60061-63-4

Basic information

• Product Name: 4-BROMO-3-(TERT-BUTYL)-1H-PYRAZOLE
• Synonyms: 4-BROMO-3-(TERT-BUTYL)-1H-PYRAZOLE;4-Bromo-5-tert-butyl-1H-pyrazole;4-bromo-3-tert-butyl-1H-pyrazole(SALTDATA: FREE);4-bromo-3-tert-butyl-2H-pyrazole
• CAS NO: 60061-63-4
• Molecular Formula: C7H11BrN2
• Molecular Weight: 203.08
• Mol File: 60061-63-4.mol
• Article Data: 3

Chemical Properties

• Appearance: /
• CAS DataBase Reference: 4-BROMO-3-(TERT-BUTYL)-1H-PYRAZOLE(CAS DataBase Reference)
• NIST Chemistry Reference: 4-BROMO-3-(TERT-BUTYL)-1H-PYRAZOLE(60061-63-4)
• EPA Substance Registry System: 4-BROMO-3-(TERT-BUTYL)-1H-PYRAZOLE(60061-63-4)

Safety Data

• Hazard Codes: Xn
• Statements: 22
• WGK Germany: 3
• Hazardous Substances Data: 60061-63-4(Hazardous Substances Data)

Usage

General Description

4-Bromo-3-(tert-butyl)-1H-pyrazole is a chemical compound with the molecular formula C7H10BrN2. It is a pyrazole derivative that is commonly used as a building block in the synthesis of pharmaceuticals and agrochemicals. It is a solid at room temperature and is typically handled as a white crystalline powder. 4-BROMO-3-(TERT-BUTYL)-1H-PYRAZOLE is known for its ability to act as a versatile intermediate in the production of various biologically active compounds. It is important to handle and store this chemical with care, as it may pose health and environmental hazards if not managed properly. Overall, 4-bromo-3-(tert-butyl)-1H-pyrazole is a valuable chemical compound with applications in the development of new drugs and agricultural products.

Upstream product

• 15802-80-9 3-tert-butyl-1H-pyrazole 

Relevant articles and documents

Substituent effects on the supramolecular aggregation of Ag I-pyrazolato trimers

The interplay of argentophilic and dipolar (π-acid...base) interactions, on one hand, and the presence or absence of interstitial solvent molecules, on the other, determines the supramolecular organization of trinuclear silver-pyrazolato complexes in the solid state. The crystal structures of one gold and six silver metallacyclic complexes of the type [MI(μ-pz*)]3, where pz* are the substituted pyrazolato anions 3,5-Ph2-pz, 3-Me-5-Ph-pz, 4-Br-3,5-Ph 2-pz, 4-Br-3-tBu-pz and 3-(o-Cl-C6H 4)-pz and M = Ag and Au, are discussed in the context of their supramolecular organization. Two silver complexes, for which the π-acid character of their Ag3-faces is maximized by their peripheral electron-withdrawing substituents, show crystal packing dominated by short Ag3...Br contacts, the first structural manifestation of supramolecular structure via dipolar interactions involving the tunable π-acidity of the Ag3-face.

Alkyl and haloalkylpyrazoles, compositions and process

Compounds of the formula: SPC1 Wherein R1 and R2 are the same or different and are hydrogen, alkyl of from 1 to 6 carbon atoms, inclusive, or phenyl; R3 is hydrogen, alkyl of from 1 to 8 carbon atoms, inclusive, phenyl, or