1435-04-7 Usage
General Description
Phenol, 2-[(2-thienylmethylene)amino]- is a chemical compound that consists of a phenol ring attached to a 2-[(2-thienylmethylene)amino] group. The compound is a derivative of phenol, with the amino group attached to a thienylmethylene group. It is commonly used in organic synthesis and can react with various reagents to form new compounds. The presence of the thienylmethylene group adds unique properties and reactivity to the molecule, making it important in the development of pharmaceuticals and other organic compounds. Its structure allows for a wide range of potential reactions and applications in chemical research and industry.
Check Digit Verification of cas no
The CAS Registry Mumber 1435-04-7 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 1,4,3 and 5 respectively; the second part has 2 digits, 0 and 4 respectively.
Calculate Digit Verification of CAS Registry Number 1435-04:
(6*1)+(5*4)+(4*3)+(3*5)+(2*0)+(1*4)=57
57 % 10 = 7
So 1435-04-7 is a valid CAS Registry Number.
InChI:InChI=1/C11H9NOS/c13-11-6-2-1-5-10(11)12-8-9-4-3-7-14-9/h1-8,13H/b12-8+
1435-04-7Relevant articles and documents
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Eichhorn,Bailar
, p. 2905 (1953)
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Base-Free and Catalyst-Free Synthesis of Functionalized Dihydrobenzoxazoles via Vinylogous Carbonate to Carbamate Rearrangement
Das, Tamal Kanti,Mondal, Santigopal,Gonnade, Rajesh G.,Biju, Akkattu T.
supporting information, p. 5597 - 5600 (2017/10/25)
An unexpected, catalyst-free, and base-free intramolecular cyclization of N-aryloxyacrylate aldimines, under thermal conditions leading to the synthesis of functionalized dihydrobenzoxazoles, is reported. The reaction features a unique rearrangement of vi
Highly enantioselective imine cinnamylation with a remarkable diastereochemical switch
Huber, John D.,Leighton, James L.
, p. 14552 - 14553 (2008/09/19)
The first general method for the enantioselective cinnamylation of aldimines is reported. The method utilizes a simple chiral cinnamylsilane reagent and is characterized by experimental simplicity and extraordinarily high levels of enantioselectivity. Fur
