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22837-11-2

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22837-11-2 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 22837-11-2 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 2,2,8,3 and 7 respectively; the second part has 2 digits, 1 and 1 respectively.
Calculate Digit Verification of CAS Registry Number 22837-11:
(7*2)+(6*2)+(5*8)+(4*3)+(3*7)+(2*1)+(1*1)=102
102 % 10 = 2
So 22837-11-2 is a valid CAS Registry Number.

22837-11-2Relevant articles and documents

Palladium- and nickel-catalyzed kumada cross-coupling reactions of gem -difluoroalkenes and monofluoroalkenes with Grignard reagents

Dai, Wenpeng,Xiao, Juan,Jin, Guanyi,Wu, Jingjing,Cao, Song

, p. 10537 - 10546 (2015/02/19)

A novel Kumada-Tamao-Corriu cross-coupling reaction of gem-di- or monofluoroalkenes with Grignard reagents, with or without β-hydrogen atoms, in the presence of a catalytic amount of palladium- or nickel-based catalysts has been developed. The reaction is performed under mild conditions (room temperature or reflux in diethyl ether for 1-2 h) and leads to di-cross- or mono-cross-coupled products in good to high yields.

Nickel-catalyzed cross-coupling reaction of alkenyl methyl ethers with aryl boronic esters

Shimasaki, Toshiaki,Konno, Yuko,Tobisu, Mamoru,Chatani, Naoto

supporting information; experimental part, p. 4890 - 4892 (2010/01/06)

The Ni(0)-catalyzed cross-coupling of alkenyl methyl ethers with boronic esters is described. Several types of alkenyl methyl ethers can be coupled with a wide range of boronic esters to give the stilbene derivatives.

Modern Friedel-Crafts Chemistry. Part-XVII. Studies on the Acid-catalysed Dehydration of 3-(α-Naphthylmethyl)-3-pentanol, 2-(α-Naphthyl)-1,1-diphenyl-1-ethanol and 2-Methyl-2-(α-naphthyl)-2-butanol

Khalaf, Ali Ali,Makki, Mohamad S. I. Tawfik,Kaddah, Ahmed M.

, p. 260 - 264 (2007/10/02)

The title α-napthylalkanols were prepared by unequivocal methods and their dehydration patter was examined in the presence of both Lewis and Broensted-Lowry acid-catalysts. 3-(α-Naphthylmethyl)-3-pentanol (5) gave acyclidehydration mixture of 1,1-diethylacenaphthene (10, mainly) and 2-ethyl-1-methyl-2,3-dihydrophenalene (11) with AlCl3/CH3NO2 and an acyclidehydration mixture of 2-methyl-1-(α-naphthyl)-1-butene (12) and Z- and E-3-(α-naphthylmethyl)-2-pentene (13) with 85percent H2SO4, PPA or NaHSO4. 2-(α-Naphthyl)-1,1-diphenyl-1-ethanol (6) gave 1-(α-naphthyl)-2,2-diphenylethene (16) with H2SO4, PPA, NaHSO4 but a different unidentified product with AlCl3/CH3NO2.Finally, 3-methyl-2-(α-naphthyl)-2-butanol (7) gave 1,1,2-trimethyl-acenaphthene (18) with AlCl3/CH3NO2 but 2-methyl-3-(α-naphthyl)-2-butene (19) with 85percent H2SO4 or NaHSO4.Both reactants and products were characterised by elemental, spectral, chemical and glpc analysis.Mechanistic interpretations have been given in terms of carbocation reactions and rearrangements.

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