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Benzenediazonium, 3,4-dimethyl-, chloride is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

69457-08-5

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69457-08-5 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 69457-08-5 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 6,9,4,5 and 7 respectively; the second part has 2 digits, 0 and 8 respectively.
Calculate Digit Verification of CAS Registry Number 69457-08:
(7*6)+(6*9)+(5*4)+(4*5)+(3*7)+(2*0)+(1*8)=165
165 % 10 = 5
So 69457-08-5 is a valid CAS Registry Number.

69457-08-5SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 13, 2017

Revision Date: Aug 13, 2017

1.Identification

1.1 GHS Product identifier

Product name 3,4-dimethylbenzenediazonium,chloride

1.2 Other means of identification

Product number -
Other names 3,4-Dimethyl-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:69457-08-5 SDS

69457-08-5Upstream product

69457-08-5Relevant academic research and scientific papers

Synthesis of new 1-(3,4-dimethylphenyl)-1,5-dihydropyrazolo[3,4-d]pyrimidin-4-one derivatives

Zhidkov,Kutkin,Fetisova,Zverev,Zaraeva,Gorokhov,Chubarova

, p. 592 - 598 (2017/06/06)

New substituted pyrazolo[3,4-d]pyrimidin-4-ones have been synthesized as a result of a series of transformations including hydrolysis of ethyl 5-amino-1H-pyrazole-4-carboxylates, cyclization of the carboxylic acids thus obtained to pyrazolo[3,4-d][1,3]oxazin-4(1H)-ones, and treatment of the latter with substituted anilines. The final pyrazolo[3,4-d]pyrimidin-4-one derivatives can also be synthesized from 5-(arylamido)-1H-pyrazole-4-carboxylic acids in the presence of a catalytic amount of anhydrous zinc(II) chloride.

Synthesis and antimicrobial activity of 2-(4-formyl-3-pyrazolyl)-3- phenylindoles

Maddirala, Shambabu Joseph,Gokak, Vidya S.,Basanagoudar, Linganagouda D.

, p. 2410 - 2415 (2007/10/03)

Vilsmeier-Haack reagent (POCl3-DMF) on reaction with hydrazones 3a-i derived from 2-acetyl-3-phenylindoles 2a-c furnishes 2-(4-formyl-3- pyrazolyl)-3-phenylindoles 4a-i. The structures of these compounds have been established on the basis of their elemental analyses and spectral (IR, 1H NMR) data. All the pyrazole derivatives 4a-i and their azines 5a-i have been tested for their antimicrobial and antifungal activities.

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.

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