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22934-41-4

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22934-41-4 Usage

Uses

Quinoline-5-carboxaldehyde is used as a precursor in the preparation of pharmaceuticals.

Check Digit Verification of cas no

The CAS Registry Mumber 22934-41-4 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 2,2,9,3 and 4 respectively; the second part has 2 digits, 4 and 1 respectively.
Calculate Digit Verification of CAS Registry Number 22934-41:
(7*2)+(6*2)+(5*9)+(4*3)+(3*4)+(2*4)+(1*1)=104
104 % 10 = 4
So 22934-41-4 is a valid CAS Registry Number.
InChI:InChI=1/C10H7NO/c12-7-8-3-1-5-10-9(8)4-2-6-11-10/h1-7H

22934-41-4 Well-known Company Product Price

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  • (Code)Product description
  • CAS number
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  • Alfa Aesar

  • (L19641)  Quinoline-5-carboxaldehyde, 97+%   

  • 22934-41-4

  • 250mg

  • 658.0CNY

  • Detail
  • Alfa Aesar

  • (L19641)  Quinoline-5-carboxaldehyde, 97+%   

  • 22934-41-4

  • 1g

  • 1828.0CNY

  • Detail
  • Alfa Aesar

  • (L19641)  Quinoline-5-carboxaldehyde, 97+%   

  • 22934-41-4

  • 5g

  • 7036.0CNY

  • Detail

22934-41-4SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 18, 2017

Revision Date: Aug 18, 2017

1.Identification

1.1 GHS Product identifier

Product name quinoline-5-carbaldehyde

1.2 Other means of identification

Product number -
Other names 5-Formylquinoline

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:22934-41-4 SDS

22934-41-4Relevant articles and documents

MALT1 MODULATORS AND USES THEREOF

-

Paragraph 00120; 00164, (2021/07/10)

Provided herein are compounds, compositions, and methods useful for modulating MALT1 and for treating related diseases, disorders, and conditions.

N-aryl(thio)anthranilic acid amide derivatives, their preparation and their use as VEGF receptor tyrosine kinase inhibitors

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, (2008/06/13)

Described are compounds of formula (I), wherein W is O or S; X is NR8; Y is CR9R10-(CH2)n wherein R9 and R10 are independently of each other hydrogen or lower alkyl, and n is an integer of

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