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3-Pyrazolecarboxylic acid, 4-amino-5-(p-chlorophenyl)-, ethyl ester is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

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  • 91857-59-9 Structure
  • Basic information

    1. Product Name: 3-Pyrazolecarboxylic acid, 4-amino-5-(p-chlorophenyl)-, ethyl ester
    2. Synonyms:
    3. CAS NO:91857-59-9
    4. Molecular Formula:
    5. Molecular Weight: 265.699
    6. EINECS: N/A
    7. Product Categories: N/A
    8. Mol File: 91857-59-9.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: 3-Pyrazolecarboxylic acid, 4-amino-5-(p-chlorophenyl)-, ethyl ester(CAS DataBase Reference)
    10. NIST Chemistry Reference: 3-Pyrazolecarboxylic acid, 4-amino-5-(p-chlorophenyl)-, ethyl ester(91857-59-9)
    11. EPA Substance Registry System: 3-Pyrazolecarboxylic acid, 4-amino-5-(p-chlorophenyl)-, ethyl ester(91857-59-9)
  • 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: 91857-59-9(Hazardous Substances Data)

91857-59-9 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 91857-59-9 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 9,1,8,5 and 7 respectively; the second part has 2 digits, 5 and 9 respectively.
Calculate Digit Verification of CAS Registry Number 91857-59:
(7*9)+(6*1)+(5*8)+(4*5)+(3*7)+(2*5)+(1*9)=169
169 % 10 = 9
So 91857-59-9 is a valid CAS Registry Number.

91857-59-9Relevant articles and documents

Synthesis of new series of pyrazolo[4,3-d]pyrimidin-7-ones and pyrido[2,3-d]pyrimidin-4-ones for their bacterial and cyclin-dependent kinases (CDKs) inhibitory activities

Geffken, Detlef,Soliman, Raafat,Soliman, Farid S.D.,Abdel-Khalek, Magdi M.,Issa, Doaa A.E.

, p. 408 - 420 (2012/04/04)

Two series of pyrazolo[4,3-d]pyrimidin-7-ones and pyrido[2,3-d]pyrimidin-4- ones were designed, synthesised, and evaluated for their antibacterial activities and CDKs inhibitory activities. The pyridazine derivative: 6-phenyl-5-phenylhydrazono-2,3,4,5-tetrahydropyridazine- 3,4-dione (3a) revealed activity against Staphylococcus aureus as Gram-positive bacteria while compound 2-(2- Ethoxyphenyl-5-Phenylpiperazinosulfonamido)-3H-pyrido [2,3-d]pyrimidin-4-one (13c) was showing moderate antifungal activity against Candida albicans.

Novel 6-N-arylcarboxamidopyrazolo[4,3-d]pyrimidin-7-one derivatives as potential anti-cancer agents

Devegowda, Vani N.,Kim, Jung Hyun,Han, Ki-Cheol,Yang, Eun Gyeong,Choo, Hyunah,Pae, Ae Nim,Nam, Ghilsoo,Choi, Kyung Il

scheme or table, p. 1630 - 1633 (2010/06/19)

A novel series of 3,5,6-trisubstituted pyrazolo[4,3-d]pyrimidin-7-one derivatives, especially 6-N-arylcarboxamidopyrazolo[4,3-d]pyrimidin-7-ones were synthesized and evaluated for their in vitro anticancer activities against various human cancer cell line

Synthesis of novel pyrazolopyrrolizinones as prospective anticancer agents

Rochais, Christophe,Sopkova-de Oliveira Santos, Jana,Dallemagne, Patrick,Rault, Sylvain

, p. 2063 - 2077 (2008/01/27)

Herein we describe the access of novel pyrazolopyrrolizinones from commercial arylacetonitriles. The first step conducts to the corresponding aminoester which was first submitted to Clauson-Kaas procedure. Amidification and cyclisation afford then the fir

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