59047-70-0

Basic information

• Product Name: (2-CHLORO-PYRIDIN-4-YL)-DIMETHYL-AMINE
• Synonyms: (2-CHLORO-PYRIDIN-4-YL)-DIMETHYL-AMINE;2-Chloro-4-(dimethylamino)pyridine;2-chloro-N,N-dimethylpyridin-4-amine
• CAS NO: 59047-70-0
• Molecular Formula: C₇H₉ClN₂
• Molecular Weight: 156.61276
• Mol File: 59047-70-0.mol
• Article Data: 5

Chemical Properties

• Appearance: /
• CAS DataBase Reference: (2-CHLORO-PYRIDIN-4-YL)-DIMETHYL-AMINE(CAS DataBase Reference)
• NIST Chemistry Reference: (2-CHLORO-PYRIDIN-4-YL)-DIMETHYL-AMINE(59047-70-0)
• EPA Substance Registry System: (2-CHLORO-PYRIDIN-4-YL)-DIMETHYL-AMINE(59047-70-0)

Safety Data

• Hazardous Substances Data: 59047-70-0(Hazardous Substances Data)

Usage

General Description

(2-Chloro-pyridin-4-yl)-dimethyl-amine is a chemical compound with the molecular formula C7H9ClN2. It is a derivative of pyridine and contains a chloro substituent at the 2-position and a dimethylamino group attached to the 4-position of the pyridine ring. (2-CHLORO-PYRIDIN-4-YL)-DIMETHYL-AMINE has applications in the pharmaceutical and agrochemical industries, including its use as an intermediate in the synthesis of various pharmaceutical agents. It is also used in the production of pesticides and other agrochemical products. Additionally, (2-Chloro-pyridin-4-yl)-dimethyl-amine may have potential uses in research and development as a building block for the creation of new chemical compounds with diverse properties and applications.

Upstream product

• 26452-80-2 2,4-dichloropyridine 
• 124-40-3 dimethyl amine 
• 73583-37-6 2-chloro-4-bromopyridine 
• 506-59-2 N,N-dimethylammonium chloride 
• 837365-03-4 2,4-dichloro-6-hydrazinopyridine 
• 98027-84-0 2,6-dichloro-4-iodopyridine 
• 16063-69-7 2,4,6-trichloropyridine 
• 2402-78-0 2,6-dichloropyridine 
• 837365-00-1 2,4,6-trichloro-3-(trimethylsilyl)pyridine 
• 1122-58-3 dmap 

Downstream Products

• 1421748-75-5 C₂₇H₄₂N₄O₃S 
• 1421748-74-4 C₂₃H₃₈N₄O₃S 
• 1421748-73-3 C₂₃H₃₆N₄O₃S 
• 1421748-72-2 C₂₈H₄₃N₅O₄S 
• 1421748-71-1 C₂₂H₃₁N₅O₄S 
• 1421748-70-0 C₂₈H₄₄N₄O₂S 
• 1421748-69-7 C₂₂H₃₂N₄O₂S 
• 1421748-68-6 C₂₀H₂₈N₄O₂S 
• 1421748-67-5 C₁₄H₂₁F₃N₄O₂S 
• 1421748-66-4 C₁₄H₂₄N₄O₂S 
• 1416450-11-7 N²,N²'-((1R,2R)-cyclohexane-1,2-diyl)bis(N⁴,N⁴-dimethylpyridine-2,4-diamine) 
• 1421748-76-6 1-(3,5-bis(trifluoromethyl)phenyl)-3-((1R,2R)-2-((4-(dimethylamino)pyridin-2-yl)amino)cyclohexyl)thiourea 
• 85698-56-2 N⁴,N⁴,N^4',N^4'-tetramethyl-[2,2'-bipyridine]-4,4'-diamine 
• 1290059-15-2 2-chloro-6-(cyclohex-2-en-1-yl)-N,N-dimethylpyridin-4-amine 

Relevant articles and documents

PYRAZOLOPYRIMIDIN-2-YL DERIVATIVES AS JAK INHIBITORS

New pyrazolopyridmiin-2-yl derivatives are disclosed; as well as process for their preparation, pharmaceutical compositions comprising them and their use in therapy as inhibitors of Janus Kinases (JAK).

DIARYLAMINE-SUBSTITUTED QUINOLONES USEFUL AS INDUCIBLE NITRIC OXIDE SYNTHASE INHIBITORS

Novel diarylamine-substituted quinolone compounds and pharmaceutical compositions, certain of which have been found to inhibit inducible NOS synthase have been discovered, together with methods of synthesizing and using the compounds including methods for the treatment of iNOS-mediated diseases in a patient by administering the compounds.

First direct C-2-lithiation of 4-DMAP. Convenient access to reactive functional derivatives and ligands

The first direct α-lithiation of 4-DMAP has been peformed via reaction with the BuLi-Me2N(CH2)2-OLi (BuLi-LiDMAE) reagent. This new methodology avoids the use of a activation-lithiation-regeneration sequence or halogen-met