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1010396-60-7

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1010396-60-7 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 1010396-60-7 includes 10 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 7 digits, 1,0,1,0,3,9 and 6 respectively; the second part has 2 digits, 6 and 0 respectively.
Calculate Digit Verification of CAS Registry Number 1010396-60:
(9*1)+(8*0)+(7*1)+(6*0)+(5*3)+(4*9)+(3*6)+(2*6)+(1*0)=97
97 % 10 = 7
So 1010396-60-7 is a valid CAS Registry Number.

1010396-60-7Relevant articles and documents

Formal [3+2] annulation involving allylic bromides and thioureas. synthesis of 2-iminothiazolidines through a base-catalyzed intramolecular anti-Michael addition

Ferreira, Misael,Sá, Marcus M.

, p. 829 - 833 (2015)

A simple and efficient protocol was developed for the synthesis of 2-iminothiazolidines through a base-mediated [3+2] annulation involving substituted thioureas and allylic bromides bearing electron-withdrawing groups. This domino process consists of nucleophilic displacement, followed by intramolecular anti-Michael addition of the preformed allylic isothiourea under mild conditions to give the thiazolidine core.

Design, synthesis and evaluation of 3-arylidene azetidin-2-ones as potential antifungal agents against Alternaria solani Sorauer

Delong, Wang,Yongling, Wu,Lanying, Wang,Juntao, Feng,Xing, Zhang

, p. 6661 - 6673 (2017/11/17)

A new concise and facile method was explored to synthesize a collection of new 3-arylidene azetidin-2-ones, which could be regarded as the derivatives of the hybrid scaffold of bioactive natural cinnamamide and heterocycle azetidi-2-one. The structures of

A phenacrylate scaffold for tunable thiol activation and release

Sankar, Rathinam K.,Kumbhare, Rohan S.,Dharmaraja, Allimuthu T.,Chakrapani, Harinath

supporting information, p. 15323 - 15326 (2015/01/09)

A thiol-selective 2-methyl-3-phenacrylate scaffold with spatiotemporal control over delivery of a cargo is reported. The half-lives of decomposition could be tuned from 30 min to 1 day and the scaffold's utility in thiol-inducible fluorophore release in cell-free as well as within cells is demonstrated.

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