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5-Methoxy-2-(1-phenylallyl)phenol is a complex organic compound with the molecular formula C17H16O2. It is characterized by a phenol group (C6H5OH) with a methoxy (-OCH3) substituent at the 5th position and a 1-phenylallyl group attached to the 2nd position. The 1-phenylallyl group consists of a phenyl ring (C6H5) and an allyl chain (CH2=CH-CH2). 5-methoxy-2-(1-phenylallyl)phenol is known for its potential applications in the synthesis of various pharmaceuticals and agrochemicals due to its unique structure and reactivity. It is also used as an intermediate in the production of certain dyes and pigments. The compound's properties, such as its solubility and stability, can be influenced by the presence of the methoxy and phenylallyl groups, making it a versatile building block in organic chemistry.

4647-01-2

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4647-01-2 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 4647-01-2 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 4,6,4 and 7 respectively; the second part has 2 digits, 0 and 1 respectively.
Calculate Digit Verification of CAS Registry Number 4647-01:
(6*4)+(5*6)+(4*4)+(3*7)+(2*0)+(1*1)=92
92 % 10 = 2
So 4647-01-2 is a valid CAS Registry Number.

4647-01-2Relevant academic research and scientific papers

Ring-closing metathesis as a new methodology for the synthesis of monomeric flavonoids and neoflavonoids

Miller, Bradley J.,Pieterse, Tanya,Marais, Charlene,Bezuidenhoudt, Barend C.B.

, p. 4708 - 4710 (2012/09/21)

Basic flavonoid (flavene) and neoflavonoid (neoflavene) skeletons were successfully synthesized using ring-closing metathesis, showing that this methodology can be used as a central synthetic tool for the synthesis of at least two of the three basic flavonoid classes.

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