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ETHYL 7-METHYLPYRAZOLO[1,5-A]PYRIMIDINE-6-CARBOXYLATE is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

90840-54-3

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90840-54-3 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 90840-54-3 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 9,0,8,4 and 0 respectively; the second part has 2 digits, 5 and 4 respectively.
Calculate Digit Verification of CAS Registry Number 90840-54:
(7*9)+(6*0)+(5*8)+(4*4)+(3*0)+(2*5)+(1*4)=133
133 % 10 = 3
So 90840-54-3 is a valid CAS Registry Number.

90840-54-3SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 15, 2017

Revision Date: Aug 15, 2017

1.Identification

1.1 GHS Product identifier

Product name Ethyl 7-methylpyrazolo[1,5-a]pyrimidine-6-carboxylate

1.2 Other means of identification

Product number -
Other names ethyl 7-methylpyrazolo<1,5-a>pyrimidin-6-carboxylate

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:90840-54-3 SDS

90840-54-3Relevant academic research and scientific papers

Novel 3,6,7-substituted pyrazolopyrimidines as positive allosteric modulators for the hydroxycarboxylic acid receptor 2 (GPR109A)

Blad, Clara C.,Van Veldhoven, Jacobus P. D.,Klopman, Corné,Wolfram, Dieter R.,Brussee, Johannes,Lane, J. Robert,Ijzerman, Adriaan P.

supporting information; experimental part, p. 3563 - 3567 (2012/06/04)

A number of pyrazolopyrimidines were synthesized and tested for their positive allosteric modulation of the HCA2 receptor (GPR109A). Compound 24, an efficacious and potent agonist and allosteric enhancer of nicotinic acid's action, was the basis for most other compounds. Interestingly, some of the compounds were found to increase the efficacy of the endogenous ligand 3-hydroxybutyrate and enhance its potency almost 10-fold. This suggests that the pyrazolopyrimidines may have therapeutic value when given alone.

Reactivity of 7-(2-Dimethylaminovinyl)pyrazolopyrimidines: Synthesis of Pyrazolopyridopyrimidine Derivatives as Potential Benzodiazepine Receptor Ligands. 2.

Bruni, Fabrizio,Selleri, Silvia,Costanzo, Annarella,Guerrini, Gabriella,Casilli, Maria Lucia,Giusti, Laura

, p. 291 - 298 (2007/10/02)

A series of pyrazolopyridopyrimidin-6-ones was obtained by reaction of ammonium acetate with ethyl 7-dimethylaminovinylpyrazolopyrimidine-6-carboxylates and these had been prepared from ethyl 7-methylpyrazolopyrimidine-6-carboxylates by reaction with dimethylformamide dimethylacetat.Under these conditions the compounds bearing a 2-hydroxy group were also O-alkylated.During the preparation of the ethyl 2-hydroxy-7-methyl-3-phenylpyrazolopyrimidine-6-carboxylate the corresponding 5-methyl isomer was isolated and identified.

Unambiguous Structure Determination of Some Pyrazolopyrimidine Derivatives by Multinuclear NMR Spectroscopy

Chimichi, Stefano,Cosimelli, Barbara,Bruni, Fabrizio,Selleri, Silvia

, p. 1117 - 1121 (2007/10/02)

The condensation of 3(5)-aminopyrazole and 5-amino-3-phenylpyrazole with ethyl 2,4-dioxopentanoate and 2-ethoxymethylidene-3-oxobutyrate has been re-investigated.Contrary to previous reports, the former reaction gives rise to both regioisomeric pyrazolo1

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