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α-(4-chloro-benzoylamino)-trans-cinnamic acid is a synthetic chemical compound with the molecular formula C16H13ClNO3. It is a derivative of cinnamic acid, featuring a 4-chloro-benzoyl group attached to the α-amino group. α-(4-chloro-benzoylamino)-trans-cinnamic acid is known for its potential applications in the pharmaceutical industry, particularly as an intermediate in the synthesis of various drugs and agrochemicals. Its trans configuration indicates that the double bond in the cinnamic acid moiety is in the E-geometry, which can influence its physical and chemical properties. The presence of the chlorine atom in the benzoyl group may also affect its reactivity and stability, making it a compound of interest for further chemical modifications and research.

59490-25-4

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59490-25-4 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 59490-25-4 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 5,9,4,9 and 0 respectively; the second part has 2 digits, 2 and 5 respectively.
Calculate Digit Verification of CAS Registry Number 59490-25:
(7*5)+(6*9)+(5*4)+(4*9)+(3*0)+(2*2)+(1*5)=154
154 % 10 = 4
So 59490-25-4 is a valid CAS Registry Number.

59490-25-4Relevant academic research and scientific papers

Synthesis of oxazoles from enamides via phenyliodine diacetate-mediated intramolecular oxidative cyclization

Zheng, Yunhui,Li, Xuming,Ren, Chengfeng,Zhang-Negrerie, Daisy,Du, Yunfei,Zhao, Kang

, p. 10353 - 10361 (2013/01/15)

A group of functionalized oxazoles were synthesized in moderate to good yields from enamides via phenyliodine diacetate (PIDA)-mediated intramolecular cyclization. The main advantageous features of the present method include its broad substrate scope and the heavy-metal-free characteristic of the oxidative carbon-oxygen bond formation process.

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