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Benzenediazonium, 4-ethyl-, chloride is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

41888-23-7

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41888-23-7 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 41888-23-7 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 4,1,8,8 and 8 respectively; the second part has 2 digits, 2 and 3 respectively.
Calculate Digit Verification of CAS Registry Number 41888-23:
(7*4)+(6*1)+(5*8)+(4*8)+(3*8)+(2*2)+(1*3)=137
137 % 10 = 7
So 41888-23-7 is a valid CAS Registry Number.

41888-23-7SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 14, 2017

Revision Date: Aug 14, 2017

1.Identification

1.1 GHS Product identifier

Product name 4-ethylbenzenediazonium,chloride

1.2 Other means of identification

Product number -
Other names Benzenediazonium,4-ethyl-,chloride

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:41888-23-7 SDS

41888-23-7Upstream product

41888-23-7Relevant academic research and scientific papers

Synthesis, characterization, and electrochemical study of some novel, azo-containing Schiff bases and their Ni(II) complexes

Menati, Saeid,Azadbakht, Azadeh,Azadbakht, Reza,Taeb, Abbas,Kakanejadifard, Ali

, p. 499 - 506 (2013/07/27)

Five novel azo-azomethine ligands with NN'OS coordination spheres were prepared by reaction of methyl-2-{N-(2′-aminoethane)}-amino-1- cyclopentenedithiocarboxylate (Hcden) with (E)-2-hydroxy-5-(phenyldiazenyl) benzaldehyde and its substituted derivatives

Di-substituted azocalix[4]arenes containing chromogenic groups: Synthesis, characterization, extraction, and thermal behavior

El?in, Serkan,Delig?z, Hasalettin

, p. 6832 - 6838 (2013/07/26)

In this study, the synthesis of chromogenic di-substituted azocalix[4]arene derivatives is described. Six novel azocalix[4]arenes (4a-f)were prepared by linking 4-methoxy, 4-methyl, 4-ethyl, 4-chloro, 4-bromo, and 4-nitroaniline to 25,26,27,28-tetrahydrox

Synthesis and Pharmacology of Some New Oxime Ethers Derived from 2-Acetyl-5-arylthiophenes

Shridhar, D. R.,Sastry, C. V. Reddy,Chaturvedi, S. C.,Gurumurthy, R.,Singh, P. P.,et al.

, p. 692 - 694 (2007/10/02)

Several new 5-arylthiophene-2-acetoxime ethers (1-28) have been synthesised and screened for their pharmacological activities.Some of these compounds possess moderate antiinflammatory and mild CNS depressant activities.The intermediate 2-acetyl-5-(p-ethyl/p-iso-propyl/3,4-dimethylphenyl)thiophenes (1b-d) and their oximes (IIb-d) have been reported for the first time.

Substituent Effects on 13C and 15N Chemical Shifts in Triazenes Studied by Principal Components Multivariate Data Analysis

Dunn, III, W.J.,Lins, C.,Kumar, G.,Manimaran, T.,Grigoras, S.,et al.

, p. 450 - 456 (2007/10/02)

Principal components analysis was applied to the 13C and 15N chemical shift data on a series of fifteen 1-(para-substituted-phenyl)-3-acetyl-3-methyltriazenes.It was found that the halogen-substituted triazenes formed a class, based on substituent effects, which was different from the remaining eleven triazenes.A one-component model described the halogen class, whereas a two-component model was necessary for a description of the second class.In the second class, substituent tended to cluster to form groups depending on their electronic character.

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