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M-tolyltribromogermane is an organogermanium compound with the chemical formula C7H7GeBr3. It is a derivative of toluene, where one hydrogen atom is replaced by a tribromogermanium group. m-tolyltribromogermane is characterized by its potential applications in various fields, such as organic synthesis and materials science. M-tolyltribromogermane is known for its unique reactivity and stability, which can be attributed to the presence of the heavy germanium atom and the electron-withdrawing bromine atoms. Due to its specific chemical properties, it has been studied for its potential use in the synthesis of more complex organogermanium compounds and as a precursor in the development of new materials with unique electronic and optical properties.

6181-09-5

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6181-09-5 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 6181-09-5 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 6,1,8 and 1 respectively; the second part has 2 digits, 0 and 9 respectively.
Calculate Digit Verification of CAS Registry Number 6181-09:
(6*6)+(5*1)+(4*8)+(3*1)+(2*0)+(1*9)=85
85 % 10 = 5
So 6181-09-5 is a valid CAS Registry Number.

6181-09-5Upstream product

6181-09-5Downstream Products

6181-09-5Relevant academic research and scientific papers

Synthesis and molecular structure of phenyl and tolylgermatranes

Lukevics, Edmunds,Ignatovich, Luba,Belyakov, Sergey

, p. 222 - 230 (1999)

The crystals of arylgermatranes (R=H (I), 4-CH3 (II), 3-CH3 (III), 2-CH3 (IV)), have been obtained to study the influence of a substituent position on coordination of the germanium atom. Compounds I-IV were prepared by the insertion of GeBr2 into the carbon-bromine bond of the corresponding arylbromide, conversion of aryltribromogermanes to triethoxy derivatives by alcoholysis and their transalkoxylation with triethanolamine to germatranes; or by the condensation of halobenzene with GeCl4 in the presence of copper powder followed by alcoholysis and cyclization. The crystal structure of compounds I-IV was studied via the X-ray diffraction method. The intramolecular donor-acceptor bond Ge←N in arylgermatranes (2.212-2.230 A) is longer than that in the corresponding furyl- and thienylgermatranes. Introduction of a substituent into o-position of the benzene ring decreases the N-Ge-C angle value from 177.5 to 144.2°. The quantum chemical calculations were performed to investigate structures I-IV in isolated molecules.

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