1,3-Bis(2,4,6-trimethylphenyl)imidazolinium chloride

• Catalog No.: 656631
• CAS Number: 173035-10-4
• M. F.: C21H27ClN2
• M. W.: 342.90548
• Purity: 95%

SYNONYMS

• Title: 1,3-双(2,4,6-三甲基苯基)氯化咪唑
• IUPAC name: 1,3-bis(2,4,6-trimethylphenyl)-4,5-dihydro-3H-1λ^5,3-imidazol-1-ylium chloride
• IUPAC Traditional name: 1,3-bis(2,4,6-trimethylphenyl)-4,5-dihydro-1λ^5,3-imidazol-1-ylium chloride
• Synonyms: 1,3-二(2,4,6-三甲苯)咪唑氯盐; 1,3-Dimesitylimidazolidinium chloride; 4,5-Dihydro-1,3-dimesityl-1H-imidazolium chloride; 4,5-Dihydro-1,3-bis(2,4,6-trimethylphenyl)-1H-imidazolium chloride; N,N′-(2,4,6-Trimethylphenyl)dihydroimidazolium chloride

DATABASE IDS

• PubChem SID: 24884213
• MDL Number: MFCD09039279
• CAS Number: 173035-10-4

PROPERTIES

• Empirical Formula (Hill Notation): C21H27ClN2
• Purity: 95%
• Melting Point: 280-286 °C
• GHS Signal Word: Warning
• GHS Hazard statements: H315-H319-H335
• European Hazard Symbols: Irritant (Xi)
• Personal Protective Equipment: Eyeshields, full-face respirator (US), Gloves, multi-purpose combination respirator cartridge (US), type ABEK (EN14387) respirator filter
• GHS Precautionary statements: P261-P305 + P351 + P338
• Risk Statements: 36/37/38
• Safety Statements: 26-36
• German water hazard class: 3

DETAILS

Description (English)

Packaging
1, 5 g in glass bottle
Application
N-Heterocyclic Carbene Ligands Precursor to an N-heterocyclic carbene catalysts used for:
• A regioselective cycloadditon of terminal acetylenes with azides leading to 1,4-disubstitutedtriazoles. Internal acetylenes can also be used with this catalyst.1
• Markovnikov-type hydration of terminal alkynes2
• Hydrosilylation of ketones and cycloaddition of azides and alkynes3
• Suzuki-Miyaura reactions4
• Luminescence experiments5

Description (简体中文)

包装
1, 5 g in glass bottle
Application
N-Heterocyclic Carbene Ligands Precursor to an N-heterocyclic carbene catalysts used for:
• A regioselective cycloadditon of terminal acetylenes with azides leading to 1,4-disubstitutedtriazoles. Internal acetylenes can also be used with this catalyst.1
• Markovnikov-type hydration of terminal alkynes2
• Hydrosilylation of ketones and cycloaddition of azides and alkynes3
• Suzuki-Miyaura reactions4
• Luminescence experiments5