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Merck
CN

685488

Sigma-Aldrich

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

97%

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About This Item

Empirical Formula (Hill Notation):
C11H8N2
CAS Number:
233-36-3
Molecular Weight:
168.19
MDL number:
MFCD00462208
UNSPSC Code:
12352100
PubChem Substance ID:
329760973
NACRES:
NA.22

Key Documents

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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

Application

Useful fused pyridino-indole for pharmaceutical research.

Pictograms

Skull and crossbonesCorrosion
GHS06,GHS05

Signal Word

Danger

Hazard Statements

H301,H315,H318,H335

Hazard Classifications

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

Target Organs

Respiratory system

Storage Class Code

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

Personal Protective Equipment

dust mask type N95 (US), Eyeshields, Gloves

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Certificates of Analysis (COA)

Lot/Batch Number
04224EH

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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

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