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Methanone, phenylpyrazolo[1,5-a]pyridin-3-yl- is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

19364-00-2

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19364-00-2 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 19364-00-2 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 1,9,3,6 and 4 respectively; the second part has 2 digits, 0 and 0 respectively.
Calculate Digit Verification of CAS Registry Number 19364-00:
(7*1)+(6*9)+(5*3)+(4*6)+(3*4)+(2*0)+(1*0)=112
112 % 10 = 2
So 19364-00-2 is a valid CAS Registry Number.

19364-00-2SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 18, 2017

Revision Date: Aug 18, 2017

1.Identification

1.1 GHS Product identifier

Product name phenyl(pyrazolo[1,5-a]pyridin-3-yl)methanone

1.2 Other means of identification

Product number -
Other names phenyl-pyrazolo[1,5-a]pyridin-3-yl-methanone

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:19364-00-2 SDS

19364-00-2Relevant academic research and scientific papers

Gold/acid-co-catalyzed direct microwave-assisted synthesis of fused azaheterocycles from propargylic hydroperoxides

Alcaide, Benito,Almendros, Pedro,Quiros, M. Teresa

, p. 3384 - 3393 (2014/04/03)

The gold-acid-co-catalyzed synthesis of nine series of fused azaheterocycles with structural diversity starting from the same synthons as readily available propargylic hydroperoxides and aromatic amines has been achieved. The overall tandem process consists in a gold-catalyzed hydroperoxide rearrangement/Michael reaction followed by a final acid-catalyzed cyclization.

PYRAZOLOPYRIDINES. 1. FORMYLATION AND ACYLATION OF PYRAZOLOPYRIDINES

Tanji, Ken-ichi,Sasahara, Takehiko,Suzuki, Junko,Higashino, Takeo

, p. 915 - 924 (2007/10/02)

In the treatment of pyrazolopyridines with dimethylformamide and phosphorus oxychloride, Vilsmeier-Haack formylation proceeded at the 3-position, giving 3-pyrazolopyridinecarboxaldehydes.Reaction of the pyrazolopyridine with acyl hali

Acid-Catalyzed Reactions of 3-(α-Hydroxybenzyl)pyrazolopyridines

Hachiken, Hiroko,Takemura, Shoji,Ikeda, Masazumi

, p. 327 - 331 (2007/10/02)

Treatment of 3-(α-hydroxybenzyl)pyrazolopyridines with trifluoroacetic acid in dichloromethane resulted in the formation of pyrazolopyridines, bispyrid-3-yl)benzyl> ethers, and phenylbis(pyrazolopyrid-3-yl)methanes,

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