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Benzenediazonium, 2-methoxy-, chloride is a chemical compound with the molecular formula C7H8ClN3O. It is a derivative of benzenediazonium, featuring a methoxy group at the 2-position and a chloride ion as a counterion. Benzenediazonium, 2-methoxy-, chloride is an important intermediate in organic synthesis, particularly in the preparation of various dyes, pigments, and pharmaceuticals. It is known for its reactivity, as the diazonium group can undergo a range of chemical reactions, including coupling with phenols to form azo compounds. Due to its reactivity and potential to form explosive diazonium salts, it requires careful handling and storage. The compound is also characterized by its solubility in water and organic solvents, which can be useful in various chemical processes.

3425-23-8

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3425-23-8 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 3425-23-8 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 3,4,2 and 5 respectively; the second part has 2 digits, 2 and 3 respectively.
Calculate Digit Verification of CAS Registry Number 3425-23:
(6*3)+(5*4)+(4*2)+(3*5)+(2*2)+(1*3)=68
68 % 10 = 8
So 3425-23-8 is a valid CAS Registry Number.

3425-23-8SDS

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 2-methoxybenzenediazonium,chloride

1.2 Other means of identification

Product number -
Other names 2-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:3425-23-8 SDS

3425-23-8Upstream product

3425-23-8Relevant academic research and scientific papers

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

Curing accelerator, epoxy resin composition, and semiconductor device

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Page 16; 30, (2008/06/13)

A curing accelerator which is suitable for various curable resin compositions, an epoxy resin composition having excellent curability, storage stability and fluidity, and a semiconductor device having excellent solder cracking resistance and moisture resi

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.

Synthesis of novel tryptamine and azepinoindole derivatives

Novak, Lajos,Hanania, Michel,Kovacs, Peter,Rohaly, Janos,Kolonits, Pal,Szantay, Csaba

, p. 2331 - 2347 (2007/10/03)

A novel one-pot synthesis of azepinoindoles (9) via reaction of tryptamines (4) with formaldehyde is described. The scope and generality of this new procedure and the preparation of the starting compounds are also discussed.

Preparation of 7-methoxytryptamine

Soti,Incze,Kardos-Balogh,Kajtar-Peredy,Szantay

, p. 1689 - 1698 (2007/10/02)

7-Methoxytryptamine (6a) was prepared from cheap and easily available starting materials by using the Abramovitch-Shapiro method

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