Cas 174454-35-4,N-(4,6-DIMETHYL-2-PYRIDINYL)-3-(1-PYRROLIDINYL)-2-BUTENAMIDE

174454-35-4

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Basic information

Product Name: N-(4,6-DIMETHYL-2-PYRIDINYL)-3-(1-PYRROLIDINYL)-2-BUTENAMIDE
Synonyms: N-(4,6-DIMETHYL-2-PYRIDINYL)-3-(1-PYRROLIDINYL)-2-BUTENAMIDE;(2E)-N-(4,6-dimethylpyridin-2-yl)-3-(pyrrolidin-1-yl)but-2-enamide
CAS NO:174454-35-4
Molecular Formula: C15H21N3O
Molecular Weight: 259.35
EINECS: N/A
Product Categories: N/A
Mol File: 174454-35-4.mol

Chemical Properties

Melting Point: N/A
Boiling Point: N/A
Flash Point: N/A
Appearance: /
Density: N/A
Refractive Index: N/A
Storage Temp.: N/A
Solubility: N/A
CAS DataBase Reference: N-(4,6-DIMETHYL-2-PYRIDINYL)-3-(1-PYRROLIDINYL)-2-BUTENAMIDE(CAS DataBase Reference)
NIST Chemistry Reference: N-(4,6-DIMETHYL-2-PYRIDINYL)-3-(1-PYRROLIDINYL)-2-BUTENAMIDE(174454-35-4)
EPA Substance Registry System: N-(4,6-DIMETHYL-2-PYRIDINYL)-3-(1-PYRROLIDINYL)-2-BUTENAMIDE(174454-35-4)

Safety Data

Hazard Codes: N/A
Statements: N/A
Safety Statements: N/A
WGK Germany:
RTECS:
HazardClass: N/A
PackingGroup: N/A
Hazardous Substances Data: 174454-35-4(Hazardous Substances Data)

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Check Digit Verification of cas no

The CAS Registry Mumber 174454-35-4 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,7,4,4,5 and 4 respectively; the second part has 2 digits, 3 and 5 respectively.
Calculate Digit Verification of CAS Registry Number 174454-35:
(8*1)+(7*7)+(6*4)+(5*4)+(4*5)+(3*4)+(2*3)+(1*5)=144
144 % 10 = 4
So 174454-35-4 is a valid CAS Registry Number.

174454-35-4Upstream product

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174454-36-5 N-(4,6-DIMETHYL-2-PYRIDYL)-3-(1-PYRROLIDINYL)BUTANAMIDE

174454-35-4Relevant academic research and scientific papers

Synthesis and anti-inflammatory activity of N-(4,6-dimethylpyridin-2-yl) β-ketoamides and derivatives

Robert-Piessard,Duval,Seraphin,Robert,Nourrisson,Le Baut,Grimaud

, p. 295 - 299 (2007/10/03)

A novel series of 6-amino-2,4-lutidine (6-AL) derivatives were synthesized and evaluated for anti-inflammatory activity. Starting from the pharmacophoric β-ketoamide grouping present in oxicams, we prepared the N-(4,6-dimethylpyridin-2-yl) acetoacetamide

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