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2,3'-Biquinoline, 1',2'-dihydro-1'-methyl-2'-phenyl- is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

263396-32-3

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263396-32-3 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 263396-32-3 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 2,6,3,3,9 and 6 respectively; the second part has 2 digits, 3 and 2 respectively.
Calculate Digit Verification of CAS Registry Number 263396-32:
(8*2)+(7*6)+(6*3)+(5*3)+(4*9)+(3*6)+(2*3)+(1*2)=153
153 % 10 = 3
So 263396-32-3 is a valid CAS Registry Number.

263396-32-3Downstream Products

263396-32-3Relevant academic research and scientific papers

Investigations on 2,3′-biquinoline series. 19. Regioselectivity of the reaction of 1,1′-dialkyl-3,3′-di(2-quinolyl)-1,1′,4, 4′-tetrahydro-4,4′-biquinolines with organomagnesium and organolithium compounds

Antonova,Goncharov,Aksenov

, p. 197 - 199 (2006)

1,1′-Dialkyl-3,3′-di(2-quinolyl)-1,1′,4, 4′-tetrahydro-4,4′-biquinolines react with organolithium and organo-magnesium compounds to form 1′-alkyl-2′-R-1′,2′- dihydro-2,3′-biquinolines. 2006 Springer Science+Business Media, Inc.

Investigations on 2,3′-biquinolyls. 12. Alkylation and arylation of 2,3′-biquinolyl dianion with organometallic compounds. New type of reaction for dianions of aromatic compounds

Aksenov,Aksenova,Smushkevich

, p. 976 - 981 (2007/10/03)

2,3′-Biquinolyl dianion reacts with organolithium and organomagnesium compounds with the formation, after treatment of the reaction mixture with water, of 2′-alkyl(aryl)-1′,2′-dihydro-2,3′-biquinolyls, and, after treatment of the reaction mixture with alkyl halides, of 1′-alkyl-2′-alkyl(aryl)- 1′,2′-dihydro-2,3′-biquinolyls. The reaction includes attack of the nucleophilic reagent with an electron transfer to a molecule of solvent.

Investigation of 2,3′-biquinolyl. 10. The regioselectivity of the reaction of 2,3′-biquinolyl and 1′-alkyl-3-(2-quinolyl)quinolinium halides with halo derivatives in the presence of metallic lithium and magnesium

Aksenov,Nadein

, p. 1314 - 1318 (2007/10/03)

2,3′-Biquinolyl reacts with halo derivatives in the presence of metallic lithium to give addition products at position 4′, treatment of which with water gives 4′-R-1′,4′-dihydro-2,3′-biquinolyls and with halo derivatives gives 1′-alkyl-4′-R-1′,4′-dihydro-2,3′-biquinolyls. The reaction of 2,3′-biquinolyl with halo derivatives in the presence of metallic magnesium gives a mixture of products of addition at positions 2′ and 4′. 1-Alkyl-3-(2-quinolyl)quinolinium halides and halo derivatives with metallic magnesium give 1′-alkyl-2′-R-1′,2′-dihydro-2,3′-biquinolyls but form a complex mixture of substances when metallic lithium is used.

Investigations of 2,3′-biquinolyl. 9. Reaction of 1′,4′-dihydro-2,3′-biquinolyl with organolithium compounds

Aksenov,Sarapy,Smushkevich

, p. 952 - 955 (2007/10/03)

The 1′,4′-dihydro-2,3′-biquinolyl reacts with organolithium compounds to form the mixture of 4′-R-1′,4′-dihydro-2,3′-biquinolyls and 2′-R-1′,2′-dihydro-2,3′-biquinolyls in the ratio analogous to the conversion in the series of 2,3′-biquinolyl. The utiliza

Studies of 2,3′-biquinolyl. 6. Regioselectivity of nucleophilic addition of organometallic compounds to 1-aklyl-3-(2-quinolyl)quinolinium halides

Aksenov,Nadein,Moiseev,Smushkevich

, p. 804 - 808 (2007/10/03)

Nucleophilic addition of organometallic lithium and magnesium compounds to 1-alkyl-3-(2-quinolyl)quinolinium cations produces a mixture of the corresponding 1′-alkyl-2′-R-1′,2′-dihydro-2,3′-biquinolyls and 1′-alkyl-4′-R-1′,4′-dihydro-2,3′-biquinolyls. The

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