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(2E)-3-phenyl-2-propenyl [(4-methylphenyl)sulfonyl] carbamic acid ester is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

855422-02-5

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855422-02-5 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 855422-02-5 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 8,5,5,4,2 and 2 respectively; the second part has 2 digits, 0 and 2 respectively.
Calculate Digit Verification of CAS Registry Number 855422-02:
(8*8)+(7*5)+(6*5)+(5*4)+(4*2)+(3*2)+(2*0)+(1*2)=165
165 % 10 = 5
So 855422-02-5 is a valid CAS Registry Number.

855422-02-5Relevant academic research and scientific papers

Microwave-Assisted 1,3-Dioxa-[3,3]-Sigmatropic Rearrangement of Substituted Allylic Carbamates: Application to the Synthesis of Novel 1,3-Oxazine-2,4-dione Derivatives

Bou Zeid, Samar,Eid, Samar,Najjar, Fadia,Macé, Aurélie,Rivilla, Ivan,Cossío, Fernando P.,Dorcet, Vincent,Roisnel, Thierry,Carreaux, Fran?ois

, (2021/11/22)

In a first instance, the effect of the microwave irradiation on the 1,3-Dioxa-[3,3]-sigmatropic rearrangement of aryl allylic carbamates was investigated. Under these new conditions, the reaction acceleration was clearly highlighted compared to convention

Regio- And diastereoselective Pd-catalyzed aminochlorocyclization of allylic carbamates: scope, derivatization, and mechanism

Ariga, Elaine Miho,Carita Correra, Thiago,Matsushima, Jullyane Emi,McIndoe, J. Scott,Moreira Ribeiro, Francisco Wanderson,Omari, Isaac,Papa Spadafora, Bruna,Rodrigues, Alessandro,Soares, Priscila Machado Arruda,Vinhato, Elisangela,de Oliveira-Silva, Diogo

supporting information, p. 5595 - 5606 (2021/07/02)

The regio- and diastereoselective synthesis of oxazolidinonesviaa Pd-catalyzed vicinal C-N/C-Cl bond-forming reaction from internal alkenes of allylic carbamates is reported. The oxazolidinones are obtained in yields of 44 to 95% with high to excellent diastereoselectivities (from 6?:?1 to >20?:?1 dr) from readily available precursors. This process is scalable, and the products are suitable for the synthesis of useful amino alcohols. A detailed theoretical and experimental mechanistic study was carried out to describe that the reaction proceeds through ananti-aminopalladation of the alkene followed by an oxidative C-Pd(ii) cleavage with retention of the carbon stereochemistry to yield the major diastereomer. The role of Cu(ii) in a C-Cl bond-forming mechanism step has also been proposed.

1,3-Dioxa-[3,3]-sigmatropic Oxo-Rearrangement of Substituted Allylic Carbamates: Scope and Mechanistic Studies

Agirre, Maddalen,Henrion, Sylvain,Rivilla, Ivan,Miranda, José I.,Cossío, Fernando P.,Carboni, Bertrand,Villalgordo, José M.,Carreaux, Fran?ois

, p. 14861 - 14881 (2019/01/04)

An unexpected 1,3-dioxa-[3,3]-sigmatropic rearrangement during the treatment of aryl- and alkenyl-substituted allylic alcohols with activated isocyanates is reported. The reorganization of bonds is highly dependent on the electron density of the aromatic

Palladium catalyzed arylation of N-alkyl O-allyl carbamates: Synthesis of cinnamyl alcohols via Heck arylation

Ono, Keiji,Fugami, Keigo,Tanaka, Shuji,Tamaru, Yoshinao

, p. 4133 - 4136 (2007/10/02)

N-alkyl O-cinnamyl carbamates (3) were prepared in good yields by palladium catalyzed arylation of N-alkyl O-allyl carbamates (2) with aryl iodides.

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