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Germane, (4-methoxyphenyl)trimethyl- is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

14476-81-4

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14476-81-4 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 14476-81-4 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 1,4,4,7 and 6 respectively; the second part has 2 digits, 8 and 1 respectively.
Calculate Digit Verification of CAS Registry Number 14476-81:
(7*1)+(6*4)+(5*4)+(4*7)+(3*6)+(2*8)+(1*1)=114
114 % 10 = 4
So 14476-81-4 is a valid CAS Registry Number.

14476-81-4SDS

SAFETY DATA SHEETS

According to Globally Harmonized System of Classification and Labelling of Chemicals (GHS) - Sixth revised edition

Version: 1.0

Creation Date: Aug 20, 2017

Revision Date: Aug 20, 2017

1.Identification

1.1 GHS Product identifier

Product name p-Me3GeC6H4OMe

1.2 Other means of identification

Product number -
Other names (4-Methoxy-phenyl)-trimethyl-germane

1.3 Recommended use of the chemical and restrictions on use

Identified uses For industry use only.
Uses advised against no data available

1.4 Supplier's details

1.5 Emergency phone number

Emergency phone number -
Service hours Monday to Friday, 9am-5pm (Standard time zone: UTC/GMT +8 hours).

More Details:14476-81-4 SDS

14476-81-4Relevant academic research and scientific papers

Mechanism and Selectivity of Aryltrimethylgermane Cation Radical Fragmentations

Feinberg, Elizabeth C.,Dinnocenzo, Joseph P.

, p. 8639 - 8644 (2020)

Aryltrimethylgermane cation radicals were generated by nanosecond transient absorption spectroscopy. Transient kinetics experiments show that the aryltrimethylgermane cation radicals react with added nucleophiles in reactions that are first-order in both

Palladium-Catalyzed Germylation of Aryl Bromides and Aryl Triflates Using Hexamethyldigermane

Komami, Narumi,Matsuoka, Keitaro,Yoshino, Tatsuhiko,Matsunaga, Shigeki

, p. 2067 - 2075 (2018/02/26)

Palladium-catalyzed germylation of aryl bromides and aryl triflates using commercially available hexamethyldigermane is described. Optimized reaction conditions afforded various functionalized aryltrimethylgermanes, including drug-like molecules, in moderate to good yields, demonstrating the versatility of the presented protocols.

SYNTHESIS AND SPECTROSCOPIC CHARACTERISTICS OF ARYLTRIMETHYL-SILICON, -GERMANIUM, AND -TIN COMPOUNDS

Moerlein, S. M.

, p. 29 - 40 (2007/10/02)

The synthesis and spectroscopic characteristics of 28 para-substituted aryltrimethyl-silicon, -germanium, and -tin compounds are described.The infrared spectra show characteristic bands at 1245-1165 (methyl bend), 840-765 (methyl rock), and 1105-1020 (in-plane aromatic H bend) cm-1; the frequency of the last band was found to depend on the sum of the aromatic substituent masses, the presence or absence of metallic constituents in the substituent having little influence.The mass spectral fragmentation patterns are interpreted in terms of localization of positive charge on the metal atom, with subsequent bond cleavage behavior which obeys the rules for mass spectra of carbon compounds.

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