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3-(2-ethylphenyl)prop-2-yl-1-ol is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

862074-52-0

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862074-52-0 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 862074-52-0 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 8,6,2,0,7 and 4 respectively; the second part has 2 digits, 5 and 2 respectively.
Calculate Digit Verification of CAS Registry Number 862074-52:
(8*8)+(7*6)+(6*2)+(5*0)+(4*7)+(3*4)+(2*5)+(1*2)=170
170 % 10 = 0
So 862074-52-0 is a valid CAS Registry Number.

862074-52-0Relevant academic research and scientific papers

Catalyst-Free Annulation of 2-Pyridylacetates and Ynals with Molecular Oxygen: An Access to 3-Acylated Indolizines

Chen, Zhengwang,Liang, Pei,Ma, Xiaoyue,Luo, Haiqing,Xu, Guohai,Liu, Tanggao,Wen, Xiaowei,Zheng, Jing,Ye, Hui

supporting information, p. 1630 - 1639 (2019/01/26)

A catalyst and additive-free annulation of 2-pyridylacetates and ynals under molecular oxygen was the first developed, affording 3-acylated indolizines in good to excellent yields. Molecular oxygen was used as the source of the carbonyl oxygen atom in indolizines. This approach was compatible with a wide range of functional groups, and especially it has been successfully extended to unsaturated double bonds and triple bonds, which were difficult to prepare by previous methods in a single step.

Synthesis of 3-benzylisoquinolines by domino imination/cycloisomerisation of 2-propargylbenzaldehydes

Dell'Acqua, Monica,Pirovano, Valentina,Confalonieri, Giorgio,Arcadi, Antonio,Rossi, Elisabetta,Abbiati, Giorgio

, p. 8019 - 8030 (2015/01/08)

An easy entry to uncommon 2-propargylbenzaldehydes was developed. 2-Propargylbenzaldehydes demonstrated to be suitable building blocks for the synthesis of 3-benzyl isoquinolines by microwave promoted domino imination/cycloisomerisation in the presence of

Gold-catalyzed annulation/fragmentation: Formation of free gold carbenes by retro-cyclopropanation

Solorio-Alvarado, Cesar R.,Echavarren, Antonio M.

supporting information; experimental part, p. 11881 - 11883 (2010/10/19)

The gold(I)-catalyzed cyclization of 1-(prop-2-yn-1-yl)-2-alkenylbenzenes substituted at the benzylic position with OR groups gives 1,3-disubstituted naphthalenes with concomitant fragmentation of the alkene. One of these annulations proceeds by a retro-cyclopropanation that leads to free gold(I) carbenes.

Enantioselective synthesis of axially chiral biaryls through rhodium-catalyzed complete intermolecular cross-cyclotrimerization of internal alkynes

Tanaka, Ken,Nishida, Goushi,Ogino, Masakazu,Hirano, Masao,Noguchi, Keiichi

, p. 3119 - 3121 (2007/10/03)

(Chemical Equation Presented) We have developed a cationic rhodium(I)/H8-BINAP complex-catalyzed complete intermolecular cross-cyclotrimerization of internal alkynes with dialkyl acetylenedicarboxylates. This reaction was successfully applied to enantiose

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