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((1S,2S,3S,4R)-3-(2-nitrophenyl)bicyclo[2.2.1]hept-5-en-2-yl)methanol is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

1476807-36-9

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1476807-36-9 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 1476807-36-9 includes 10 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 7 digits, 1,4,7,6,8,0 and 7 respectively; the second part has 2 digits, 3 and 6 respectively.
Calculate Digit Verification of CAS Registry Number 1476807-36:
(9*1)+(8*4)+(7*7)+(6*6)+(5*8)+(4*0)+(3*7)+(2*3)+(1*6)=199
199 % 10 = 9
So 1476807-36-9 is a valid CAS Registry Number.

1476807-36-9Downstream Products

1476807-36-9Relevant academic research and scientific papers

Chiral GAP catalysts of phosphonylated imidazolidinones and their applications in asymmetric Diels-Alder and Friedel-Crafts reactions

Qiao, Shuo,Mo, Junming,Wilcox, Cody B.,Jiang, Bo,Li, Guigen

, p. 1718 - 1724 (2017)

The design and synthesis of recyclable imidazolidinone catalysts using GAP chemistry/technique was described. Their applications in asymmetric Diels-Alder and Friedel-Crafts reactions with α,β-unsaturated aldehydes resulted in excellent yields and higher enantioselectivities than previous processes. As recyclable small molecular catalysts, phosphonylated imidazolidinones can be recovered and reused for up to three runs without costing significant decrease in catalytic activity.

Non-Covalently Immobilized Chiral Imidazolidinone on Sulfated-Chitin: Reusable Heterogeneous Organocatalysts for Asymmetric Diels-Alder Reaction

Watanabe, Mirai,Sakai, Takuya,Oka, Marina,Makinose, Yuki,Miyazaki, Hidetoshi,Iida, Hiroki

supporting information, p. 255 - 260 (2019/12/11)

A heterogeneous chiral imidazolodinone catalyst was synthesized by immobilization on a sulfated chitin through non-covalent ionic interactions. The chitin-based organocatalyst promoted the asymmetric Diels-Alder reaction with high enantioselectivity under heterogeneous conditions and was successfully reused multiple times without apparent loss of catalytic activity and enantioselectivity.

Novel binaphthyl and biphenyl α- and β-amino acids and esters: organocatalysis of asymmetric Diels-Alder reactions. A combined synthetic and computational study

Bulman Page, Philip C.,Kinsey, Francesca S.,Chan, Yohan,Strutt, Ian R.,Slawin, Alexandra M. Z.,Jones, Garth A.

supporting information, p. 7400 - 7416 (2018/10/24)

Asymmetric catalysis of the Diels-Alder reaction between cyclopentadiene and cinnamaldehydes has been studied using as catalysts a range of novel α- and β-aminoacids and aminoesters with binaphthyl and biphenyl backbones, providing enantioselectivities of

Chiral hybrid inorganic-organic materials: Synthesis, characterization, and application in stereoselective organocatalytic cycloadditions

Puglisi, Alessandra,Benaglia, Maurizio,Annunziata, Rita,Chiroli, Valerio,Porta, Riccardo,Gervasini, Antonella

, p. 11326 - 11334 (2013/12/04)

The synthesis of chiral imidazolidinones on mesoporous silica nanoparticles, exploiting two different anchoring sites and two different linkers, is reported. Catalysts 1-4 were prepared starting from l-phenylalanine or l-tyrosine methyl esters and support

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