3-Indoleglyoxylyl chloride

• Catalog No.: 515205
• CAS Number: 22980-09-2
• M. F.: C10H6ClNO2
• M. W.: 207.61314
• Purity: 98%

SYNONYMS

• Title: 吲哚-3-乙醛酰氯
• IUPAC name: 2-(1H-indol-3-yl)-2-oxoacetyl chloride
• IUPAC Traditional name: 2-(1H-indol-3-yl)-2-oxoacetyl chloride
• Synonyms: α-Oxoindole-3-acetyl chloride; 2-(3-Indolyl)-2-oxoacetyl chloride; NSC 128332

DATABASE IDS

• CAS Number: 22980-09-2
• PubChem SID: 24873804
• MDL Number: MFCD00015460
• EC Number: 245-362-2

PROPERTIES

• Empirical Formula (Hill Notation): C10H6ClNO2
• Purity: 98%
• Melting Point: 138 °C (dec.)(lit.)
• GHS Signal Word: Danger
• GHS Hazard statements: H314
• European Hazard Symbols: Corrosive (C)
• Personal Protective Equipment: Eyeshields, Faceshields, full-face particle respirator type N100 (US), Gloves, respirator cartridge type N100 (US), type P1 (EN143) respirator filter, type P3 (EN 143) respirator cartridges
• GHS Precautionary statements: P280-P305 + P351 + P338-P310
• RID/ADR: UN 1759 8/PG 2
• Risk Statements: 34
• Safety Statements: 26-27-36/37/39-45
• Storage Temperature: 2-8°C
• Hazard Class: 8
• UN Number: 1759
• Packing Group: 2
• German water hazard class: 3

DETAILS

Description (English)

Packaging
5 g in glass bottle
Application

• Reactant for preparation of dual IGF-1R/SRC inhibitors1
• Reactant for preparation of indolylglyoxylamides as a new class of antileishmanial agents2
• Reactant for preparation of glyoxyl analogs of indole phytoalexins as anticancer agents3
• Reactant for diastereoselective synthesis of heptacyclic core of dragmacidin E4
• Reactant for preparation of benzoylmethylpyrrolopyridinylethanedione as HIV-1 inhibitor5
• Reactant for preparation of fascaplysin-inspired diindolyls as selective inhibitors of CDK4/cyclin D16

Description (简体中文)

包装
5 g in glass bottle
Application

• Reactant for preparation of dual IGF-1R/SRC inhibitors1
• Reactant for preparation of indolylglyoxylamides as a new class of antileishmanial agents2
• Reactant for preparation of glyoxyl analogs of indole phytoalexins as anticancer agents3
• Reactant for diastereoselective synthesis of heptacyclic core of dragmacidin E4
• Reactant for preparation of benzoylmethylpyrrolopyridinylethanedione as HIV-1 inhibitor5
• Reactant for preparation of fascaplysin-inspired diindolyls as selective inhibitors of CDK4/cyclin D16