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β-(N,N-dimethylamino)-β-trimethylsiloxystyrene is a complex organic compound that combines the properties of an amine, a styrene derivative, and a silane. It features a β-dimethylamino group, which is an electron-donating group that can influence the reactivity and stability of the molecule. The trimethylsilyl group is a common protecting group in organic synthesis, known for its ability to stabilize certain functional groups and its ease of removal under mild conditions. The styrene moiety, with its vinyl group, is a key component in the production of polystyrene and other polymers. β-(N,N-dimethylamino)-β-trimethylsiloxystyrene is likely to be used in advanced materials science, potentially in the synthesis of specialty polymers or as an intermediate in the preparation of other complex organic molecules. Its unique structure suggests that it could have applications in areas such as electronics, where materials with specific electronic properties are required, or in the pharmaceutical industry for the development of new drugs.

75580-92-6

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75580-92-6 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 75580-92-6 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 7,5,5,8 and 0 respectively; the second part has 2 digits, 9 and 2 respectively.
Calculate Digit Verification of CAS Registry Number 75580-92:
(7*7)+(6*5)+(5*5)+(4*8)+(3*0)+(2*9)+(1*2)=156
156 % 10 = 6
So 75580-92-6 is a valid CAS Registry Number.

75580-92-6Relevant academic research and scientific papers

STRUCTURE DU REACTIF D'IVANOV ET DE QUELQUES ORGANOMETALLIQUES ISSUS DES DERIVES PHENYLACETIQUES-I. ETUDE DES SOLUTIONS PAR RMN

Mladenova, M.,Blagoev, B.,Gaudemar, M.,Dardoize, F.,Lallemand, J. Y.

, p. 2153 - 2156 (2007/10/02)

Ivanov reagent and several analogous reagents (phenyl acetique serie) have been studied by NMR.In all the cases, an enolate-structure is revealed; no carbaneniate-species could be detected, even in very solvating solvents.

Synthesis of α-fluorocarbonyl compounds

-

, (2008/06/13)

Process for preparing an organic compound of the formula R2 R2 CFC(O)R3, which process comprises contacting and reacting in a reaction mixture which includes an inert solvent, at a temperature of -40° C. to -100° C., ROF and STR1 R is polyfluoroperhaloalkyl of 1-6 carbon atoms or FOCF2 ; R1 is hydrocarbyl of 1-6 carbon atoms; each R2 is selected from H, alkyl of 1-17 carbon atoms, cycloalkyl of 3-6 carbon atoms, aryl, heteroaryl and such alkyl, cycloalkyl, aryl and heteroaryl substituted by halogen or alkoxy of 1-6 carbon atoms; R3 is selected from H, alkyl and haloalkyl of 1-16 carbon atoms, cycloalkyl of 3-10 carbon atoms, aryl and haloaryl, OSi(R1)3, OH, NH2, alkoxy of 1-6 carbon atoms, aryloxy, NHR1 and NR12 wherein R1 is alkyl of 1-6 carbon atoms, N-arylamino and nitrogen or sulfur heterocyclic of 4-5 carbon atoms; R3 and one R2 taken together is a diradical which with the C=C group is carbocyclic, heterocyclic or haloheterocyclic, and recovering from the reaction mixture the compound of the formula R2 R2 CFC(O)R3.

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