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(Z)-2-benzoylamino-3-(4-methoxyphenyl)prop-2-enamide is a complex organic chemical compound with the molecular formula C17H16N2O3. It is a derivative of cinnamic acid, featuring a benzoyl group attached to the amino group, and a 4-methoxyphenyl group on the third carbon. (Z)-2-benzoylamino-3-(4-methoxyphenyl)prop-2-enamide is characterized by its Z-configuration, indicating the geometric arrangement of the double bond, with the benzoyl and 4-methoxyphenyl groups on the same side of the molecule. It is a white crystalline solid and is known for its potential applications in pharmaceuticals, particularly as an intermediate in the synthesis of various drugs and bioactive molecules. The compound's structure and properties make it a subject of interest in organic chemistry and medicinal chemistry research.

70985-02-3

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70985-02-3 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 70985-02-3 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 7,0,9,8 and 5 respectively; the second part has 2 digits, 0 and 2 respectively.
Calculate Digit Verification of CAS Registry Number 70985-02:
(7*7)+(6*0)+(5*9)+(4*8)+(3*5)+(2*0)+(1*2)=143
143 % 10 = 3
So 70985-02-3 is a valid CAS Registry Number.

70985-02-3Relevant academic research and scientific papers

A practical and efficient synthesis of 2,5-disubstituted-3,5-dihydro- imidazol-4-ones from oxazolones

Chavez, Flavio,Pavy, Caslin,Williamson, Thomas,Cleary, Thomas

experimental part, p. 3321 - 3327 (2012/09/21)

An alternative procedure for the synthesis of 2,5-disubstituted-3,5- dihydro-imidazol-4-ones from substituted oxazolones was evaluated. The initial oxazolone ring-opening reaction was examined with a variety of ammonia source compounds followed by the sub

Derivatives of α,β-dehydro amino acids: III. Reaction of 4-arylmethylidene-4,5-dihydro-1,3-oxazol-5-ones with hexamethyldisilazane

Topuzyan,Arutyunyan,Oganesyan

, p. 868 - 871 (2008/03/11)

4-Arylmethylidene-4,5-dihydro-1,3-oxazol-5-ones reacted with hexamethyldisilazane in ethyl acetate, acetonitrile, or DMF at room temperature to give mainly 2-acylamino-3-arylmethylideneprop-2-enamides, whereas in boiling DMF the corresponding 4-arylmethyl

A new methodology for the synthesis of N-acylaminocinnamates

Rao, Ch. Chennakesava,Lalitha, Nagubandi

, p. 3 (2007/10/02)

A new synthesis of biologically active N-protected amino acids (2) and amides (4) from 4-ylidene-5(4H)-oxazolones (1) is described.

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