Boron tribromide solution

• Catalog No.: 211222
• 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

• PubChem SID: 24852661
• CAS Number: 10294-33-4
• MDL Number: MFCD00011312

PROPERTIES

• Concentration: 1.0 M in methylene chloride
• Empirical Formula (Hill Notation): BBr3
• Density: 1.467 g/mL at 25 °C
• GHS Signal Word: Danger
• GHS Hazard statements: H300-H314-H330-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: P260-P264-P280-P284-P301 + P310-P305 + P351 + P338
• 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
Used to cleave aryl methyl ethers in a synthesis of a benzopyranobenzopyran from a coumarin scaffold.11
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
Packaging
10 mL in glass bottle
2 L in Sure/Seal™
2.5 L in glass bottle
4×25, 100, 800 mL in Sure/Seal™

Description (简体中文)

Application
在由香豆素支架合成 benzopyrano benzopyran 类化合物的反应中用于裂解芳基甲基醚。11
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
包装
10 mL in glass bottle
2 L in Sure/Seal™
2.5 L in glass bottle
4×25, 100, 800 mL in Sure/Seal™