36983-32-1

Basic information

• Product Name: ethyl 6-methyl-2,4-dioxoheptanoate
• Synonyms: ethyl 6-methyl-2,4-dioxoheptanoate
• CAS NO: 36983-32-1
• Molecular Formula: C₁₀H₁₆O₄
• Molecular Weight: 200.23164
• Mol File: 36983-32-1.mol
• Article Data: 10

Chemical Properties

• Appearance: /
• CAS DataBase Reference: ethyl 6-methyl-2,4-dioxoheptanoate(CAS DataBase Reference)
• NIST Chemistry Reference: ethyl 6-methyl-2,4-dioxoheptanoate(36983-32-1)
• EPA Substance Registry System: ethyl 6-methyl-2,4-dioxoheptanoate(36983-32-1)

Safety Data

• Hazardous Substances Data: 36983-32-1(Hazardous Substances Data)

Upstream product

• 64-17-5 ethanol 
• 108-10-1 4-methyl-2-pentanone 
• 95-92-1 oxalic acid diethyl ester 

Downstream Products

• 717871-79-9 1-methyl-3-isobutyl-1H-pyrazole-5-carbonyl chloride 
• 769132-77-6 1-methyl-3-isobutyl-1H-pyrazole-5-carboxylic acid 
• 133261-09-3 ethyl 1-methyl-3-isobutyl-1H-pyrazole-5-carboxylate 
• 1220348-66-2 5-isobutyl-3-(aminomethyl)-1-phenyl-1H-pyrazole 
• 1220348-60-6 5-isobutyl-1-phenyl-1H-pyrazole-3-carbaldehyde oxime 
• 926893-91-6 5-isobutyl-1-phenyl-1H-pyrazole-3-carbaldehyde 

Relevant articles and documents

Novel pyrrolidine or piperidine derivatives having activity for T-type calcium channel

A pyrrolidine or piperidine compound having activity for T - type calcium channel, wherein the pyrrolidine or piperidine compound of Formula 1 according to the present invention has an excellent antagonistic activity to, T-type calcium channel, and can be used as a preventive or therapeutic agent, for pain diseases, or cancer related to cancer, or cancer such as, epilepsy and,hepatic pain, angina. (by machine translation)

2-OXA-5-AZABICYCLO[2.2.1]HEPTAN-3-YL DERIVATIVES

The present invention relates to compounds of formula (I), wherein L is a bond, -C(O)NH-, -NHC(O)-, -CH2NHC(O)-, CH2C(O)NH-, -CH2NH-, -NH- or -NHC(O)NH-; R1 is hydrogen, lower alkyl, halogen, lower alkoxy-alkyl, lower alko

MORPHOLIN-PYRIDINE DERIVATIVES

The present invention relates to compounds of formula (I) wherein X is CR or N; R is hydrogen, halogen or lower alkyl; L is a bond, -C(O)- or -C(O)NH-; Ar is phenyl or a five or six membered heteroaryl group, containing one or two N atoms; R1 i