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555592

1-Nitro-2-naphthaldehyde

Name: 1-Nitro-2-naphthaldehyde
Brand: ALDRICH

97%

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About This Item

Linear Formula:

O₂NC₁₀H₆CHO

CAS Number:

101327-84-8

Molecular Weight:

201.18

NACRES:

NA.22

PubChem Substance ID:

24879478

UNSPSC Code:

12352100

MDL number:

MFCD03427164

Assay:

97%

Form:

solid

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Properties

Quality Level

200

assay

97%

form

solid

mp

109-110 °C (lit.)

functional group

aldehyde, nitro

SMILES string

[O-][N+](=O)c1c(C=O)ccc2ccccc12

InChI

1S/C11H7NO3/c13-7-9-6-5-8-3-1-2-4-10(8)11(9)12(14)15/h1-7H

InChI key

XQIMHJNMEFIADP-UHFFFAOYSA-N

Description

General description

On irradiation with UV light, 1-nitro-2-naphthaldehyde gets transformed into the corresponding nitroso acid.

Application

1-Nitro-2-naphthaldehyde (NAA) may be used to prepare the precursors required for the preparation of 3-acetoxy-2-methylene-3-(1-nitronaphth-2-yl)propanoate and ethyl 3-acetoxy-2-methylene-3-(1-nitronaphth-2-yl)propanoate.

Storage Class

11 - Combustible Solids

wgk

WGK 3

flash_point_f

Not applicable

flash_point_c

Not applicable

ppe

Eyeshields, Gloves, type N95 (US)

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The Baylis-Hillman acetates as a valuable source for one-pot multistep synthesis: a facile synthesis of functionalized tri-/tetracyclic frameworks containing azocine moiety.

Deevi Basavaiah et al.

Organic letters, 9(13), 2453-2456 (2007-06-01)

The Baylis-Hillman acetates have been conveniently transformed into tri-/tetracyclic heterocyclic frameworks containing an important azocine moiety via one-pot multistep protocol involving alkylation, reduction, and cyclization sequence.

Materials and systems for two photon 3-D ROM devices.

Dvornikov AS, et al.

IEEE Transactions on Components and Packaging Technologies, 20(2), 203-212 (1997)

Global Trade Item Number

SKU	GTIN
555592-1G	04061825924199
555592-5G	04061832619613