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Merck
CN

209392

3-Methoxyphenylacetonitrile

99%

Synonym(s):

3-Methoxybenzyl cyanide

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About This Item

Linear Formula:
CH3OC6H4CH2CN
CAS Number:
19924-43-7
Molecular Weight:
147.17
UNSPSC Code:
12352100
NACRES:
NA.22
PubChem Substance ID:
24852567
EC Number:
243-428-5
Beilstein/REAXYS Number:
1865539
MDL number:
MFCD00001910
Assay:
99%
Form:
liquid

Key Documents

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InChI key

LXKNAUOWEJWGTE-UHFFFAOYSA-N

InChI

1S/C9H9NO/c1-11-9-4-2-3-8(7-9)5-6-10/h2-4,7H,5H2,1H3

SMILES string

COc1cccc(CC#N)c1

assay

99%

form

liquid

Quality Level

100

bp

164-165 °C/20 mmHg (lit.)

density

1.054 g/mL at 25 °C (lit.)

functional group

nitrile

Related Categories

Application

3-Methoxyphenylacetonitrile was used in the synthesis of:
  • new immunogen for homovanillic acid
  • β,β′-cyclobisalkylated melatoninergic phenylalkylamides
  • α-sec-butyl-3-methoxy phenylacetonitrile, antispasmodic agent

Storage Class

10 - Combustible liquids

wgk

WGK 3

flash_point_f

208.4 °F - closed cup

flash_point_c

98 °C - closed cup

ppe

Eyeshields, Gloves, type ABEK (EN14387) respirator filter

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Certificates of Analysis (COA)

Lot/Batch Number
0000519101
0000519101
0000351882
0000351882
0000124573

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An Efficient Synthesis of Simple, ?,?′-Cyclobisalkylated Melatoninergic Phenylalkylamides.
Tsotinis A, et al.
Letters in Organic Chemistry, 4(2), 92-95 (2007)
Synthesis of a homovanillic acid immunogen that incorporates an isosteric group designed to generate antibodies with improved specificity.
Gallacher G, et al.
Biogenic Amines, 11(1), 49-62 (1995)
Suphannika Intanon et al.
Journal of agricultural and food chemistry, 62(30), 7423-7429 (2014-07-08)
Meadowfoam (Limnanthes alba Hartw. ex Benth.) is an oilseed crop grown in the Willamette Valley of Oregon. Meadowfoam seed meal (MSM), a byproduct after oil extraction, contains 2-4% glucosinolate (glucolimnanthin). Activated MSM, produced by adding freshly ground myrosinase-active meadowfoam seeds
Antispasmodic agents. 1. Syntheses and pharmacological activity of aminoalkyl 3-substituted phenylacetates.
T Kametani et al.
Journal of medicinal chemistry, 14(1), 72-75 (1971-01-01)

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