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2-Bromo-3-Methyl-4-Pyridinamine is a chemical compound with the molecular formula C6H7BrN2. It belongs to the class of organic compounds called pyridines and derivatives. Pyridines are compounds containing a pyridine ring, a six-membered aromatic heterocycle which consists of one nitrogen atom and five carbon atoms. The specific properties of 2-Bromo-3-Methyl-4-Pyridinamine, including its reactivity and biological activity, largely depend on its particular molecular structure.

79055-61-1

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79055-61-1 Usage

Uses

Used in Pharmaceutical and Chemical Research:
2-Bromo-3-Methyl-4-Pyridinamine is used as a building block for the synthesis of more complex molecules. Its unique molecular structure allows it to be a valuable component in the development of new drugs and other chemical compounds.
Used in Chemical Reactions:
2-Bromo-3-Methyl-4-Pyridinamine is used as a reactant in various chemical reactions. Its reactivity makes it a useful compound for creating new molecules and advancing chemical research.

Check Digit Verification of cas no

The CAS Registry Mumber 79055-61-1 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 7,9,0,5 and 5 respectively; the second part has 2 digits, 6 and 1 respectively.
Calculate Digit Verification of CAS Registry Number 79055-61:
(7*7)+(6*9)+(5*0)+(4*5)+(3*5)+(2*6)+(1*1)=151
151 % 10 = 1
So 79055-61-1 is a valid CAS Registry Number.

79055-61-1SDS

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-bromo-3-methylpyridin-4-amine

1.2 Other means of identification

Product number -
Other names 2-Bromo-3-methyl-4-pyridinamine

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:79055-61-1 SDS

79055-61-1Downstream Products

79055-61-1Relevant academic research and scientific papers

Substituted-3H-imidazo[4,5-c]pyridine and 1H-pyrrolo[2,3-c]pyridine series of novel Ectonucleotide Pyrophosphatase/Phosphodiesterase-1 (ENPP1) and Stimulator for Interferon Genes (STING) modulators as cancer immunotherapeutics

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, (2020/02/19)

Substituted -3H-imidazo[4,5-c]pyridine and 1H-pyrrolo[2,3-c]pyridine series of novel Ectonucleotide Pyrophosphatase/Phosphodiesterase-1 (ENPP1) and related compounds, which are useful as inhibitors of ENPP1; synthetic methods for making the compounds; pharmaceutical compositions comprising the compounds; and methods of using the compounds and compositions to treat disorders associated with dysfunction of the ENPP1.

Technological method for preparing 2- amino -6-5-methyl-substituted-pyridine (by machine translation)

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Paragraph 0061-0085, (2020/01/12)

The reaction solvent of 2 - the method is reacted in a reaction solvent under the action, of 2 - an, acid anhydride and an acid,binding, agent and an amination reagent under the action. of an acid anhydride and 2 - an acid-binding agent and, an amination reagent, 2 -4 - 93/7, 99.8%, 70%. (by machine translation)

PROCESS FOR PREPARATION OF LUMACAFTOR

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, (2017/05/07)

The present invention relates to a process for the preparation of amorphous lumacaftor. The present invention relates to a process for the preparation of intermediate 6-amino-2- halo-3-methylpyridine compounds used in the preparation of lumacaftor. The present invention relates to lumacaftor hydrobromide, process for its preparation and conversion thereof to lumacaftor.

SOLID FORMS OF LUMACAFTOR, ITS SALTS AND PROCESSES THEREOF

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Page/Page column 51-52, (2017/11/04)

Aspects of the present application relate to solid forms of Lumacaftor, its salts and processes thereof. Specific aspects of the present application relate to alternate processes for the preparation of Lumacaftor and intermediates thereof. Present application further relates to the solid forms of Lumacaftor and its salts.

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