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69898-42-6

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69898-42-6 Usage

Synonyms

BMS-690514

Molecular Class

Pyridinecarboxylic acids

Derivation

Derived from indole and pyridine moieties

Potential Applications

Therapeutic uses, particularly as a kinase inhibitor for targeted cancer treatment

Mechanism of Action

Inhibition of specific kinases involved in cell proliferation and survival

Status

Requires further research and clinical trials to validate its therapeutic potential

Check Digit Verification of cas no

The CAS Registry Mumber 69898-42-6 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 6,9,8,9 and 8 respectively; the second part has 2 digits, 4 and 2 respectively.
Calculate Digit Verification of CAS Registry Number 69898-42:
(7*6)+(6*9)+(5*8)+(4*9)+(3*8)+(2*4)+(1*2)=206
206 % 10 = 6
So 69898-42-6 is a valid CAS Registry Number.
InChI:InChI=1/C18H16N2O3/c1-3-20-11(2)15(12-7-4-5-9-14(12)20)17(21)16-13(18(22)23)8-6-10-19-16/h4-10H,3H2,1-2H3,(H,22,23)

69898-42-6SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 15, 2017

Revision Date: Aug 15, 2017

1.Identification

1.1 GHS Product identifier

Product name 2-[(1-ethyl-2-methyl-3-indolyl)carbonyl]-3-pyridinecarboxylic acid

1.2 Other means of identification

Product number -
Other names 1-ethyl-2-methylindol-3-yl 3-carboxypyridin-2-yl ketone

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:69898-42-6 SDS

69898-42-6Upstream product

69898-42-6Relevant articles and documents

Substituted furopyridinones and furopyrazinones

-

, (2008/06/13)

Substituted furopyridinones and furopyrazinones which are useful as color formers in pressure-sensitive carbonless duplicating systems and thermal marking systems are prepared by reacting diphenylamines with substituted benzoyl (or 3-indolylcarbonyl)pyridinecarboxylic acids and substituted benzoyl (or 3-indolylcarbonyl)pyrazinecarboxylic acids, respectively.

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