939759-26-9 Usage
General Description
3-IODO-AZETIDINE-1-CARBOXYLIC ACID BENZYL ESTER is a chemical compound that belongs to the class of organohalogen compounds. It is an ester derivative of azetidine-1-carboxylic acid, with a benzyl group attached to the carboxylic acid functional group. 3-IODO-AZETIDINE-1-CARBOXYLIC ACID BENZYL ESTER is used in organic synthesis and pharmaceutical research, particularly in the development of potential drug candidates. It has potential applications in the field of medicinal chemistry and drug discovery due to its unique structural and chemical properties. However, it is important to handle this compound with caution and follow proper safety protocols due to its potentially hazardous nature.
Check Digit Verification of cas no
The CAS Registry Mumber 939759-26-9 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 9,3,9,7,5 and 9 respectively; the second part has 2 digits, 2 and 6 respectively.
Calculate Digit Verification of CAS Registry Number 939759-26:
(8*9)+(7*3)+(6*9)+(5*7)+(4*5)+(3*9)+(2*2)+(1*6)=239
239 % 10 = 9
So 939759-26-9 is a valid CAS Registry Number.
InChI:InChI=1/C11H12INO2/c12-10-6-13(7-10)11(14)15-8-9-4-2-1-3-5-9/h1-5,10H,6-8H2
939759-26-9Relevant articles and documents
Mild and phosphine-free iron-catalyzed cross-coupling of nonactivated secondary alkyl halides with alkynyl grignard reagents
Cheung, Chi Wai,Ren, Peng,Hu, Xile
supporting information, p. 2566 - 2569 (2014/05/20)
A simple protocol for iron-catalyzed cross-coupling of nonactivated secondary alkyl bromides and iodides with alkynyl Grignard reagents at room temperature has been developed. A wide range of secondary alkyl halides and terminal alkynes are tolerated to a
Chiral proton catalysis of secondary nitroalkane additions to azomethine: Synthesis of a potent GlyT1 inhibitor
Davis, Tyler A.,Danneman, Michael W.,Johnston, Jeffrey N.
supporting information; experimental part, p. 5578 - 5580 (2012/07/17)
The first enantioselective synthesis of a potent GlyT1 inhibitor is described. A 3-nitroazetidine donor is used in an enantioselective aza-Henry reaction catalyzed by a bis(amidine)-triflic acid salt organocatalyst, delivering the key intermediate with 92% ee. This adduct is reductively denitrated and converted to the target through a short sequence, thereby allowing assignment of the absolute configuration of the more potent enantiomer.
