936940-82-8

Basic information

• Product Name: CHEMBRDG-BB 4003862
• Synonyms: CHEMBRDG-BB 4003862;1-(3-Fluoro-phenyl)-1H-pyrazole-4-carbaldehyde;1-(3-fluorophenyl)-1H-pyrazole-4-carbaldehyde(SALTDATA: FREE);1H-Pyrazole-4-carboxaldehyde, 1-(3-fluorophenyl)-;1-(3-Fluorophenyl)-1H-pyrazole-4-carbaldehyde AldrichCPR;1-(3-fluorophenyl)pyrazole-4-carbaldehyde
• CAS NO: 936940-82-8
• Molecular Formula: C₁₀H₇FN₂O
• Molecular Weight: 190.17
• Product Categories: Building Blocks;Pyrazole;Chemical Synthesis;Fluorinated Building Blocks;Heterocyclic Fluorinated Building Blocks;Other Fluorinated Heterocycles;Pyrazoles
• Mol File: 936940-82-8.mol
• Article Data: 5

Chemical Properties

• Boiling Point: 241.3°C at 760 mmHg
• Flash Point: 99.7°C
• Appearance: /
• Density: 1.16g/cm³
• Vapor Pressure: 0.0561mmHg at 25°C
• Refractive Index: 1.574
• Storage Temp.: 2-8°C
• CAS DataBase Reference: CHEMBRDG-BB 4003862(CAS DataBase Reference)
• NIST Chemistry Reference: CHEMBRDG-BB 4003862(936940-82-8)
• EPA Substance Registry System: CHEMBRDG-BB 4003862(936940-82-8)

Safety Data

• WGK Germany: 3
• Hazardous Substances Data: 936940-82-8(Hazardous Substances Data)

Usage

General Description

CHEMBRDG-BB 4003862 is a chemical compound that belongs to the class of benzodiazepines, which are psychoactive drugs with sedative, hypnotic, anxiolytic, and muscle relaxant properties. It is a synthetic compound with a molecular formula of C17H13ClN2O2 and a molecular weight of 314.75 g/mol. CHEMBRDG-BB 4003862 is often used as a research tool in the study of the central nervous system and is commonly referred to as a reference standard for benzodiazepine derivatives. The exact pharmacological and toxicological properties of CHEMBRDG-BB 4003862 are not fully documented, and caution should be exercised when handling and using this chemical.

InChI:InChI=1/C9H7FN2/c10-8-3-1-4-9(7-8)12-6-2-5-11-12/h1-7H

Upstream product

• 100-97-0 hexamethylenetetramine 
• 658-27-5 m-fluorophenylhydrazine 
• 37649-86-8 1-(3-fluorophenyl)-1H-pyrazole 
• 2924-16-5 3-fluorophenylhydrazine hydrochloride 
• 76-05-1 trifluoroacetic acid 
• 462-06-6 fluorobenzene 
• 35344-95-7 1H-pyrazole-4-carbaldehyde 

Downstream Products

• 1269291-95-3 1-(3-fluorophenyl)-1H-pyrazole-4-carbonitrile 
• 138907-82-1 1-(3-fluorophenyl)-1H-pyrazole-4-carboxylic acid 

Relevant articles and documents

Electrophotocatalysis with a Trisaminocyclopropenium Radical Dication

Visible-light photocatalysis and electrocatalysis are two powerful strategies for the promotion of chemical reactions. Here, these two modalities are combined in an electrophotocatalytic oxidation platform. This chemistry employs a trisaminocyclopropenium (TAC) ion catalyst, which is electrochemically oxidized to form a cyclopropenium radical dication intermediate. The radical dication undergoes photoexcitation with visible light to produce an excited-state species with oxidizing power (3.33 V vs. SCE) sufficient to oxidize benzene and halogenated benzenes via single-electron transfer (SET), resulting in C?H/N?H coupling with azoles. A rationale for the strongly oxidizing behavior of the photoexcited species is provided, while the stability of the catalyst is rationalized by a particular conformation of the cis-2,6-dimethylpiperidine moieties.

Synthesis, docking studies, pharmacological activity and toxicity of a novel pyrazole derivative (LQFM 021) - Possible effects on phosphodiesterase

This study describes the synthetic route and molecular computational docking of LQFM 021, as well as examines its biological effects and toxicity. The docking studies revealed strong interaction of LQFM 021 to phosphodiesterase-3 (PDE-3). In isolated arte

Complete assignment of NMR data of 22 phenyl-1H-pyrazoles' derivatives

Complete assignment of 1H and 13C NMR chemical shifts and J(1H/1H and 1H/19F) coupling constants for 22 1-phenyl-1H-pyrazoles' derivates were performed using the concerted application of 1H 1D and 1H, 13C 2D gs-HSQC and gs-HMBC experiments. All 1-phenyl-1H-pyrazoles' derivatives were synthesized as described by Finar and co-workers. The formylated 1-phenyl-1H-pyrazoles' derivatives were performed under Duff's conditions. Copyright