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1040308-67-5

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1040308-67-5 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 1040308-67-5 includes 10 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 7 digits, 1,0,4,0,3,0 and 8 respectively; the second part has 2 digits, 6 and 7 respectively.
Calculate Digit Verification of CAS Registry Number 1040308-67:
(9*1)+(8*0)+(7*4)+(6*0)+(5*3)+(4*0)+(3*8)+(2*6)+(1*7)=95
95 % 10 = 5
So 1040308-67-5 is a valid CAS Registry Number.

1040308-67-5Relevant academic research and scientific papers

Bis(dibenzylideneacetone)palladium(0)/tert-Butyl Nitrite- Catalyzed Cyclization of o-Alkynylanilines with tert-Butyl Nitrite: Synthesis and Applications of Indazole 2-Oxides

Senadi, Gopal Chandru,Wang, Ji-Qi,Gore, Babasaheb Sopan,Wang, Jeh-Jeng

, p. 2747 - 2753 (2017/08/23)

An efficient method for the synthesis of 1-benzyl/arylindazole 2-oxides via a bis(dibenzylideneacetone)palladium(0) [Pd(dba)2]/tert-butyl nitrite (TBN)-catalyzed reaction of o-alkynylaniline derivatives with TBN is reported. The overall transfo

Pd-catalyzed ring assembly by vinylation and intramolecular heck coupling: A versatile strategy towards functionalized azadibenzocyclooctynes

J?ger, Michael,G?rls, Helmar,Günther, Wolfgang,Schubert, Ulrich S.

supporting information, p. 2150 - 2157 (2013/03/28)

A new modular approach based on Pd-catalyzed C-C bond formation is presented for the assembly of a benzannulated azocine scaffold, the key intermediate in the synthesis of functionalized azadibenzocyclooctynes (aza-DIBOs). The intramolecular ring-closing Heck coupling was investigated by variation of the C-X bond. The reaction rate is limited by the initial oxidative addition step and the regiochemistry strongly depends on the auxiliary phosphine. Under optimized conditions, the 8-endo regioisomer was obtained in 71 % yield over two steps (with no protecting group chemistry) or in one pot, inclusive of C-N bond formation. The practical generation of the octyne triple bond of a prototypical N-benzoyl aza-DIBO, without the need for chromatographic purification, is also described. The structural features, including those of the ring-strained cyclic octyne, were elucidated by NMR spectroscopy and X-ray crystallographic analysis. The high reactivity of the N-benzoyl aza-DIBO synthesized is demonstrated in a strain-promoted azide-alkyne cycloaddition reaction with an alkyl azide (k=0.38 M-1 s-1). Copyright

A facile copper-catalyzed one-pot domino synthesis of 5,12-dihydroindolo[2, 1- b ]quinazolines

Jiang, Min,Li, Jian,Wang, Feng,Zhao, Yichao,Zhao, Feng,Dong, Xiaochun,Zhao, Weili

, p. 1420 - 1423 (2012/05/05)

A domino synthesis of 5,12-dihydroindolo[2,1-b]quinazoline derivatives via copper-catalyzed Ullmann-type intermolecular C-C and intramolecular C-N couplings is reported. Good yields of various 5,12-dihydroindolo[2,1-b] quinazoline derivatives were obtained. Reaction scopes, limitations, and the reaction mechanism are discussed.

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