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4-Bromotetrahydropyran_Molecular_structure_CAS_25637-16-5)
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4-Bromotetrahydropyran

Catalog No. 722456 Name Sigma Aldrich
CAS Number 25637-16-5 Website http://www.sigmaaldrich.com
M. F. C5H9BrO Telephone 1-800-521-8956
M. W. 165.02836 Fax
Purity Email
Storage Chembase ID: 68129

SYNONYMS

Title
4-溴四氢吡喃
IUPAC name
4-bromooxane
IUPAC Traditional name
4-bromooxane
Synonyms
4-Bromotetrahydro-2H-pyran
4-Bromooxacyclohexane

DATABASE IDS

CAS Number 25637-16-5
MDL Number MFCD07371501

PROPERTIES

Empirical Formula (Hill Notation) C5H9BrO
Density 1.467 g/cm3 at 25 °C
Flash Point 71 °C
Flash Point 159.8 °F
Refractive Index n20/D 1.497
GHS Pictograms GHS07
GHS Signal Word Warning
GHS Hazard statements H315-H319-H335
European Hazard Symbols Irritant Irritant (Xi)
MSDS Link Download
GHS Precautionary statements P261-P305 + P351 + P338
Risk Statements 36/37/38
Safety Statements 26-36/37/39
German water hazard class 2

DETAILS

Description (English)
Packaging
500 mg in glass bottle
Application
Reactant for:
• Nickel-catalyzed alkyl-alkyl Suzuki coupling reactions with boron reagents1
• Preparation of a selective small-molecule melanocortin-4 receptor agonist with efficacy in a pilot study of sexual dysfunction in humans2
• Preparation of aliphatic hydrocarbons via nickel-catalyzed Suzuki cross-coupling with alkylboranes3
• Preparation of anthranilic acids as antibacterial agents with human serum albumin binding affinity4
• Preparation of antiatherogenic antioxidant di-tert-butyldihydrobenzofuranols via Grignard reactions with di-tert-butyl(hydroxy)benzaldehyde derivatives5
• Synthesis of gephyrotoxin via the Schmidt reaction6
Description (简体中文)
包装
500 mg in glass bottle
Application
Reactant for:
• Nickel-catalyzed alkyl-alkyl Suzuki coupling reactions with boron reagents1
• Preparation of a selective small-molecule melanocortin-4 receptor agonist with efficacy in a pilot study of sexual dysfunction in humans2
• Preparation of aliphatic hydrocarbons via nickel-catalyzed Suzuki cross-coupling with alkylboranes3
• Preparation of anthranilic acids as antibacterial agents with human serum albumin binding affinity4
• Preparation of antiatherogenic antioxidant di-tert-butyldihydrobenzofuranols via Grignard reactions with di-tert-butyl(hydroxy)benzaldehyde derivatives5
• Synthesis of gephyrotoxin via the Schmidt reaction6

REFERENCES