1H-Benzotriazole-1-methanol

• Catalog No.: 410233
• CAS Number: 28539-02-8
• M. F.: C7H7N3O
• M. W.: 149.14998
• Purity: 98%

SYNONYMS

• Title: 1H-苯并三唑-1-甲醇
• IUPAC name: 1H-1,2,3-benzotriazol-1-ylmethanol
• IUPAC Traditional name: 1,2,3-benzotriazol-1-ylmethanol
• Synonyms: 1-(Hydroxymethyl)benzotriazole; 1-Benzotriazolemethanol; NSC 12463

DATABASE IDS

• PubChem SID: 24865702
• MDL Number: MFCD00179118
• CAS Number: 28539-02-8

PROPERTIES

• Empirical Formula (Hill Notation): C7H7N3O
• Purity: 98%
• Melting Point: 150-152 °C(lit.)
• GHS Signal Word: Warning
• GHS Hazard statements: H315-H319-H335
• European Hazard Symbols: Irritant (Xi)
• Personal Protective Equipment: dust mask type N95 (US), Eyeshields, Gloves
• GHS Precautionary statements: P261-P305 + P351 + P338
• Risk Statements: 36/37/38
• Safety Statements: 26-36
• German water hazard class: 3

DETAILS

Description (English)

Application
Safe reagent for the in situ generation of anhydrous formaldehyde in organic solvents.8
Catalyst for:
• Hydrolysis of phenyl esters of a-furoic acid1Used as:
• Corrosion inhibitor of iron in aerated acidic media2
• Reactive oxygen scavenger3Reactant for:
• Synthesis of hydroxy-skipped bis-homo-inositols as potential glycosidase inhibitors via Sharpless asymmetric dihydroxylation and substrate-directed anionic hydroxymethylation4
• Enantioselective synthesis of aplysin utilizing a palladium-catalyzed addition of an arylboronic acid to an allenic alcohol, followed by Eschenmoser/Claisen rearrangement5
• Synthesis of substituted dihydroquinoline carboxylic acids as antitumor and HIV-1 integrase inhibitors6
• Gosteli-Claisen rearrangement7
Packaging
10, 50 g in glass bottle

Description (简体中文)

Application
用于在有机溶剂中原位合成无水甲醛的安全剂。8
Catalyst for:
• Hydrolysis of phenyl esters of a-furoic acid1Used as:
• Corrosion inhibitor of iron in aerated acidic media2
• Reactive oxygen scavenger3Reactant for:
• Synthesis of hydroxy-skipped bis-homo-inositols as potential glycosidase inhibitors via Sharpless asymmetric dihydroxylation and substrate-directed anionic hydroxymethylation4
• Enantioselective synthesis of aplysin utilizing a palladium-catalyzed addition of an arylboronic acid to an allenic alcohol, followed by Eschenmoser/Claisen rearrangement5
• Synthesis of substituted dihydroquinoline carboxylic acids as antitumor and HIV-1 integrase inhibitors6
• Gosteli-Claisen rearrangement7
包装
10, 50 g in glass bottle