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α-tri-n-butylgermylstyrene is an organogermanium compound characterized by the presence of a germyl group (GeR3) attached to a styrene moiety. α-tri-n-butylgermylstyrene is composed of a styrene unit, which is a vinylbenzene molecule, and a tri-n-butylgermyl group, which consists of a germanium atom bonded to three n-butyl groups. The chemical structure can be represented as (CH3CH2CH2CH2)3Ge-C6H5-CH=CH2. α-tri-n-butylgermylstyrene is of interest in the field of organometallic chemistry due to its unique properties, such as its potential applications in polymer chemistry and as a precursor for the synthesis of more complex organogermanium compounds. The compound's stability, reactivity, and electronic properties make it a subject of study for understanding the behavior of heavier group 14 elements in organic chemistry.

38796-03-1

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38796-03-1 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 38796-03-1 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 3,8,7,9 and 6 respectively; the second part has 2 digits, 0 and 3 respectively.
Calculate Digit Verification of CAS Registry Number 38796-03:
(7*3)+(6*8)+(5*7)+(4*9)+(3*6)+(2*0)+(1*3)=161
161 % 10 = 1
So 38796-03-1 is a valid CAS Registry Number.

38796-03-1Downstream Products

38796-03-1Relevant academic research and scientific papers

Cobalt-Catalyzed (E)-β-Selective Hydrogermylation of Terminal Alkynes

Radzhabov, Maxim R.,Mankad, Neal P.

supporting information, p. 3221 - 3226 (2021/05/04)

A cobalt-catalyzed method for the hydrogermylation of alkynes is reported, providing a selective and accessible route to (E)-β-vinyl(trialkyl)germanes from terminal alkynes and HGeBu3. As shown in multiple examples, the developed method demonstrates a broad functional group tolerance an practical utility for late-stage hydrogermylation of natural products. The method is compatible with alkynes bearing both aryl and alkyl substituents, providing unrivaled selectivity for previously challenging 1° alkyl-substituted alkynes. Moreover, the catalyst used in this method, Co2(CO)8, is a cheap and commercially available reagent. Conducted mechanistic studies supported the syn-addition of Bu3GeH to an alkyne π-complex.

Transition metal-catalyzed dehydrogenative germylation of olefins with tri-n-butylgermane

Furukawa, Naoyuki,Kourogi, Noriko,Seki, Yoshio,Kakiuchi, Fumitoshi,Murai, Shinji

, p. 3764 - 3767 (2008/10/08)

The catalyzed reaction of an excess of styrene with n-Bu3GeH using several ruthenium and rhodium complexes gave the corresponding vinylgermanes (α-trin-butylgermylstyrene, (Z)-β-tri-n-butylgermylstyrene, and (E)-β-tri-n-butylgermylstyrene), whi

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