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Benzenemethanol, α-phenyl-α-(triphenylgermyl)-, also known as α-phenyl-α-(triphenylgermyl)benzenemethanol, is an organic compound with the molecular formula C26H22GeO. It is a derivative of benzenemethanol, featuring a phenyl group and a triphenylgermyl group attached to the carbon atom adjacent to the hydroxyl group. Benzenemethanol, a-phenyl-a-(triphenylgermyl)- is characterized by its unique structure, which combines the aromatic properties of benzene with the heavier group 14 element, germanium. It is of interest in organic chemistry, particularly in the study of organogermanium compounds, and may have potential applications in the synthesis of complex organic molecules and materials.

4639-78-5

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4639-78-5 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 4639-78-5 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 4,6,3 and 9 respectively; the second part has 2 digits, 7 and 8 respectively.
Calculate Digit Verification of CAS Registry Number 4639-78:
(6*4)+(5*6)+(4*3)+(3*9)+(2*7)+(1*8)=115
115 % 10 = 5
So 4639-78-5 is a valid CAS Registry Number.

4639-78-5Downstream Products

4639-78-5Relevant academic research and scientific papers

ASSISTANCE NUCLEOPHILE DANS DES REACTIONS DE REDUCTION D'ORGANOHALOGENO- ET HALOGENO-GERMANES PAR DES REDUCTEURS DOUX R3M(IVB)-H ET RCHO: GERMYLANIONS, DERIVES FONCTIONNELS DU GERMANIUM

Castel, A.,Riviere, P.,Satge, J.

, p. 137 - 146 (2007/10/02)

Catalytic activity of nuclophiles such as tertiary amines and diazo derivatives in the reduction of halogermanes by means of gentle reductive agents, such as R3M(IVB)-H or RCHO, has been shown.In the particular case of enolisable aldehyde, a competition between nucleophilic substitution at the metal and germanium-halogen bond reduction has been observed.Transposition of enoxygermanes formed through the substitution process, leads to β-germylaldehydes.

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