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Merck
모든 사진(1)

문서

392588

Sigma-Aldrich

2,2,5,5-Tetramethyl-3-pyrrolidinecarboxamide

98%

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About This Item

실험식(Hill 표기법):
C9H18N2O
CAS Number:
Molecular Weight:
170.25
EC Number:
MDL number:
UNSPSC 코드:
12352100
PubChem Substance ID:
NACRES:
NA.22

분석

98%

형태

solid

mp

128-131 °C (lit.)

SMILES string

CC1(C)CC(C(N)=O)C(C)(C)N1

InChI

1S/C9H18N2O/c1-8(2)5-6(7(10)12)9(3,4)11-8/h6,11H,5H2,1-4H3,(H2,10,12)

InChI key

POAGFQOGFRYOFM-UHFFFAOYSA-N

일반 설명

2,2,5,5-Tetramethyl-3-pyrrolidinecarboxamide (2,2,5,5-Tetramethylpyrrolidine-3-carboxamide) is a carboxamide of hydrogenated pyrrole derivative. Its synthesis by the hydrogenation of 2,2,5,5-tetramethyl-3-pyrroline-3-carboxamide has been reported. The antiarrhythmic activity of some of the derivatives of 2,2,5,5-tetramethylpyrrolidine-3-carboxamide has been evaluated.
2,2,5,5-Tetramethyl-3-pyrrolidinecarboxamide, a pyrrolidine derivative, is a cyclic (five-membered ring) secondary amine having four carbon atoms and one nitrogen atom. Various physical properties (freezing point, boiling point, density and refractive index) of 2,2,5,5-tetramethyl-3-pyrrolidinecarboxamidehave been reported.

애플리케이션

2,2,5,5-Tetramethyl-3-pyrrolidinecarboxamide may be used in the synthesis of its nitroxide, 3-carbamoyl-2,2,5,5-tetramethyl-1-pyrrolidinyloxy free radical.

픽토그램

Exclamation mark

신호어

Warning

유해 및 위험 성명서

Hazard Classifications

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

표적 기관

Respiratory system

Storage Class Code

11 - Combustible Solids

WGK

WGK 3

Flash Point (°F)

Not applicable

Flash Point (°C)

Not applicable

개인 보호 장비

dust mask type N95 (US), Eyeshields, Gloves


시험 성적서(COA)

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문서 라이브러리 방문

Nitroxide free radicals in the hydrogenated pyrrole series.
Rozantsev EG, et al.
Russian Chemical Bulletin, 15(4), 638-641 (1966)
Yaws CL.
The Yaws Handbook of Physical Properties for Hydrocarbons and Chemicals, 260-260 (2015)
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

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