Boron tribromide solution

• Catalog No.: 15692
• CAS Number: 10294-33-4
• M. F.: BBr3
• M. W.: 250.523

SYNONYMS

• Title: 三溴化硼 溶液
• IUPAC name: tribromoborane
• IUPAC Traditional name: boron tribromide
• Synonyms: Tribromoboron

DATABASE IDS

• CAS Number: 10294-33-4
• MDL Number: MFCD00011312

PROPERTIES

• Concentration: ~1 M in methylene chloride
• Empirical Formula (Hill Notation): BBr3
• Grade: purum
• Density: 1.46 g/mL at 20 °C
• GHS Signal Word: Danger
• GHS Hazard statements: H314-H351
• European Hazard Symbols: Highly toxic (T+)
• Personal Protective Equipment: Faceshields, full-face respirator (US), Gloves, Goggles, multi-purpose combination respirator cartridge (US), type ABEK (EN14387) respirator filter
• GHS Precautionary statements: P280-P305 + P351 + P338-P310
• RID/ADR: UN 3390 6.1/PG 1
• Risk Statements: 14-26/28-35-40
• Safety Statements: 26-28-36/37/39-45
• Supplemental Hazard Statements: Reacts violently with water.
• Hazard Class: 6.1
• UN Number: 3390
• Packing Group: 1
• German water hazard class: 3

DETAILS

Description (English)

Application
Reactant for preparation of:
• Drug intermediate 6-nitro-L-DOPA1
• Luminescent polystyrene derivatives with sterically protected carbazolylborane moieties2
• High-quality boron-doped graphene via Wurtz-type reductive coupling reaction3
• Mercapto-(+)-methamphetamine haptens for synthesis of (+)-methamphetamine conjugate vaccines with improved epitope densities4
• Micrometer-sized organic molecule-DNA hybrid structures5
• Borane complexes via electrophilic aromatic borylation reactions6
• A 5-HT2C receptor agonist7
• Biphenyl-derivatives possessing tertiary amino groups as β-secretase(BACE1) inhibitors for the treatment of Alzheimer′s disease8
• A highly near-IR region fluorescent p-extended boron aza-dipyrromethene moiety unit9
• Tetrahydroisoquinoline derivatives via intramolecular cyclization of methoxy-substituted N-phenethylimides10

Description (简体中文)

Application
Reactant for preparation of:
• Drug intermediate 6-nitro-L-DOPA1
• Luminescent polystyrene derivatives with sterically protected carbazolylborane moieties2
• High-quality boron-doped graphene via Wurtz-type reductive coupling reaction3
• Mercapto-(+)-methamphetamine haptens for synthesis of (+)-methamphetamine conjugate vaccines with improved epitope densities4
• Micrometer-sized organic molecule-DNA hybrid structures5
• Borane complexes via electrophilic aromatic borylation reactions6
• A 5-HT2C receptor agonist7
• Biphenyl-derivatives possessing tertiary amino groups as β-secretase(BACE1) inhibitors for the treatment of Alzheimer′s disease8
• A highly near-IR region fluorescent p-extended boron aza-dipyrromethene moiety unit9
• Tetrahydroisoquinoline derivatives via intramolecular cyclization of methoxy-substituted N-phenethylimides10