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101476-66-8

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101476-66-8 Usage

Chemical group

Pyrazole compounds

Derivative

N-ethyl-5-phenyl substituent

Physical form

Crystalline solid

Molecular weight

200.24 g/mol

Potential applications

Pharmaceutical industry (development of new drugs for various medical conditions)

Value

Valuable building block for the synthesis of other chemical compounds with potential therapeutic effects

Additional research needed

To understand its full potential and applications.

Check Digit Verification of cas no

The CAS Registry Mumber 101476-66-8 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,0,1,4,7 and 6 respectively; the second part has 2 digits, 6 and 6 respectively.
Calculate Digit Verification of CAS Registry Number 101476-66:
(8*1)+(7*0)+(6*1)+(5*4)+(4*7)+(3*6)+(2*6)+(1*6)=98
98 % 10 = 8
So 101476-66-8 is a valid CAS Registry Number.

101476-66-8SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 20, 2017

Revision Date: Aug 20, 2017

1.Identification

1.1 GHS Product identifier

Product name N-ethyl-5-phenyl-1H-pyrazol-3-amine

1.2 Other means of identification

Product number -
Other names N-ethyl-3-phenyl-1H-pyrazol-5-amine

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:101476-66-8 SDS

101476-66-8Relevant articles and documents

Synthesis of CNS potentially active bicyclic and tricyclic derivatives of pyrazolo[1,5-a][1,3]diazepines

Costanzo,Bruni,Auzzi,Selleri,Vettori

, p. 695 - 697 (2007/10/02)

-

Reaction of Polarized Keten S,N-Acetals with Hydrazine: A Facile General Route to 3(5)-Substitutedamino-4,5(3)-substitutedpyrazoles

Vishwakarma, J. N.,Chowdhury, B. K. Roy,Ila, H.,Junjappa, H.

, p. 472 - 476 (2007/10/02)

A convenient general route for 3(5)-aryl-5(3)-N-aryl/alkyl/benzyl/amino-1(H)-pyrazoles (2a-r) and 3(5)-amino-5(3)-arylamino-4-cyano/aryl-pyrazoles (5a-c) has been developed involving the reaction of respective polarized keten S,N-acetals with hydrazine hy

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