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1036595-92-2

4-chloro-N-cyclopentyl-2-nitroaniline is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

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  • 1036595-92-2 Structure

  • Basic information

    1. Product Name: 4-chloro-N-cyclopentyl-2-nitroaniline
    2. Synonyms:
    3. CAS NO:1036595-92-2
    4. Molecular Formula:
    5. Molecular Weight: 240.689
    6. EINECS: N/A
    7. Product Categories: N/A
    8. Mol File: 1036595-92-2.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: 4-chloro-N-cyclopentyl-2-nitroaniline(CAS DataBase Reference)
    10. NIST Chemistry Reference: 4-chloro-N-cyclopentyl-2-nitroaniline(1036595-92-2)
    11. EPA Substance Registry System: 4-chloro-N-cyclopentyl-2-nitroaniline(1036595-92-2)

  • 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: 1036595-92-2(Hazardous Substances Data)

1036595-92-2 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 1036595-92-2 includes 10 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 7 digits, 1,0,3,6,5,9 and 5 respectively; the second part has 2 digits, 9 and 2 respectively.
Calculate Digit Verification of CAS Registry Number 1036595-92:
(9*1)+(8*0)+(7*3)+(6*6)+(5*5)+(4*9)+(3*5)+(2*9)+(1*2)=162
162 % 10 = 2
So 1036595-92-2 is a valid CAS Registry Number.

1036595-92-2Downstream Products

1036595-92-2Relevant articles and documents

Synthesis and in vitro antimicrobial activity of some novel substituted benzimidazole derivatives having potent activity against MRSA

Tuncbilek, Meral,Kiper, Tulug,Altanlar, Nurten

experimental part, p. 1024 - 1033 (2009/09/06)

The novel benzimidazole derivatives (3, 5, 8, 9, 12-14, 18-41) were prepared in this paper and the antimicrobial activities of these compounds against Staphylococcus aureus, methicillin-resistant S. aureus (MRSA, standard and clinical isolates), Bacillus subtilis, Escherichia coli and Candida albicans were evaluated. Compounds 24-26 which have no substitution of N-1 position displayed better antibacterial activities than those of standards (ciprofloxacin, ampicillin and sultamicillin) against both the drug-resistant bacteria (MRSA, standard and clinical isolates). These derivatives (24-26), 2,5,6-trihalogenobenzimidazole analogues (8, 12), 5,6-dichloro-2-amino derivative (13), and 5-chloro-2-(4-benzyloxyphenyl)benzimidazole (35) exhibited the most potent antibacterial activity with MIC 3.12 μg/ml against S. aureus.

Design and syntheses of a series of novel serotonin3 antagonists

Hori,Suzuki,Yamamoto,Nakajima,Ozaki,Ohtaka

, p. 1832 - 1841 (2007/10/02)

From a structural comparison study between serotonin and serotonin3 (5- HT3) antagonists using a two-dimensional grid template composed of regular hexagons, we deduced structural modification patterns from agonists to antagonists, an

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