Cas 260047-13-0,N-(4-CHLOROPHENYL)-3,5-DIMETHYL-4-ISOXAZOLECARBOXAMIDE

260047-13-0

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Basic information

Product Name: N-(4-CHLOROPHENYL)-3,5-DIMETHYL-4-ISOXAZOLECARBOXAMIDE
Synonyms: N-(4-CHLOROPHENYL)-3,5-DIMETHYL-4-ISOXAZOLECARBOXAMIDE;N-(4-chlorophenyl)-3,5-dimethyl-1,2-oxazole-4-carboxamide
CAS NO:260047-13-0
Molecular Formula: C12H11ClN2O2
Molecular Weight: 250.68
EINECS: N/A
Product Categories: N/A
Mol File: 260047-13-0.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-CHLOROPHENYL)-3,5-DIMETHYL-4-ISOXAZOLECARBOXAMIDE(CAS DataBase Reference)
NIST Chemistry Reference: N-(4-CHLOROPHENYL)-3,5-DIMETHYL-4-ISOXAZOLECARBOXAMIDE(260047-13-0)
EPA Substance Registry System: N-(4-CHLOROPHENYL)-3,5-DIMETHYL-4-ISOXAZOLECARBOXAMIDE(260047-13-0)

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: 260047-13-0(Hazardous Substances Data)

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N-(4-CHLOROPHENYL)-3,5-DIMETHYL-4-ISOXAZOLECARBOXAMIDE
Cas No: 260047-13-0
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260047-13-0 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 260047-13-0 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 2,6,0,0,4 and 7 respectively; the second part has 2 digits, 1 and 3 respectively.
Calculate Digit Verification of CAS Registry Number 260047-13:
(8*2)+(7*6)+(6*0)+(5*0)+(4*4)+(3*7)+(2*1)+(1*3)=100
100 % 10 = 0
So 260047-13-0 is a valid CAS Registry Number.

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260047-13-0Relevant articles and documents

Oxidative Cyclization of β-Aminoacrylamides Mediated by PhIO: Chemoselective Synthesis of Isoxazoles and 2 H-Azirines

Li, Chaoran,Yuan, Jingwen,Zhang, Qian,Bhujanga Rao, Chitturi,Zhang, Rui,Zhao, Yanning,Deng, Bicheng,Dong, Dewen

, p. 14999 - 15008 (2018/12/14)

Cyclization of a variety of β-aminoacrylamides in the presence of iodosobenzene (PhIO) is described. This process features mild reaction conditions, simple execution, and high chemoselectivity and thereby provides an efficient protocol for the divergent s

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