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1-(2-selenocyanatophenyl)ethan-1-one is an organic compound with the molecular formula C9H7NOSe. It is a derivative of acetophenone, where one of the hydrogen atoms on the phenyl ring is replaced by a selenocyanate group (-SeCN). 1-(2-selenocyanatophenyl)ethan-1-one is characterized by its selenophene ring, which contains selenium, and its nitrile group, which is a triple-bonded carbon-nitrogen functional group. It is a colorless to pale yellow solid and is used in the synthesis of various organic compounds, particularly those involving selenium. Due to its reactivity, it is typically handled with care in a laboratory setting.

1441-75-4

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1441-75-4 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 1441-75-4 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 1,4,4 and 1 respectively; the second part has 2 digits, 7 and 5 respectively.
Calculate Digit Verification of CAS Registry Number 1441-75:
(6*1)+(5*4)+(4*4)+(3*1)+(2*7)+(1*5)=64
64 % 10 = 4
So 1441-75-4 is a valid CAS Registry Number.

1441-75-4Relevant academic research and scientific papers

Metal-free visible light-promoted synthesis of isothiazoles: A catalytic approach for N-S bond formation from iminyl radicals under batch and flow conditions

Alemán, José,Berton, Mateo,Cabrera-Afonso, María Jesús,Cembellín, Sara,Halima-Salem, Adnane,Maestro, M. Carmen,Marzo, Leyre,Miloudi, Abdellah

supporting information, p. 6792 - 6797 (2020/11/09)

A sustainable synthesis of isothiazoles has been developed using an α-amino-oxy acid auxiliary and applying photoredox catalysis. This simple strategy features mild conditions, broad scope and wide functional group tolerance representing a new enviromenta

Oxidation of organoselenium compounds. A study of chemoselectivity of phenylacetone monooxygenase

Andrade, Leandro H.,Pedrozo, Eliane C.,Leite, Henrique G.,Brondani, Patricia B.

scheme or table, p. 63 - 66 (2012/02/13)

Organoselenium acetophenones oxidation using enzymatic reactions has been developed and chemoselectivity of phenylacetone monooxygenase (PAMO) with selenium-containing ketones has been explored. We discovered that this biocatalyst prefers selenium oxidation, which leads to selenoxide in excellent conversion, over Baeyer-Villiger oxidation.

ω-Transaminases as efficient biocatalysts to obtain novel chiral selenium-amine ligands for Pd-catalysis

Andrade, Leandro H.,Silva, Alexandre V.,Milani, Priscila,Koszelewski, Dominik,Kroutil, Wolfgang

experimental part, p. 2043 - 2051 (2010/07/03)

ω-Transaminases have been evaluated as biocatalysts in the reductive amination of organoselenium acetophenones to the corresponding amines, and in the kinetic resolution of racemic organoselenium amines. Kinetic resolution proved to be more efficient than the asymmetric reductive amination. By using these methodologies we were able to obtain both amine enantiomers in high enantiomeric excess (up to 99%). Derivatives of the obtained optically pure o-selenium 1-phenylethyl amine were evaluated as ligands in the palladium-catalyzed asymmetric alkylation, giving the alkylated product in up to 99% ee.

First dynamic kinetic resolution of selenium-containing chiral amines catalyzed by palladium (Pd/BaSO4) and Candida antartica lipase (CAL-B)

Andrade, Leandro H.,Silva, Alexandre V.,Pedrozo, Eliane C.

scheme or table, p. 4331 - 4334 (2009/10/26)

An efficient method for chemoenzymatic dynamic kinetic resolution of selenium-containing chiral amines (organoselenium-1-phenylethanamines) has been developed, leading to the corresponding amides in excellent enantioselectivities and high isolated yields.

First chemoenzymatic synthesis of organoselenium amines and amides

Andrade, Leandro H.,Silva, Alexandre V.

, p. 1175 - 1181 (2008/09/21)

A series of organoselenium amines have been synthesized and submitted to the enzymatic kinetic resolution by acetylation mediated by CAL-B (Novozym 435) to give the corresponding chiral amides in an enantiomerically pure form. After evaluating the appropriate lipase, solvent, temperature, and lipase/substrate ratio in the kinetic resolution, the chiral organoselenium amides were obtained with enantiomeric excess of up to 99%.

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