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The chemical compound "(C4H9)3SnCH(C6H5)CH(C6H5)CN" is a complex organotin compound with a molecular formula of C26H31NSn. It consists of a central tin (Sn) atom bonded to three butyl (C4H9) groups and a cyano (CN) group. The structure also includes two phenyl (C6H5) groups attached to a central carbon atom, which is bonded to the tin atom. (C4H9)3SnCH(C6H5)CH(C6H5)CN is characterized by its organometallic nature, with the tin atom acting as a central node connecting the organic groups. It is likely to have unique chemical properties due to the presence of the tin atom and the cyano group, which can participate in various chemical reactions, such as nucleophilic substitutions or addition reactions. The compound's structure suggests potential applications in areas such as polymer chemistry, where organotin compounds are used as catalysts or stabilizers, or in the synthesis of more complex organometallic compounds.

78887-92-0

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78887-92-0 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 78887-92-0 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 7,8,8,8 and 7 respectively; the second part has 2 digits, 9 and 2 respectively.
Calculate Digit Verification of CAS Registry Number 78887-92:
(7*7)+(6*8)+(5*8)+(4*8)+(3*7)+(2*9)+(1*2)=210
210 % 10 = 0
So 78887-92-0 is a valid CAS Registry Number.

78887-92-0Downstream Products

78887-92-0Relevant academic research and scientific papers

ORGANOTIN HYDRIDE ADDITIONS TO E- AND Z-TRISUBSTITUTED ETHYLENES.SYNTHESIS OF SOME NEW FUNCTIONALLY SUBSTITUTED ORGANOTIN COMPOUNDS

Podesta, J. C.,Chopa, A. B.,Ayala, A.D.

, p. 163 - 170 (2007/10/02)

The syntheses of some new functionally substituted organotin compounds are reported.The results indicate that the additions of tri-n-butyltin and tri-phenyltin hydrides to trisubstituted ethylenes (where one substituent is either a carbomethoxy or a nitrile group) proceed smoothly to give high yields of organotin adducts and that the reactions are stereoselective.Evidence concerning the reversibility of the free radical forming step is presented.

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