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Benzenemethanol, 4-(2-benzofuranyl)-, also known as 4-(2-Benzofuranyl)benzenemethanol or 4-(2-Benzofuranylmethyl)benzyl alcohol, is an organic compound with the chemical formula C14H12O2. It is a colorless to pale yellow liquid with a molecular weight of 212.24 g/mol. Benzenemethanol, 4-(2-benzofuranyl)- is characterized by the presence of a benzyl alcohol group (C6H5CH2OH) and a benzofuran moiety (C6H4O), which is a heterocyclic aromatic ring system consisting of a benzene ring fused to a furan ring. Benzenemethanol, 4-(2-benzofuranyl)-, is used as an intermediate in the synthesis of various pharmaceuticals, agrochemicals, and other specialty chemicals due to its unique structural features and potential reactivity.

36079-00-2

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36079-00-2 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 36079-00-2 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 3,6,0,7 and 9 respectively; the second part has 2 digits, 0 and 0 respectively.
Calculate Digit Verification of CAS Registry Number 36079-00:
(7*3)+(6*6)+(5*0)+(4*7)+(3*9)+(2*0)+(1*0)=112
112 % 10 = 2
So 36079-00-2 is a valid CAS Registry Number.

36079-00-2Relevant academic research and scientific papers

Microwave-assisted Suzuki coupling reactions with an encapsulated palladium catalyst for batch and continuous-flow transformations

Baxendale, Ian R.,Griffiths-Jones, Charlotte M.,Ley, Steven V.,Tranmer, Geoffrey K.

, p. 4407 - 4416 (2006)

This article describes the design, optimisation and development of a Suzuki cross-coupling protocol mediated by an efficient palladium-en-capsulated catalyst (Pd EnCat) under microwave irradiation. The methodology has been used in both batch mode for classical library preparation and in continuous-flow applications furnishing multigram quantities of material. Described is a method that uses direct focused microwave heating whilst applying an external cooling source. This enables a lower than normal bulk temperature to be maintained throughout the reaction period leading to significant improvements in the overall yield and purity of the reaction products. Additional aspects of this novel heating protocol are discussed in relation to the prolonged lifetime and enhanced reactivity of the immobilised catalyst system.

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