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1,4-dihydroxy-2,5-di-(trimethylammonium iodide-methyl)phenyl is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

81926-14-9

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81926-14-9 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 81926-14-9 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 8,1,9,2 and 6 respectively; the second part has 2 digits, 1 and 4 respectively.
Calculate Digit Verification of CAS Registry Number 81926-14:
(7*8)+(6*1)+(5*9)+(4*2)+(3*6)+(2*1)+(1*4)=139
139 % 10 = 9
So 81926-14-9 is a valid CAS Registry Number.

81926-14-9Relevant academic research and scientific papers

Biological studies of photoinducible phenol quaternary ammonium derivatives

Song, Yang,Wang, Ping,Wu, Juanjuan,Zhou, Xiang,Zhang, Xiao-Lian,Weng, Linhong,Cao, Xiaoping,Liang, Feng

, p. 1660 - 1664 (2006)

Three water-soluble DNA cross-linking phenol quaternary ammonium derivatives 3, 4, and 5 could inhibit the transcription in vitro by photoactivation. DNA interstrand cross-linking action might be the key factor to inhibit transcription by these compounds.

A thiol-inducible and quick-response DNA cross-linking agent

Xu, Yuanzhen,Wei, Hongbo,Chen, Jianjun,Gao, Kun

supporting information, p. 281 - 283 (2018/11/27)

Three new 2,4-dinitrobenzenesulfonyl derivatives 1–3 were successfully prepared for the first time using a simple process. They were efficiently triggered by thiols (glutathione and L-cysteine) to release the corresponding phenol derivatives (4–6) within

Synthesis of Dihydrobenzofurans from Phenolic Mannich Bases and their Quaternized Derivatives

Blade-Font, Artur,Rocabayera, Teodoro de Mas

, p. 841 - 848 (2007/10/02)

Reaction of dimethylsulphoxonium methylide with quaternized derivatives of phenolic Mannich bases, and in certain cases with the bases themselves, constitutes a useful synthesis of dihydrobenzofurans.On the other hand treatment of those same quaternized derivatives with diazomethane may be a useful alternative procedure for the preparation of coumarans with base-sensitive groups.

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