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98549-88-3

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  • China Northwest Largest Factory Manufacturer Supply 1H-PYRROLO[2,3-B]PYRIDIN-5-OL CAS 98549-88-3

    Cas No: 98549-88-3

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98549-88-3 Usage

Chemical Properties

Light yellow solid

Uses

1H-?Pyrrolo[2,?3-?b]?pyridin-?5-?ol is a reagent used in the synthesis of potent VEGFR-2 inhibitors. 7-Azaindole derivative identified as an intermediate in the synthesis of Venetoclax (A112430), a potent and selective BCL-2 inhibitor that achieves potent antitumour activity while sparing platelets.

Check Digit Verification of cas no

The CAS Registry Mumber 98549-88-3 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 9,8,5,4 and 9 respectively; the second part has 2 digits, 8 and 8 respectively.
Calculate Digit Verification of CAS Registry Number 98549-88:
(7*9)+(6*8)+(5*5)+(4*4)+(3*9)+(2*8)+(1*8)=203
203 % 10 = 3
So 98549-88-3 is a valid CAS Registry Number.
InChI:InChI=1/C7H6N2O/c10-6-3-5-1-2-8-7(5)9-4-6/h1-4,10H,(H,8,9)

98549-88-3 Well-known Company Product Price

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  • Aldrich

  • (ADE000886)  1H-Pyrrolo[2,3-b]pyridin-5-ol  AldrichCPR

  • 98549-88-3

  • ADE000886-1G

  • 7,411.95CNY

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98549-88-3SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 12, 2017

Revision Date: Aug 12, 2017

1.Identification

1.1 GHS Product identifier

Product name 1H-Pyrrolo[2,3-b]pyridin-5-ol

1.2 Other means of identification

Product number -
Other names 1H-PYRROLO[2,3-B]PYRIDIN-5-OL

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

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Service hours Monday to Friday, 9am-5pm (Standard time zone: UTC/GMT +8 hours).

More Details:98549-88-3 SDS

98549-88-3Upstream product

98549-88-3Relevant articles and documents

Synthesis of functionalized 7-azaindoles via directed ortho-metalations

L'Heureux, Alexandre,Thibault, Carl,Ruel, Réjean

, p. 2317 - 2319 (2007/10/03)

Functionalization at C-5 of 4-fluoro- and 4-chloro-1-triisopropylsilyl-7- azaindole, 1 and 2, respectively, leads to a variety of new substituted 7-azaindole derivatives. We also describe two approaches to introduce functionality at C-6.

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