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methyl 2-hydroxy-2-(2-iodophenyl)acetate is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

90347-69-6

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90347-69-6 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 90347-69-6 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 9,0,3,4 and 7 respectively; the second part has 2 digits, 6 and 9 respectively.
Calculate Digit Verification of CAS Registry Number 90347-69:
(7*9)+(6*0)+(5*3)+(4*4)+(3*7)+(2*6)+(1*9)=136
136 % 10 = 6
So 90347-69-6 is a valid CAS Registry Number.

90347-69-6Downstream Products

90347-69-6Relevant academic research and scientific papers

Boron-catalyzed CC functionalization of allyl alcohols

Rao, Santhosh,Kapanaiah, Raja,Prabhu, Kandikere Ramaiah

supporting information, p. 1301 - 1306 (2019/10/28)

Tris(pentafluorophenyl)borane-catalyzed CC bond functionalization of arylallyl alcohols using donor-acceptor carbenes is presented. The allylic hydroxyl group is found to assist the product formation by neighboring group participation providing a clue towards mechanistic understanding. This method can also be employed to effect homologation of allyl alcohols to homoallyl alcohols. Overall, this metal-free transformation presents a novel disconnection strategy towards carbon-carbon bond scission and formation.

Boron-Catalyzed C?C Functionalization of Allyl Alcohols

Rao, Santhosh,Kapanaiah, Raja,Prabhu, Kandikere Ramaiah

supporting information, (2019/02/14)

Tris(pentafluorophenyl)borane-catalyzed C?C bond functionalization of arylallyl alcohols using donor-acceptor carbenes is presented. The allylic hydroxyl group is found to assist the product formation by neighboring group participation providing a clue towards mechanistic understanding. This method can also be employed to effect homologation of allyl alcohols to homoallyl alcohols. Overall, this metal-free transformation presents a novel disconnection strategy towards carbon-carbon bond scission and formation. (Figure presented.).

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