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94692-05-4

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94692-05-4 Usage

General Description

Ethyl 1-phenyl-5-(1H-pyrrol-1-yl)-1H-pyrazole-4-carboxylate is a chemical compound with the molecular formula C19H17N3O2. It is a pyrazole derivative that contains both an ethyl ester and a phenyl group, as well as a pyrrole ring. ETHYL 1-PHENYL-5-(1H-PYRROL-1-YL)-1H-PYRAZOLE-4-CARBOXYLATE has potential applications in the fields of pharmaceuticals and organic synthesis, and it may have biological activities that make it of interest for further study. The specific properties and potential uses of ethyl 1-phenyl-5-(1H-pyrrol-1-yl)-1H-pyrazole-4-carboxylate would depend on its synthesis and any subsequent research and testing that has been conducted.

Check Digit Verification of cas no

The CAS Registry Mumber 94692-05-4 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 9,4,6,9 and 2 respectively; the second part has 2 digits, 0 and 5 respectively.
Calculate Digit Verification of CAS Registry Number 94692-05:
(7*9)+(6*4)+(5*6)+(4*9)+(3*2)+(2*0)+(1*5)=164
164 % 10 = 4
So 94692-05-4 is a valid CAS Registry Number.
InChI:InChI=1/C16H15N3O2/c1-2-21-16(20)14-12-17-19(13-8-4-3-5-9-13)15(14)18-10-6-7-11-18/h3-12H,2H2,1H3

94692-05-4SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 16, 2017

Revision Date: Aug 16, 2017

1.Identification

1.1 GHS Product identifier

Product name ethyl 1-phenyl-5-pyrrol-1-ylpyrazole-4-carboxylate

1.2 Other means of identification

Product number -
Other names HMS2324M14

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:94692-05-4 SDS

94692-05-4Relevant articles and documents

Synthesis, reactions and antimicrobial activity of some new 1,3,4-oxadiazoles, 1,2,4-triazoles and 1,3,4-thiadiazines derived from pyrazole

Farghaly,Vanelle,El-Kashef

, p. 255 - 262 (2007/10/03)

New 1,3,4-oxadiazoles, 1,2,4-triazoles and 1,3,4-thiadiazines containing a pyrazolyl moiety 7-14 were prepared using ethyl 5-amino-1-phenyl-1H-pyrazole-3- carboxylate 1 as a starting material. The newly synthesized compounds were screened for their in vitro anti-bacterial and anti-fungal activity.

Non-steroidal antiinflammatory agents. V. Synthesis of 1-aryl-5-(l-pyrryl)-pyrazolyl-4-acetic acids with potential antiinflammatory activity

Corelli,Massa,Stefancich,Silvestri,Artico,Pantaleoni,Palumbo,Fanini,Giorgi

, p. 251 - 265 (2007/10/02)

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NEW CONDENSED TRI- AND TETRACYCLIC PYRAZOLE RING SYSTEMS

Svetlik, Jan

, p. 2513 - 2516 (2007/10/02)

1-Phenylpyrrazolopyrrolopyrazine and its 5-aza analogue were synthesized from ethyl 5-amino-1-phenylpyrazole-4-carboxylate.Additional azolo ring annelations on the pyrazine part of the first heterocycle afforded new tetracyclic systems with two common nitrogen atoms.

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