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3-bromo-7-(carboxymethyl-amino)-pyrazolo[1,5-a]pyrimidine-6-carboxylic acid 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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  • 43024-89-1 Structure
  • Basic information

    1. Product Name: 3-bromo-7-(carboxymethyl-amino)-pyrazolo[1,5-a]pyrimidine-6-carboxylic acid ethyl ester
    2. Synonyms:
    3. CAS NO:43024-89-1
    4. Molecular Formula:
    5. Molecular Weight: 343.137
    6. EINECS: N/A
    7. Product Categories: N/A
    8. Mol File: 43024-89-1.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-bromo-7-(carboxymethyl-amino)-pyrazolo[1,5-a]pyrimidine-6-carboxylic acid ethyl ester(CAS DataBase Reference)
    10. NIST Chemistry Reference: 3-bromo-7-(carboxymethyl-amino)-pyrazolo[1,5-a]pyrimidine-6-carboxylic acid ethyl ester(43024-89-1)
    11. EPA Substance Registry System: 3-bromo-7-(carboxymethyl-amino)-pyrazolo[1,5-a]pyrimidine-6-carboxylic acid ethyl ester(43024-89-1)
  • 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: 43024-89-1(Hazardous Substances Data)

43024-89-1 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 43024-89-1 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 4,3,0,2 and 4 respectively; the second part has 2 digits, 8 and 9 respectively.
Calculate Digit Verification of CAS Registry Number 43024-89:
(7*4)+(6*3)+(5*0)+(4*2)+(3*4)+(2*8)+(1*9)=91
91 % 10 = 1
So 43024-89-1 is a valid CAS Registry Number.

43024-89-1Downstream Products

43024-89-1Relevant articles and documents

Synthesis and Enzymic Activity of 6-Carbethoxy- and 6-Ethoxy-3,7-disubstituted-pyrazolopyrimidines and Related Derivatives as Adenosine Cyclic 3',5'-Phosphate Phosphodiesterase Inhibitors

Springer, Robert H.,Scholten, M. B.,O'Brien, Darrell E.,Novinson, Thomas,Miller, Jon P.,Robins, Roland K.

, p. 235 - 242 (1982)

A number of 3,7-disubstituted 6-carbethoxypyrazolopyrimidines and 3,7-disubstituted 6-ethoxypyrazolopyrimidines have been prepared and evaluated as adenosine cyclic 3',5'-phosphate (cAMP) phosphodiesterase (PDE) inhibitors vs. the low Km enzyme isolated from beef heart, rabbit lung, and kidney preparations.The results were found to be between 0.5 to 13 times as potent as theophylline as inhibitors of PDE, depending on the tissue source.A number of these PDE inhibitors exhibited significant physiological effects in different animal systems, suggesting it should be possible to obtain selective PDE inhibition in various tissues.Several of these heterocycles were found superior to adenosine in inhibiting ADP-induced platelet aggregation in vitro.

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