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60178-94-1

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60178-94-1 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 60178-94-1 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 6,0,1,7 and 8 respectively; the second part has 2 digits, 9 and 4 respectively.
Calculate Digit Verification of CAS Registry Number 60178-94:
(7*6)+(6*0)+(5*1)+(4*7)+(3*8)+(2*9)+(1*4)=121
121 % 10 = 1
So 60178-94-1 is a valid CAS Registry Number.

60178-94-1SDS

SAFETY DATA SHEETS

According to Globally Harmonized System of Classification and Labelling of Chemicals (GHS) - Sixth revised edition

Version: 1.0

Creation Date: Aug 17, 2017

Revision Date: Aug 17, 2017

1.Identification

1.1 GHS Product identifier

Product name ethyl 4-methyl-5-oxo-1-phenyl-4H-pyrazole-3-carboxylate

1.2 Other means of identification

Product number -
Other names 3-Aethoxycarbonyl-4-methyl-5-oxo-1-phenyl-4,5-dihydro-pyrazol

1.3 Recommended use of the chemical and restrictions on use

Identified uses For industry use only.
Uses advised against no data available

1.4 Supplier's details

1.5 Emergency phone number

Emergency phone number -
Service hours Monday to Friday, 9am-5pm (Standard time zone: UTC/GMT +8 hours).

More Details:60178-94-1 SDS

60178-94-1Downstream Products

60178-94-1Relevant articles and documents

Rhodium-Catalyzed [4+2] Annulation of N-Aryl Pyrazolones with Diazo Compounds To Access Pyrazolone-Fused Cinnolines

Lin, Chih-Yu,Huang, Wan-Wen,Huang, Ying-Ti,Dhole, Sandip,Sun, Chung-Ming

supporting information, p. 4984 - 4992 (2021/09/28)

An efficient synthesis of novel dinitrogen-fused heterocycles such as pyrazolo[1,2-a]cinnoline derivatives have been accomplished by the rhodium(III)-catalyzed reaction of N-arylpyrazol-5-ones with α-diazo compounds. This reaction proceeds through a cascade C?H activation/intramolecular cyclization with a broad substrate scope. Furthermore, this protocol is successfully extended to the unusual phosphorus-containing α-diazo compounds and cyclic diazo compounds as the cross-coupling partners to deliver the two new kinds of pyrazolo[1,2-a]cinnolinones. The control experiments were performed to reveal insight into the mechanism of this reaction, involving reversible C?H activation, migratory insertion of the diazo compound, and cascade cyclization as the key steps of the transformation. Moreover, gram-scale synthesis and further transformation of the target product demonstrate the synthetic utility of the present protocol.

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