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Benzenediazonium, 3-methoxy-, chloride is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

19183-05-2

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19183-05-2 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 19183-05-2 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 1,9,1,8 and 3 respectively; the second part has 2 digits, 0 and 5 respectively.
Calculate Digit Verification of CAS Registry Number 19183-05:
(7*1)+(6*9)+(5*1)+(4*8)+(3*3)+(2*0)+(1*5)=112
112 % 10 = 2
So 19183-05-2 is a valid CAS Registry Number.

19183-05-2SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 16, 2017

Revision Date: Aug 16, 2017

1.Identification

1.1 GHS Product identifier

Product name 3-methoxybenzenediazonium,chloride

1.2 Other means of identification

Product number -
Other names 3-Methoxy-benzoldiazonium,Chlorid

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:19183-05-2 SDS

19183-05-2Relevant academic research and scientific papers

(E)-N-Aryl-2-oxo-2-(3,4,5-trimethoxyphenyl)acetohydrazonoyl cyanides as tubulin polymerization inhibitors: Structure-based bioisosterism design, synthesis, biological evaluation, molecular docking and in silico ADME prediction

Wang, Guangcheng,Peng, Zhiyun,Peng, Shanshan,Qiu, Jie,Li, Yongjun,Lan, Yanyu

supporting information, p. 3350 - 3355 (2018/09/12)

A series of (E)-N-Aryl-2-oxo-2-(3,4,5-trimethoxyphenyl)acetohydrazonoyl cyanides have been synthesized and evaluated for their anticancer activity in human hepatocellular liver carcinoma HepG2 and breast adenocarcinoma MCF-7 cell lines. Among all the test

Synthetic method of substituted phenyl diazene compound and application of synthetic method

-

Paragraph 0133; 0134, (2017/06/02)

The invention relates to a novel synthetic method of a substituted phenyl diazene compound and an application of the synthetic method. The substituted phenyl diazene compound is obtained through reduction of substituted phenyl diazonium salt; a reducing a

Synthesis method of substituted phenylhydrazine and salt thereof

-

Paragraph 0133; 0134, (2017/08/29)

The invention relates to a novel synthesis method of substituted phenylhydrazine and salt thereof. A substituted phenyl diazene compound is reduced to generate the substituted phenylhydrazine; a reducing agent B is selected from one or several of a catalytic hydrogenating system, formic acid, formate and formic acid ester compound; the obtained substituted phenylhydrazine can be further acidified to prepare the substituted phenylhydrazine salt which is easily stored and transported. The synthesis method has the advantages that the yield rate is high, the cost is low, the reaction time is short, the technology operation and post-treatment are simple, and the amount of waste water, waste gas and waste residue is fewer; the component of the produced waste water is single, the recycling is convenient, the treatment cost is low, and the green chemical requirement is met; the synthesis method of the substituted phenylhydrazine is more suitable for the large-scale industrialized production.

New fluorescent symmetrically substituted perylene-3,4,9,10-dianhydride- azohybrid dyes: Synthesis and spectroscopic studies

Saeed, Aamer,Shabir, Ghulam

, p. 7 - 12 (2014/06/24)

Five phenolic azo-dyes (3a-e) were synthesized by diazo coupling of the suitably substituted anilines (1a-e) with phenol at low temperature in alkaline medium. The resulting dyes have low solubility in aqueous medium due to lack of carboxylic or sulfonic

Parallel synthesis of "Click" chalcones as antitubulin agents

Utsintong, Maleeruk,Massarotti, Alberto,Caldarelli, Antonio,Theeramunkong, Sewan

, p. 510 - 516 (2013/07/28)

It has been shown that some chalcones are able to inhibit tubulin polymerization, giving cytotoxicity and destruction of tumoral vasculature. A library of 180 novel chalcone analogs has been synthesized via click chemistry and screened for their cytotoxic

Aromatic heterocyclic derivatives as enzyme inhibitors

-

Page column 124, (2010/02/04)

The present invention discloses peptide aldehydes which are potent and specific inhibitors of thrombin, their pharmaceutically acceptable salts, pharmaceutically acceptable compositions thereof, and methods of using them as therapeutic agents for disease states in mammals characterized by abnormal thrombosis.

Reaction of Triazene 1-Oxides: Novel Synthesis of Solid Arenediazonium Chlorides

Mohamed, Shaaban K.,Gomaa, Mohsen A.-M.,Nour El-Din, Ahmed M.

, p. 166 - 167 (2007/10/03)

Treatment of 1,3-diaryltriazene 1-oxides with oxalyl chloride in dry toluene at room temperature gives only solid arenediazonium chlorides; however, treatment with acetyl and benzoyl chlorides does not afford the corresponding diazonium chlorides.

FORMATION OF ARENEDIAZONIUM ION IN OXIDATION OF N,N-DIMETHYL-4-AMINOBENZENE AND SOME meta-SUBSTITUTED DERIVATIVES WITH CERIMU(IV) ION IN ACID MEDIUM

Matrka, Miroslav,Pipalova, Jitka

, p. 2711 - 2715 (2007/10/02)

Oxidation has been studied of an experimental hepatocarcinogene N,N-dimethyl-4-aminoazobenzene and some its meta-substituted derivatives with cerium(IV) ion in 1M hydrochloric acid medium with potentiometric indication.It has been possible to prove format

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