Cas 2441-54-5,N-[3-(3,5-dimethyl-1H-pyrazol-1-yl)-3-oxo-1-phenylpropyl]-4-methylbenzenesulfonamide

2441-54-5

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Basic information

Product Name: N-[3-(3,5-dimethyl-1H-pyrazol-1-yl)-3-oxo-1-phenylpropyl]-4-methylbenzenesulfonamide
Synonyms: N-[3-(3,5-dimethyl-1H-pyrazol-1-yl)-3-oxo-1-phenylpropyl]-4-methylbenzenesulfonamide
CAS NO:2441-54-5
Molecular Formula: C₂₁H₂₃N₃O₃S
Molecular Weight: 397.49062
EINECS: N/A
Product Categories: N/A
Mol File: 2441-54-5.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-[3-(3,5-dimethyl-1H-pyrazol-1-yl)-3-oxo-1-phenylpropyl]-4-methylbenzenesulfonamide(CAS DataBase Reference)
NIST Chemistry Reference: N-[3-(3,5-dimethyl-1H-pyrazol-1-yl)-3-oxo-1-phenylpropyl]-4-methylbenzenesulfonamide(2441-54-5)
EPA Substance Registry System: N-[3-(3,5-dimethyl-1H-pyrazol-1-yl)-3-oxo-1-phenylpropyl]-4-methylbenzenesulfonamide(2441-54-5)

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: 2441-54-5(Hazardous Substances Data)

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Check Digit Verification of cas no

The CAS Registry Mumber 2441-54-5 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 2,4,4 and 1 respectively; the second part has 2 digits, 5 and 4 respectively.
Calculate Digit Verification of CAS Registry Number 2441-54:
(6*2)+(5*4)+(4*4)+(3*1)+(2*5)+(1*4)=65
65 % 10 = 5
So 2441-54-5 is a valid CAS Registry Number.

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2441-54-5Downstream Products

2441-54-5Relevant academic research and scientific papers

Synthesis of Optically Active β-Lactams by the Reaction of 2-Acyl-3-phenyl-l-menthopyrazoles with C=N Compounds

Kashima, Choji,Fukusaka, Kiyoshi,Takahashi, Katsumi

, p. 1559 - 1565 (2007/10/03)

The reaction of 1-acyl-3,5-dimethyIpyrazoles 1 with C=N compounds was kinetically controlled with syn stereoselectivity through a lithium enolate intermediate using lithium diisopropylamide. In contrast, the anti stereoselective reaction of 1 was caused b

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