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19363-99-6

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19363-99-6 Usage

Uses

Mostly used in the suzuki coupling reaction.

Check Digit Verification of cas no

The CAS Registry Mumber 19363-99-6 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 3 respectively; the second part has 2 digits, 9 and 9 respectively.
Calculate Digit Verification of CAS Registry Number 19363-99:
(7*1)+(6*9)+(5*3)+(4*6)+(3*3)+(2*9)+(1*9)=136
136 % 10 = 6
So 19363-99-6 is a valid CAS Registry Number.

19363-99-6 Well-known Company Product Price

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  • Alfa Aesar

  • (H35255)  3-Iodopyrazolo[1,5-a]pyridine, 97%   

  • 19363-99-6

  • 250mg

  • 1263.0CNY

  • Detail
  • Alfa Aesar

  • (H35255)  3-Iodopyrazolo[1,5-a]pyridine, 97%   

  • 19363-99-6

  • 1g

  • 3788.0CNY

  • Detail

19363-99-6SDS

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 3-iodopyrazolo[1,5-a]pyridine

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:19363-99-6 SDS

19363-99-6Relevant articles and documents

INHIBITORS OF CYCLIN-DEPENDENT KINASES

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Paragraph 00287, (2021/02/12)

Provided herein are compounds which are inhibitors of cyclin-dependent kinases (CDKs), pharmaceutical compositions comprising said compounds, and methods for using said compounds for the treatment of diseases.

PHARMACEUTICALS COMPRISING BIARYL DERIVATIVES OR SALTS THEREOF

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Paragraph 0217; 0218; 0219, (2018/10/24)

PROBLEM TO BE SOLVED: To provide compounds with excellent antimycotic activity against Trichophyton. SOLUTION: The invention provides pharmaceuticals comprising biaryl derivatives represented by general formula (I) or salts thereof, where ring A is optionally substituted phenyl or the like; Q is CH2 or the like; X1, X2 and X3 are CR1 or the like; and Y is CH or N. SELECTED DRAWING: None COPYRIGHT: (C)2018,JPOandINPIT

Optimized scale up of 3-pyrimidinylpyrazolo[1,5-a]pyridine via Suzuki coupling; A general method of accessing a range of 3-(hetero)arylpyrazolo[1,5-a] pyridines

Bethel, Paul A.,Campbell, Andrew D.,Goldberg, Frederick W.,Kemmitt, Paul D.,Lamont, Gillian M.,Suleman, Abid

experimental part, p. 5434 - 5444 (2012/09/08)

We have developed an improved synthesis of 3-(hetero)aryl pyrazolo[1,5-a]pyridines (such as 3-(2,5-dichloropyrimidin-4-yl)pyrazolo[1,5-a] pyridine (8)) via an optimized synthesis and Suzuki coupling of 3-pyrazolo[1,5-a]pyridine boronic ester 10. These conditions are applicable to both high throughput chemistry and large scale synthesis of these medicinally important compounds. The scope of this chemistry has been further extended to include the synthesis and coupling of a novel boronic ester, 3-(4,4,5,5-tetramethyl-1,3,2-dioxaborolan-2-yl)-6,7-dihydro-5H-pyrazolo[5,1-b] [1,3]oxazine (43).

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