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851589-98-5

Pyrrolidine, 1-[(4-nitro-1H-pyrrol-2-yl)carbonyl]- is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

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  • 851589-98-5 Structure

  • Basic information

    1. Product Name: Pyrrolidine, 1-[(4-nitro-1H-pyrrol-2-yl)carbonyl]-
    2. Synonyms:
    3. CAS NO:851589-98-5
    4. Molecular Formula: C9H11N3O3
    5. Molecular Weight: 209.205
    6. EINECS: N/A
    7. Product Categories: N/A
    8. Mol File: 851589-98-5.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: Pyrrolidine, 1-[(4-nitro-1H-pyrrol-2-yl)carbonyl]-(CAS DataBase Reference)
    10. NIST Chemistry Reference: Pyrrolidine, 1-[(4-nitro-1H-pyrrol-2-yl)carbonyl]-(851589-98-5)
    11. EPA Substance Registry System: Pyrrolidine, 1-[(4-nitro-1H-pyrrol-2-yl)carbonyl]-(851589-98-5)

  • 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: 851589-98-5(Hazardous Substances Data)

851589-98-5 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 851589-98-5 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 8,5,1,5,8 and 9 respectively; the second part has 2 digits, 9 and 8 respectively.
Calculate Digit Verification of CAS Registry Number 851589-98:
(8*8)+(7*5)+(6*1)+(5*5)+(4*8)+(3*9)+(2*9)+(1*8)=215
215 % 10 = 5
So 851589-98-5 is a valid CAS Registry Number.

851589-98-5Relevant articles and documents

Novel non-steroidal/non-anilide type androgen antagonists: Discovery of 4-substituted pyrrole-2-carboxamides as a new scaffold for androgen receptor ligands

Wakabayashi, Ken-Ichi,Miyachi, Hiroyuki,Hashimoto, Yuichi,Tanatani, Aya

, p. 2837 - 2846 (2007/10/03)

We designed and synthesized novel pyrrole-2-carboxamide derivatives as androgen antagonists. Compounds 10 and 13 bearing benzylamine or aniline at the 4-position of the pyrrole ring showed moderate androgen antagonistic activity, and inhibited the androgen-dependent growth of Shionogi carcinoma cells (SC-3). Study of the structure-activity relationships of compound 13 led to a potent androgen antagonist 36, which has higher affinity than flutamide (4) for androgen nuclear receptor (AR). Thus, pyrrole-2-carboxamide is a new scaffold for developing AR antagonists.

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