23784-89-6

Basic information

• Product Name: 3-(ChloroMethyl)-1H-pyrazole
• Synonyms: 1H-Pyrazole, 3-(chloromethyl)-
• CAS NO: 23784-89-6
• Molecular Formula: C₄H₅ClN₂
• Molecular Weight: 116.5489
• Mol File: 23784-89-6.mol
• Article Data: 5

Chemical Properties

• Boiling Point: 274.8±15.0 °C(Predicted)
• Appearance: /
• Density: 1.314±0.06 g/cm3(Predicted)
• Storage Temp.: 2-8°C
• PKA: 13.12±0.10(Predicted)
• CAS DataBase Reference: 3-(ChloroMethyl)-1H-pyrazole(CAS DataBase Reference)
• NIST Chemistry Reference: 3-(ChloroMethyl)-1H-pyrazole(23784-89-6)
• EPA Substance Registry System: 3-(ChloroMethyl)-1H-pyrazole(23784-89-6)

Safety Data

• Hazardous Substances Data: 23784-89-6(Hazardous Substances Data)

Upstream product

• 270920-41-7 (1⁽²⁾H-pyrazol-3-yl)-methanol; hydrochloride 
• 23585-49-1 (1H-pyrazol-3-yl)methanol 
• 5932-27-4 ethyl 1H-pyrazole-3-carboxylate 

Downstream Products

• 135237-01-3 2-(1H-pyrazol-3-yl)acetonitrile 
• 676491-02-4 N-methyl-1-(1H-pyrazol-3-yl)methanamine 

Relevant articles and documents

19F PARASHIFT Probes for Magnetic Resonance Detection of H2O2 and Peroxidase Activity

Elevated levels of reactive oxygen species and peroxidase expression are often associated with inflammation and inflammatory diseases. We developed two novel Co(II) complexes that can be used to detect oxidative activity associated with inflammation using 19F magnetic resonance imaging (MRI). These agents display a large change in 19F chemical shift upon oxidation from Co(II) to Co(III), facilitating selective visualization of both species using chemical shift selective pulse sequences. This large chemical shift change is attributed to a large magnetic anisotropy in the high spin Co(II) complexes. Importantly, the differing reactivity of the two agents allows for detection of either H2O2 production and/or the activity of peroxidase enzymes, providing two useful platforms for 19F MR hot spot imaging of oxidative events associated with biological inflammation.

HETEROCYCLIC COMPOUNDS FOR THE INHIBITION OF PASK

Disclosed herein are new heterocyclic compounds and compositions and their application as pharmaceuticals for the treatment of disease. Methods of inhibiting PAS Kinase (PASK) activity in a human or animal subject are also provided for the treatment of diseases such as diabetes mellitus.

Mass Spectrometry of Nitroazoles. 3-Ortho Effects: The loss of OH. and H2O from Methyl Substituted Nitrodiazoles

Methyl substituted nitrodiazoles which have the substituents at adjacent positions in the ring are subject to several ortho effects.Deuterium labelling of the methyl group and the mobile N-bonded hydrogen show that the loss of OH. originates from the substituents.In some cases the N-bonded hydrogen atom participates also in the loss of OH. and of H2O.