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Merck
CN

392650

2,2,5,5-Tetramethyl-3-pyrroline-3-carboxamide

99%

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About This Item

Empirical Formula (Hill Notation):
C9H16N2O
CAS Number:
Molecular Weight:
168.24
UNSPSC Code:
12352100
NACRES:
NA.22
PubChem Substance ID:
EC Number:
243-331-8
MDL number:
Assay:
99%
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Quality Level

assay

99%

mp

180-182 °C (lit.)

functional group

amide

SMILES string

CC1(C)NC(C)(C)C(=C1)C(N)=O

InChI

1S/C9H16N2O/c1-8(2)5-6(7(10)12)9(3,4)11-8/h5,11H,1-4H3,(H2,10,12)

InChI key

ACFYUJLIWIDSFM-UHFFFAOYSA-N

General description

2,2,5,5-Tetramethyl-3-pyrroline-3-carboxamide is a carboxamide of a hydrogenated pyrrole derivative. It is a sterically hindered amino compound having amino alkyl side chain. The antiarrhythmic activity of some of the derivatives of 2,2,5,5-tetramethyl-3-pyrroline-3-carboxamide have been evaluated.

Application

2,2,5,5-Tetramethyl-3-pyrroline-3-carboxamide may be used in the synthesis of 2,2,5,5-tetramethyl-3-pyrrolidinecarboxamide and 3-carbamoyl-2,2,5,5-tetramethyl-3-pyrrolin-1-yloxy free radical.


pictograms

Exclamation mark

signalword

Warning

Hazard Classifications

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

target_organs

Respiratory system

Storage Class

11 - Combustible Solids

wgk

WGK 3

flash_point_f

Not applicable

flash_point_c

Not applicable

ppe

dust mask type N95 (US), Eyeshields, Gloves



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Ampika Phutim-Mangkhalthon et al.
Photodiagnosis and photodynamic therapy, 31, 101747-101747 (2020-03-23)
Photodynamic therapy improves oral mucositis treatment. The reactive oxygen species (ROS) generated from this reaction could contribute to an anti-inflammatory effect by suppressing inflammatory cells. To evaluate the anti-inflammatory effect of photodynamic therapy using guaiazulene and a red laser in
Rei Miyano et al.
Journal of bioscience and bioengineering, 129(4), 508-513 (2019-12-16)
A new nitrogen-containing compound, trichothioneic acid, was discovered from the metabolites of fungal strain FKI-7573 using a mass spectrometry screening method guided by odd number of molecular weights, which indicates compounds that contain an odd number of nitrogen atoms. Strain
O H Hankovszky et al.
Journal of medicinal chemistry, 29(7), 1138-1152 (1986-07-01)
N-(omega-Aminoalkyl)-2,2,5,5-tetramethyl-3-pyrroline- or -pyrrolidine-3-carboxamides were acylated on the primary amino group of the side chain by means of reactive acid derivatives (acid chlorides, activated esters, phthalic anhydrides, phthalimide, 2-alkyl-4H-3,1-benzoxazin-4-ones) or they were alkylated by forming the Schiff bases and subsequent sodium



Global Trade Item Number

SKUGTIN
392650-5G04061833322789