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1H-Pyrazole-4-carboxaldehyde, 5-chloro-1-phenyl-3-(4-pyridinyl)- is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

848355-70-4

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848355-70-4 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 848355-70-4 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 8,4,8,3,5 and 5 respectively; the second part has 2 digits, 7 and 0 respectively.
Calculate Digit Verification of CAS Registry Number 848355-70:
(8*8)+(7*4)+(6*8)+(5*3)+(4*5)+(3*5)+(2*7)+(1*0)=204
204 % 10 = 4
So 848355-70-4 is a valid CAS Registry Number.

848355-70-4SDS

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 5-chloro-1-phenyl-3-pyridin-4-yl-1H-pyrazole-4-carbaldehyde

1.2 Other means of identification

Product number -
Other names -

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:848355-70-4 SDS

848355-70-4Relevant academic research and scientific papers

A convenient synthesis of some pyrazolinone and pyrazole derivatives

Aly, El-Saied A.,Abdo, Mohamed A.,El-Gharably, Atif A.

, p. 983 - 990 (2007/10/03)

A convenient synthesis of some novel 6-amino-4-aryl-1-phenyl-3-pyridin-4- yl-1,4-dihydropyrano[2,3-c]pyrazole-5-carbonitriles (3a,b) and 5-chloro-1-phenyl-3-pyridin-4-yl-1H-pyrazole-4-carbaldehyde (4) is described. Compound 4 was obtained by the reaction of 2-phenyl-5-pyridin-4-yl-2,4- dihydropyrazol-3-one (1) with dimethylformamide and phosphorus oxychloride under Vilsmeier-Haack reaction conditions. Compound 4 was subjected to react with different reagents such as hippuric acid, sodium azide and aromatic ketones to afford 4-(5-chloro-1-phenyl-3-pyridin-4-yl-1H-pyrazolo-4-ylmethylene)-2-phenyl-4 H-oxazol-5-one(5), 5-azido-1-phenyl-3-pyridin-4-yl-1H-pyrazol-4-carbaldehyde (8) and 1-aryl-3-(5-chloro-1-phenyl-3-pyridin-4-yl-1H-pyrazol-4-yl)propenones (12a,b), respectively. The latter compounds were also prepared via Michael reaction by treatment of compound 1 with some different chalcones.

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