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528315

Sigma-Aldrich

2-Methyl-N-ethyl-N-(2-cyanoethyl)-4-aminobenzaldehyde

98%

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About This Item

Linear Formula:
(NCCH2CH2)(C2H5)NC6H3(CH3)CHO
CAS Number:
119-97-1
Molecular Weight:
216.28
EC Number:
204-362-2
MDL number:
MFCD02683509
UNSPSC Code:
12352100
PubChem Substance ID:
24877577
NACRES:
NA.22

Quality Level

100

assay

98%

mp

64-67 °C (lit.)

functional group

aldehyde
amine
nitrile

storage temp.

2-8°C

SMILES string

CCN(CCC#N)c1ccc(C=O)c(C)c1

InChI

1S/C13H16N2O/c1-3-15(8-4-7-14)13-6-5-12(10-16)11(2)9-13/h5-6,9-10H,3-4,8H2,1-2H3

InChI key

VTXVKMVZEXXUIC-UHFFFAOYSA-N

Related Categories

Application

2-Methyl-N-ethyl-N-(2-cyanoethyl)-4-aminobenzaldehyde may be used to synthesize 2,6-bis[2-methyl-4(N-ethyl-N-ethylacetonitrile)aniline]cyclohexanone and (1E,4E)-1,5-bis[2-methyl-4(N-ethyl-Nethylacetonitrile)aniline]-1,4-pentadiene-3-one.

pictograms

Exclamation mark
GHS07

signalword

Warning

Hazard Classifications

Eye Irrit. 2 - Skin Irrit. 2 - STOT SE 3

target_organs

Respiratory system

Storage Class

11 - Combustible Solids

wgk_germany

WGK 3

flash_point_f

Not applicable

flash_point_c

Not applicable

ppe

dust mask type N95 (US), Eyeshields, Gloves

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Certificates of Analysis (COA)

Lot/Batch Number
03623CI
D00110401
D00090892
D00050029
D00047241

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Waqas Ahmad et al.
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Arachidonic acid and its metabolites have generated a heightened interest due to their significant role in inflammation. Inhibiting the enzymes involved in arachidonic acid metabolism has been considered as the synergistic anti-inflammatory effect. A series of novel curcumin diarylpentanoid analogues

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