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tert-butyl (2-(chloromethyl)-5-fluorophenyl)carbamate is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

1620102-85-3

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1620102-85-3 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 1620102-85-3 includes 10 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 7 digits, 1,6,2,0,1,0 and 2 respectively; the second part has 2 digits, 8 and 5 respectively.
Calculate Digit Verification of CAS Registry Number 1620102-85:
(9*1)+(8*6)+(7*2)+(6*0)+(5*1)+(4*0)+(3*2)+(2*8)+(1*5)=103
103 % 10 = 3
So 1620102-85-3 is a valid CAS Registry Number.

1620102-85-3Relevant academic research and scientific papers

N-Heterocyclic Carbene-Catalyzed Synthesis of 2-Aryl Indoles

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Paragraph 0038-0041; 0044-0045, (2015/11/27)

Transition metal-free catalytic methods for access to 2-arylindole compounds.

N-heterocyclic-carbene-catalyzed synthesis of 2-aryl indoles

Hovey, M. Todd,Check, Christopher T.,Sipher, Alexandra F.,Scheidt, Karl A.

, p. 9603 - 9607 (2014/10/15)

A convergent and efficient transition-metal-free catalytic synthesis of 2-aryl-indoles has been developed. The interception of a highly reactive and transient aza-ortho-quinone methide by an acyl anion equivalent generated through N-hetereocyclic carbene catalysis is central to this successful strategy. High yields and a wide scope as well as the streamlined synthesis of a kinase inhibitor are reported. Umpolung: N-heterocyclic carbene catalysis is used for the convergent and efficient transition-metal-free synthesis of 2-aryl-indoles. The interception of a highly reactive and transient aza-ortho-quinone methide by an acyl anion equivalent is central to this successful strategy. The reaction exhibits high yields and a wide scope, and it has been applied to a streamlined synthesis of a kinase inhibitor.

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