Skip to Content
MilliporeSigma

163821

3-Methoxy-2-nitrobenzaldehyde

≥97%

Slide 1 of 1
Sign In to View Organizational & Contract Pricing

Select a Size

5 G

$334.00

25 G

$608.25

$334.00

Available to ship TODAYDetails

Request a Bulk Order
Ships Every 4 weeks

About This Item

Linear Formula:
CH3OC6H3(NO2)CHO
CAS Number:
53055-05-3
Molecular Weight:
181.15
Beilstein/REAXYS Number:
1959385
EC Number:
258-332-9
MDL number:
MFCD00007135
UNSPSC Code:
12352100
PubChem Substance ID:
24850038
NACRES:
NA.22

Key Documents

View All Documentation

Skip To

Technical Service
Need help? Our team of experienced scientists is here for you.
Let Us Assist

Quality Level

100

assay

≥97%

form

solid

mp

97-101 °C (lit.)

functional group

aldehyde
nitro

SMILES string

[H]C(=O)c1cccc(OC)c1[N+]([O-])=O

InChI

1S/C8H7NO4/c1-13-7-4-2-3-6(5-10)8(7)9(11)12/h2-5H,1H3

InChI key

GDTUACILWWLIJF-UHFFFAOYSA-N

Looking for similar products? Visit Product Comparison Guide

Related Categories

Compare Similar Items

View Full Comparison

Show Differences

1 of 4

This Item
144320139033122068
3-Methoxy-2-nitrobenzaldehyde ≥97%

Sigma-Aldrich

163821

3-Methoxy-2-nitrobenzaldehyde

4-Hydroxy-3-nitrobenzaldehyde 97%

Sigma-Aldrich

144320

4-Hydroxy-3-nitrobenzaldehyde

2-Chloro-5-nitrobenzaldehyde 97%

Sigma-Aldrich

139033

2-Chloro-5-nitrobenzaldehyde

trans-4-Methoxy-3-buten-2-one technical grade, 90%

Sigma-Aldrich

122068

trans-4-Methoxy-3-buten-2-one

assay

≥97%

assay

97%

assay

97%

assay

90%

Quality Level

100

Quality Level

100

Quality Level

100

Quality Level

100

form

solid

form

-

form

-

form

-

mp

97-101 °C (lit.)

mp

140-142 °C (lit.)

mp

75-77 °C (lit.)

mp

-

functional group

aldehyde

functional group

aldehyde, nitro

functional group

aldehyde, chloro, nitro

functional group

ether, ketone

General description

3-Methoxy-2-nitrobenzaldehyde undergoes 1,4-diazabicyclo[2.2.2]octane-catalyzed reaction with methyl vinyl ketone (MVK) to afford normal Baylis-Hillman adduct, the MVK dimer and a pair of diastereomeric bis-(MVK)Baylis-Hillman adducts[1].

Application

3-Methoxy-2-nitrobenzaldehyde was used in the synthesis of 8-hydroxyquinazoline, methy-3-methoxyanthranilate and 3-methoxy-2-nitrobenzylidenebisformamide[2].

Storage Class

11 - Combustible Solids

wgk_germany

WGK 3

flash_point_f

Not applicable

flash_point_c

Not applicable

ppe

Eyeshields, Gloves, type N95 (US)

Choose from one of the most recent versions:

Certificates of Analysis (COA)

Lot/Batch Number
MKCW8160
MKBD4438V
MKBD4438
08423KH
03908TD

Don't see the Right Version?

If you require a particular version, you can look up a specific certificate by the Lot or Batch number.

Search for a COA

Already Own This Product?

Find documentation for the products that you have recently purchased in the Document Library.

Visit the Document Library

972. Analogues of 8-hydroxyquinoline having additional cyclic nitrogen atoms. Part I. Preparative.
Albert A and Hampton A.
Journal of the Chemical Society, 4985-4993 (1952)
Elucidation of the complex Baylis-Hillman reaction of 3-methoxy-2-nitrobenzaldehyde with methyl vinyl ketone.
Idahosa KC, et al.
South African Journal of Chemistry, 64, 144-150 (2011)

Questions

Reviews

No rating value

Active Filters

Our team of scientists has experience in all areas of research including Life Science, Material Science, Chemical Synthesis, Chromatography, Analytical and many others.

Contact Technical Service