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Ethyl 5-benzoylamino-1-methyl-1H-pyrazole-4-carboxylate is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

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  • 99347-01-0 Structure
  • Basic information

    1. Product Name: Ethyl 5-benzoylamino-1-methyl-1H-pyrazole-4-carboxylate
    2. Synonyms: Ethyl 5-benzoylamino-1-methyl-1H-pyrazole-4-carboxylate
    3. CAS NO:99347-01-0
    4. Molecular Formula:
    5. Molecular Weight: 273.291
    6. EINECS: N/A
    7. Product Categories: N/A
    8. Mol File: 99347-01-0.mol
  • Chemical Properties

    1. Melting Point: N/A
    2. Boiling Point: N/A
    3. Flash Point: N/A
    4. Appearance: N/A
    5. Density: N/A
    6. Refractive Index: N/A
    7. Storage Temp.: N/A
    8. Solubility: N/A
    9. CAS DataBase Reference: Ethyl 5-benzoylamino-1-methyl-1H-pyrazole-4-carboxylate(CAS DataBase Reference)
    10. NIST Chemistry Reference: Ethyl 5-benzoylamino-1-methyl-1H-pyrazole-4-carboxylate(99347-01-0)
    11. EPA Substance Registry System: Ethyl 5-benzoylamino-1-methyl-1H-pyrazole-4-carboxylate(99347-01-0)
  • Safety Data

    1. Hazard Codes: N/A
    2. Statements: N/A
    3. Safety Statements: N/A
    4. WGK Germany:
    5. RTECS:
    6. HazardClass: N/A
    7. PackingGroup: N/A
    8. Hazardous Substances Data: 99347-01-0(Hazardous Substances Data)

99347-01-0 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 99347-01-0 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 9,9,3,4 and 7 respectively; the second part has 2 digits, 0 and 1 respectively.
Calculate Digit Verification of CAS Registry Number 99347-01:
(7*9)+(6*9)+(5*3)+(4*4)+(3*7)+(2*0)+(1*1)=170
170 % 10 = 0
So 99347-01-0 is a valid CAS Registry Number.

99347-01-0Relevant articles and documents

Synthesis, structural properties, and pharmacological evaluation of 2-(acylamino)thiophene-3-carboxamides and analogues thereof

Mugnaini, Claudia,Pedani, Valentina,Giunta, Daniela,Sechi, Barbara,Solinas, Maurizio,Casti, Alberto,Castelli, Maria Paola,Giorgi, Gianluca,Corelli, Federico

, p. 1782 - 1793 (2014/01/06)

We have previously reported the synthesis and the pharmacological characterization of a family of methyl 2-(acylamino)thiophene-3-carboxylates as GABAB positive allosteric modulators active both in vitro and in vivo. In the present work, we des

STUDIES ON THE SYNTHESIS OF HETEROCYCLIC COMPOUNDS. PART XII. PYRAZOLO-1,5-BENZODIAZOCINE-4,10-DIONE. A NEW RING SYSTEM

Plescia, Salvatore,Bajardi, Maria Luisa,Daidone, Giuseppe,Roccaro, Angela

, p. 105 - 112 (2007/10/02)

Treatment of N-(1-R-4-carboxypyrazol-5-yl)-2-aminobenzamides 2b,e with thionyl chloride afforded new pyrazolo-1,3-oxazinones 3b,e.When the amide group of compounds 2b,e was blocked pyrazolo-1,5-benzodiazocine-4,10-diones 6a,d were obtained.

Heterocyclic β-Enamino Esters, 39. - Synthesis of 1H-Pyrazolopyrimidines

Wamhoff, Heinrich,Ertas, Muemtaz,Atta, Sanaa M. S.

, p. 1910 - 1916 (2007/10/02)

Die Pyrazol-Enaminoester 1a, b und 4-Pyrazolcarbohydrazide 4a, b sind nuetzliche Ausgangsverbindungen fuer die Darstellung von 1H-Pyrazolopyrimidinen.So ergeben Orthoameisensaeure- und Orthoessigsaeure-triethylester mit 4a, b die 5-(Ethoxymethylena

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