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148680-52-8

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148680-52-8 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 148680-52-8 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,4,8,6,8 and 0 respectively; the second part has 2 digits, 5 and 2 respectively.
Calculate Digit Verification of CAS Registry Number 148680-52:
(8*1)+(7*4)+(6*8)+(5*6)+(4*8)+(3*0)+(2*5)+(1*2)=158
158 % 10 = 8
So 148680-52-8 is a valid CAS Registry Number.

148680-52-8SDS

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 5-[[4-(4-fluorophenyl)piperazin-1-yl]methyl]-2-phenyl-3,3a-dihydropyrazolo[1,5-d][1,2,4]triazin-4-one

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:148680-52-8 SDS

148680-52-8Downstream Products

148680-52-8Relevant articles and documents

Synthesis of new 5-substituted pyrazolo[1,5-d][1,2,4]triazine derivatives and their analgesic, anti-inflammatory and antipyretic properties

Mavel,Rubat,Coudert,Privat,Couquelet,Tronche,Bastide

, p. 464 - 468 (2007/10/02)

A series of 2-aryl-4-oxo-pyrazolo[1,5-d][1,2,4]triazines substituted in the 5-position by aminoalkyl or benzoyl moieties was synthesized and evaluated for analgesic activity. The structures of new triazine derivatives were confirmed by IR, 1H-NMR spectra and by elementary analysis. In the phenylbenzoquinone induced writhing test, only 3,3a-dihydropyrazolo triazines substituted by an arylpiperazinylmethyl group exhibited potent analgesic effect. In addition, these compounds possessed significant anti-inflammatory and antipyretic properties. A desaturation in 3,3a positions or other groups than arylpiperazinylmethyl moieties notably decreased analgesic effects.

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