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2-benzoic acid methyl ester is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

1025359-66-3

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1025359-66-3 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 1025359-66-3 includes 10 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 7 digits, 1,0,2,5,3,5 and 9 respectively; the second part has 2 digits, 6 and 6 respectively.
Calculate Digit Verification of CAS Registry Number 1025359-66:
(9*1)+(8*0)+(7*2)+(6*5)+(5*3)+(4*5)+(3*9)+(2*6)+(1*6)=133
133 % 10 = 3
So 1025359-66-3 is a valid CAS Registry Number.

1025359-66-3Downstream Products

1025359-66-3Relevant academic research and scientific papers

Halogen-Bond-Induced Consecutive Csp3-H Aminations via Hydrogen Atom Transfer Relay Strategy

Alom, Nur-E,Ariyarathna, Jeewani P.,Bassiouni, Omar H.,Kaur, Navdeep,Kennell, Maureen L.,Li, Wei,Wu, Fan

, p. 2135 - 2140 (2020/04/09)

The utilization of a halogen bond in a number of chemical fields is well-known. Surprisingly, the incorporation of this useful noncovalent interaction in chemical reaction engineering is rare. We disclose here an uncommon use of halogen bonding to induce intermolecular Csp3-H amination while enabling a hydrogen atom transfer relay strategy to access privileged pyrrolidine structures directly from alkanes. Mechanistic studies support the presence of multiple halogen bond interactions at distinct reaction stages.

Copper triflate/t-BuOOAc-catalyzed amidation of allylic and benzylic acetates with sulfonamides

Powell, David A.,Pelletier, Guillaume

, p. 2495 - 2498 (2008/09/19)

A copper triflate/t-BuOOAc-catalyzed amidation of allylic and benzylic acetates has been developed which is suitable for the coupling of a wide variety of functionalized sulfonamide nucleophiles with acetate electrophiles. The methodology allows for the amidation of benzylic substrates which are not further activated by an additional adjacent alkene or alkyne, enabling simple allylic acetates and primary benzylic acetates to be used as reaction partners.

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