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153888-47-2

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153888-47-2 Usage

Uses

Methyl 5-bromo-1-methyl-6-oxo-1,6-dihydropyridine-3-carboxylate is a starting material in the synthesis of Functionalized Tricyclic Pyrrolo-Pyridones

Check Digit Verification of cas no

The CAS Registry Mumber 153888-47-2 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,5,3,8,8 and 8 respectively; the second part has 2 digits, 4 and 7 respectively.
Calculate Digit Verification of CAS Registry Number 153888-47:
(8*1)+(7*5)+(6*3)+(5*8)+(4*8)+(3*8)+(2*4)+(1*7)=172
172 % 10 = 2
So 153888-47-2 is a valid CAS Registry Number.

153888-47-2SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 12, 2017

Revision Date: Aug 12, 2017

1.Identification

1.1 GHS Product identifier

Product name methyl 5-bromo-1-methyl-6-oxopyridine-3-carboxylate

1.2 Other means of identification

Product number -
Other names methyl 5-bromo-1-methyl-6-oxo-1,6-dihydro-3-pyridinecarboxylate

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:153888-47-2 SDS

153888-47-2Relevant articles and documents

Expeditious Access to Functionalized Tricyclic Pyrrolo-Pyridones via Tandem or Sequential C-N/C-C Bond Formations

Fillery, Shaun M.,Gregson, Clare L.,Guérot, Carine M.

, p. 9128 - 9132 (2019)

The facile synthesis of both saturated and unsaturated tricyclic pyrrolo-pyridones starting from a single readily available, common monocyclic reagent has been developed. An intermolecular annulation via a tandem Buchwald-Hartwig/Heck reaction led to the synthesis of β-carbolinones. The analogous semisaturated tricyclic pyrrolo-pyridones were prepared in good to excellent yields by sequential Buchwald-Hartwig and Fischer indole reactions. The methods feature mild reaction conditions and good functional group tolerance.

PCSK9 INHIBITORS AND METHODS OF USE THEREOF

-

, (2020/07/31)

The invention relates to a novel inhibitor pharmacophore of PCSK9 and heteroaryl compounds that bind the PCSK9 protein.

PYRIDINYL BASED APOPTOSIS SIGNAL-REGULATION KINASE INHIBITORS

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Paragraph 0543, (2018/09/12)

Apoptosis signal-regulating kinase 1 (ASK1) activation and signaling have been reported to play an important role in a broad range of diseases including neurodegenerative, cardiovascular, inflammatory, autoimmunity and metabolic disorders. Disclosed herein is the synthesis of pyridinyl derived therapeutic agents that function as inhibitors of ASK 1 as well as their pharmaceutical compositions and methods of use.

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