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(E)-1-phenyl-4-(p-tolyl)but-3-en-1-ol is an organic compound characterized by a conjugated diene system with a phenyl group at the 1-position and a p-tolyl group at the 4-position. This molecule features a double bond between the 2nd and 3rd carbon atoms, which is part of the but-3-en-1-ol structure, indicating a carbon-carbon double bond and a hydroxyl group attached to the 1st carbon. The p-tolyl group, which is a methyl-substituted phenyl group, adds steric hindrance and electronic effects to the molecule. (E)-1-phenyl-4-(p-tolyl)but-3-en-1-ol is likely to be used in organic synthesis, particularly in the preparation of more complex molecules, and may have applications in the pharmaceutical or chemical industries due to its unique structural features.

72004-64-9

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72004-64-9 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 72004-64-9 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 7,2,0,0 and 4 respectively; the second part has 2 digits, 6 and 4 respectively.
Calculate Digit Verification of CAS Registry Number 72004-64:
(7*7)+(6*2)+(5*0)+(4*0)+(3*4)+(2*6)+(1*4)=89
89 % 10 = 9
So 72004-64-9 is a valid CAS Registry Number.

72004-64-9Downstream Products

72004-64-9Relevant academic research and scientific papers

Nickel-catalyzed ring-opening cross-coupling of cyclic alkenyl ethers with arylboronic esters via carbon-oxygen bond cleavage

Ohtsuki, Akimichi,Sakurai, Shun,Tobisu, Mamoru,Chatani, Naoto

supporting information, p. 1277 - 1279 (2016/11/09)

We have developed a nickel-catalyzed cross-coupling reaction of cyclic alkenyl ethers with arylboronic esters that leads to the formation of unsaturated alcohols via ring-opening by the cleavage of a C(sp2)-O bond. The use of 1,3-dicyclohexylimidazol-2-ylidene as the ligand is essential to promote this cross-coupling process.

Chemo-, regio-, and stereoselective Heck-Matsuda arylation of allylic alcohols under mild conditions

Chaudhari, Tohasib Yusub,Hossian, Asik,Manna, Manash Kumar,Jana, Ranjan

supporting information, p. 4841 - 4845 (2015/05/05)

Heck arylation with allylic alcohol is extremely challenging due to chemo-, regio-, and stereoselective scrambling. Here we report a mild protocol for the alcohol selective β- and α-arylation of allylic and cinnamyl alcohols respectively with aryldiazonium salts. The steric and electronic parameters of the alkene play a prominent role in the regioselectivity.

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