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tert-butyldimethylsilyl cyclohexylideneazinate is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

75157-19-6

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75157-19-6 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 75157-19-6 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 7,5,1,5 and 7 respectively; the second part has 2 digits, 1 and 9 respectively.
Calculate Digit Verification of CAS Registry Number 75157-19:
(7*7)+(6*5)+(5*1)+(4*5)+(3*7)+(2*1)+(1*9)=136
136 % 10 = 6
So 75157-19-6 is a valid CAS Registry Number.

75157-19-6Downstream Products

75157-19-6Relevant academic research and scientific papers

New and improved methods for the conversion of nitroalkanes into geminal chloronitroso compounds

Bou-Moreno, Rafael,Luengo-Arratta, Sandra,Pons, Valerie,Motherwell, William B.

, p. 6 - 12 (2013)

The scope and limitations of a new method for the preparation of geminal chloronitroso compounds involving treatment of a nitronate anion with oxalyl chloride are described in full, and a milder, high yielding, and more chemoselective variant using the de

Six-Membered Cyclic Nitroso Acetals: Synthesis and Studies of the Nitrogen Inversion Process of N-Silyloxy-3,6-dihydro-2H-1,2-oxazines

Shved, Alexander S.,Tabolin, Andrey A.,Novikov, Roman A.,Nelyubina, Yulia V.,Timofeev, Vladimir P.,Ioffe, Sema L.

supporting information, p. 5569 - 5578 (2016/11/25)

Silyl nitronates undergo rhodium-catalyzed formal [3+3]-cycloaddition with enol diazoacetates to form N-silyloxy-3,6-dihydro-2H-1,2-oxazines. The scope of the reaction and the extent of the major side process were evaluated. A mechanistic scheme was propo

THE NEF REACTION ON TRIALKYLSILYL NITRONATES PROMOTED BY m-CHLOROPERBENZOIC ACID, AN EFFICIENT ROUTE TO α-ALKOXYKETONES FROM NITROALKANES

Aizpurus, J. M.,Oiarbide, M.,Palomo, C.

, p. 5361 - 5364 (2007/10/02)

Treatment of a nitroalkene with nucleophiles, followed by silylation of the resulting nitroalkane and subsequent treatment with m-chloroperbenzoic acid provides α-functionalized carbonyl compounds in good yields.

SYNTHESIS, PROPERTIES, AND CRYSTAL STRUCTURE OF SILYL NITRONATES (SILYL ESTERS OF ACI-NITROALKANES): TOWARDS THE SN2 REACTION PATH WITH RETENTION OF CONFIGURATION AT SILICON

Colvin, Ernest W.,Beck, Albert K.,Bastani, Bahram,Seebach, Dieter,Kai, Yasushi,Dunitz, Jack D.

, p. 697 - 710 (2007/10/02)

An efficient and flexible method for the preparation of silyl nitronates is described (see 1-10).NMR. spectral investigations indicate a rapid 1,3-silyl migration process, with an activation energy of about 10 kcal mol-1.X-ray crystallographic

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