5468-46-2 Usage
Description
(2Z)-2-cyano-3-(3-nitrophenyl)prop-2-enoic acid, also known as 2-cyano-3-(3-nitrophenyl)acrylic acid, is a compound with the chemical formula C11H8N2O4. It is an unsaturated carboxylic acid that contains a cyanide group and a nitro group. This chemical is commonly used as a starting material for the synthesis of various pharmaceuticals and agrochemicals.
Uses
Used in Pharmaceutical Industry:
(2Z)-2-cyano-3-(3-nitrophenyl)prop-2-enoic acid is used as a starting material for the synthesis of various pharmaceuticals. Its unique chemical structure allows for the development of new drugs with potential therapeutic applications.
Used in Agrochemical Industry:
(2Z)-2-cyano-3-(3-nitrophenyl)prop-2-enoic acid is also used as a starting material for the synthesis of agrochemicals. Its properties make it suitable for the development of new pesticides and other agricultural chemicals.
Used in Chemical Research:
(2Z)-2-cyano-3-(3-nitrophenyl)prop-2-enoic acid has potential applications in the field of chemical research. Its unique structure and reactivity make it a valuable compound for studying various chemical reactions and processes.
It is important to handle (2Z)-2-cyano-3-(3-nitrophenyl)prop-2-enoic acid with care due to its potential toxicity and reactivity. Proper safety measures should be taken to minimize any risks associated with its use.
Check Digit Verification of cas no
The CAS Registry Mumber 5468-46-2 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 5,4,6 and 8 respectively; the second part has 2 digits, 4 and 6 respectively.
Calculate Digit Verification of CAS Registry Number 5468-46:
(6*5)+(5*4)+(4*6)+(3*8)+(2*4)+(1*6)=112
112 % 10 = 2
So 5468-46-2 is a valid CAS Registry Number.
5468-46-2Relevant articles and documents
Preparation method of azelnidipine
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Paragraph 0013, (2017/03/08)
The invention relates to a preparation method of azelnidipine, which comprises the following steps: carrying out Knoevenagel reaction on cyanoacetic acid and m-nitrobenzaldehyde used as starting materials to generate a compound 1; hydrolyzing cyano group of the compound 1 to generate a compound 2; carrying out esterification on the compound 2 and 1-diphenylmethyl-3-azetidin-ol under the action of DCC (N,N'-dicyclohexylcarbodiimide) to generate a compound 3; carrying out Hantzsch cyclization on the compound 3 and isopropyl 3-aminocrotonate under alkaline conditions to generate an azelnidipine crude product; and refining the crude product to obtain the azelnidipine fine product. The method is simple to operate and suitable for industrial production; and the reaction product is easy to separate.
Search for Potential Herbicides. Synthesis of Nitrophenyl-2-cyanoacrylamides
Bhatia, M. S.,Sharma, Sunita,Jindal, Ritu
, p. 162 - 163 (2007/10/02)
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