) in the presence of a suitable solvent; b) reacting an intermediate of formula (IV) with acrylonitrile in the presence of a suitable palladium catalyst, a suitable base and a suitable solvent; c) dehydrating the corresponding amide of the compound of formula (I).

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