Deoxo-Fluor® solution

• Catalog No.: 94324
• CAS Number: 202289-38-1
• M. F.: C6H14F3NO2S
• M. W.: 221.2410696

SYNONYMS

• Title: Deoxo-Fluor® 溶液
• IUPAC name: bis(2-methoxyethyl)(trifluoro-λ^4-sulfanyl)amine
• IUPAC Traditional name: bis(2-methoxyethyl)(trifluoro-λ^4-sulfanyl)amine
• Synonyms: 双(2-甲氧基乙基)氨基三氟化硫 溶液; Bis(2-methoxyethyl)aminosulfur trifluoride solution

DATABASE IDS

• CAS Number: 202289-38-1
• PubChem SID: 24889983
• MDL Number: MFCD01321415

PROPERTIES

• Concentration: ~50% in toluene (NMR)
• Empirical Formula (Hill Notation): C6H14F3NO2S
• Apperance: clear yellow liquid
• Flash Point: <10 °C
• Flash Point: <50 °F
• GHS Signal Word: Danger
• GHS Hazard statements: H225-H261-H301 + H331-H304-H314-H336-H361d-H373
• European Hazard Symbols: Flammable (F)
• European Hazard Symbols: 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: P210-P231 + P232-P261-P280-P301 + P310-P422
• RID/ADR: UN 3286 3/PG 2
• Risk Statements: 63-11-14-23/25-29-35-48/20-65
• Safety Statements: 16-26-36/37/39-45-62
• Storage Temperature: 2-8°C
• Supplemental Hazard Statements: Contact with water liberates toxic gas., Reacts violently with water.
• Hazard Class: 3
• UN Number: 3286
• Packing Group: 2
• German water hazard class: 3

DETAILS

Description (English)

Other Notes
Fluorinating agent with high thermal stability 7,8,9,10
Application
Reactant for:
• Fluorination reactions1
• Preparation of fluorinated catechols via Umpolung based nucleophilic deoxyfluorination2
• Preparation of imidazole derivatives as CXCR3 antagonists3
• Ring expansion reactions4
• Synthesis of acyl azides from carboxylic acids5
• Aldehydes or ketones from carboxylic acids and Grignard reagents via in situ generation of Weinreb amides6
Legal Information
Deoxo-Fluor is a registered trademark of Air Products & Chemicals, Inc.

Description (简体中文)

Other Notes
具有高热稳定性的氟化剂7,8,9,10
Application
Reactant for:
• Fluorination reactions1
• Preparation of fluorinated catechols via Umpolung based nucleophilic deoxyfluorination2
• Preparation of imidazole derivatives as CXCR3 antagonists3
• Ring expansion reactions4
• Synthesis of acyl azides from carboxylic acids5
• Aldehydes or ketones from carboxylic acids and Grignard reagents via in situ generation of Weinreb amides6
法律信息
Deoxo-Fluor 注册商标 Air Products & Chemicals, Inc.