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1270077-22-9

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1270077-22-9 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 1270077-22-9 includes 10 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 7 digits, 1,2,7,0,0,7 and 7 respectively; the second part has 2 digits, 2 and 2 respectively.
Calculate Digit Verification of CAS Registry Number 1270077-22:
(9*1)+(8*2)+(7*7)+(6*0)+(5*0)+(4*7)+(3*7)+(2*2)+(1*2)=129
129 % 10 = 9
So 1270077-22-9 is a valid CAS Registry Number.

1270077-22-9Downstream Products

1270077-22-9Relevant academic research and scientific papers

Ruthenium-Catalyzed Transfer Oxygenative [2 + 2 + 1] Cycloaddition of Silyldiynes Using Nitrones as Adjustable Oxygen Atom Donors. Synthesis of Bicyclic 2-Silylfurans

Matsui, Kazuma,Shibuya, Masatoshi,Yamamoto, Yoshihiko

, p. 6468 - 6472 (2015)

The first example of the Ru-catalyzed transfer oxygenative [2 + 2 + 1] cycloaddition of silyldiynes to produce bicyclic 2-silylfurans is described. This cyclization process was realized using nitrones as readily available and adjustable oxygen atom donors

A combined transition-metal-catalyzed and photopromoted process: Synthesis of 2,3-fused 4-phenylnaphthalen-1-yl carboxylates from 1,7-diaryl-1,6-diynes

Yamamoto, Yoshihiko,Mori, Shota,Shibuya, Masatoshi

supporting information, p. 9093 - 9100 (2015/06/16)

2,3-Fused 4-phenylnaphthalen-1-yl carboxylates were synthesized in a step- and atom-economical manner using a ruthenium-catalyzed hydrocarboxylative cyclization of 1,7-diaryl-1,6-diynes and subsequent oxidative photocyclization. The scope of this novel two-step process was demonstrated by the construction of diverse structures from substrates with various tethers and terminal aryl groups. Late-stage C-H functionalizations of the arylnaphthalene product further enhance the synthetic potential of the developed process. Light a fuse! 2,3-Fused 4-phenylnaphthalen-1-yl carboxylates were synthesized in a step- and atom-economical manner using a ruthenium-catalyzed hydrocarboxylative cyclization of 1,7-diaryl-1,6-diynes and subsequent oxidative photocyclization. Late-stage C-H functionalizations of the obtained arylnaphthol derivatives further enhance the synthetic potential of the developed process (see scheme).

Ruthenium-catalyzed transfer oxygenative cyclization of α,ω-diynes: Unprecedented [2 + 2 + 1] route to bicyclic furans via ruthenacyclopentatriene

Yamashita, Ken,Yamamoto, Yoshihiko,Nishiyama, Hisao

supporting information; experimental part, p. 7660 - 7663 (2012/06/30)

A novel oxygen-atom-transfer process enables the catalytic [2 + 2 + 1] synthesis of bicyclic furans from α,ω-diynes with DMSO. [CpRu(AN)3]PF6 catalyzed the transfer oxygenative cyclization of diynes with aryl terminal groups, while t

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