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685488

1H-Pyrrolo[2,3-f]quinoline

Name: 1<I>H</I>-Pyrrolo[2,3-<I>f</I>]quinoline
Brand: ALDRICH

97%

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About This Item

Empirical Formula (Hill Notation):

C₁₁H₈N₂

CAS Number:

233-36-3

Molecular Weight:

168.19

NACRES:

NA.22

PubChem Substance ID:

329760973

UNSPSC Code:

12352100

MDL number:

MFCD00462208

Assay:

97%

Form:

solid

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Properties

assay

97%

form

solid

mp

235-240 °C

SMILES string

c1cnc2ccc3cc[nH]c3c2c1

InChI

1S/C11H8N2/c1-2-9-10(12-6-1)4-3-8-5-7-13-11(8)9/h1-7,13H

InChI key

IVCGJOSPVGENCT-UHFFFAOYSA-N

Description

Application

Useful fused pyridino-indole for pharmaceutical research.

pictograms

GHS06,GHS05

signalword

Danger

hcodes

H301,H315,H318,H335

pcodes

P261 - P264 - P280 - P301 + P310 - P302 + P352 - P305 + P351 + P338

Hazard Classifications

Acute Tox. 3 Oral - Eye Dam. 1 - Skin Irrit. 2 - STOT SE 3

target_organs

Respiratory system

Storage Class

6.1C - Combustible acute toxic Cat.3 / toxic compounds or compounds which causing chronic effects

wgk

WGK 3

flash_point_f

Not applicable

flash_point_c

Not applicable

ppe

dust mask type N95 (US), Eyeshields, Faceshields, Gloves

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Certificates of Analysis (COA)

Lot/Batch Number

04224EH

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Microwave assisted Leimgruber-Batcho reaction for the preparation of indoles, azaindoles and pyrroylquinolines.

Jason Siu et al.

Organic & biomolecular chemistry, 2(2), 160-167 (2004-01-23)

The development of enhanced conditions for Lewis acid catalysed Leimgruber-Batcho indole synthesis using microwave acceleration is described. This approach has permitted the preparation of a variety of heteroaromatic enamine intermediates in good yield and high purities. Subsequent catalytic hydrogenation reactions

Global Trade Item Number

SKU	GTIN
685488-1G	04061832759081