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exo-2,4,6-triphenyl-1,3-diazabicyclo<3.1.0>hex-3-ene is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

28028-89-9

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28028-89-9 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 28028-89-9 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 2,8,0,2 and 8 respectively; the second part has 2 digits, 8 and 9 respectively.
Calculate Digit Verification of CAS Registry Number 28028-89:
(7*2)+(6*8)+(5*0)+(4*2)+(3*8)+(2*8)+(1*9)=119
119 % 10 = 9
So 28028-89-9 is a valid CAS Registry Number.

28028-89-9Downstream Products

28028-89-9Relevant academic research and scientific papers

Structure investigation of bridgehead aziridine: Synthesis, theoretical, and crystallographic study of 2,4,6-triphenyl-1,3-diazabicyclo[3.1.0]hex-3-ene

Bruno, Giuseppe,Nicolo, Francesco,Rotondo, Archimede,Risitano, Francesco,Grassi, Giovanni,Foti, Francesco

, p. 190 - 200 (2006)

A one-pot three-component procedure to efficiently create the 1,3-diazabicyclo[3.1.0]hex-3-ene system is reported. The molecular structure of 2,4,6-triphenyl-1,3-diazabicyclo[3.1.0]hex-3-ene (3) was studied by X-ray diffraction and compared to ab initio a

A novel efficient three-component one-pot synthesis of 1,3-diazabicyclo[3. 1.0]hex-3-ene system under microwave irradiation

Risitano, Francesco,Grassi, Giovanni,Foti, Francesco,Moraci, Sonia

, p. 1633 - 1635 (2007/10/03)

Bridgehead aziridines 3 were synthesized in high yields and excellent diastereocontrol by a three-component reaction of an aldehyde, phenacyl chloride and ammonium acetate in acetic acid using microwave irradiation. Georg Thieme Verlag Stuttgart.

AZIRIDINYL KETONES AND THEIR CYCLIC ANILS. 10. 2,4,6-TRIARYL-1,3-DIAZABICYCLOHEX-3-ENES

Orlov, V. D.,Kaluski, Z.,Figas, E.,Vorob'eva, N. P.,Bakumenko, A. I.,Yaremenko, F. G.

, p. 849 - 854 (2007/10/02)

2,4,6-Triaryl-1,3-diazabicyclohex-3-enes were prepared by the reaction of α,β-dibromochalcones with aromatic aldehydes and ammonia.The exo- and endo-isomers were isolated and characterized.X-ray structural analysis of the endo-6-(4-nitrophenyl)-2,4

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