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6-[(2-AMINOETHYL)AMINO]-7-CHLORO-1-CYCLOPROPYL-1,4-DIHYDRO-4-OXO-QUINOLINE-3-CARBOXYLIC ACID is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

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  • 6-[(2-Aminoethyl)amino]-7-chloro-1-cyclopropyl-1,4-dihydro-4-oxo-quinoline-3-carboxylic acid

    Cas No: 528851-85-6

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  • 6-[(2-AMINOETHYL)AMINO]-7-CHLORO-1-CYCLOPROPYL-1,4-DIHYDRO-4-OXO-QUINOLINE-3-CARBOXYLIC ACID

    Cas No: 528851-85-6

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  • 528851-85-6 Structure
  • Basic information

    1. Product Name: 6-[(2-AMINOETHYL)AMINO]-7-CHLORO-1-CYCLOPROPYL-1,4-DIHYDRO-4-OXO-QUINOLINE-3-CARBOXYLIC ACID
    2. Synonyms: 6-[(2-AMINOETHYL)AMINO]-7-CHLORO-1-CYCLOPROPYL-1,4-DIHYDRO-4-OXO-QUINOLINE-3-CARBOXYLIC ACID;Ciprofloxacin Impurity 2
    3. CAS NO:528851-85-6
    4. Molecular Formula: C15H16ClN3O3
    5. Molecular Weight: 321.75884
    6. EINECS: N/A
    7. Product Categories: Aromatics Compounds;Aromatics;Miscellaneous Reagents;Amines;Heterocycles
    8. Mol File: 528851-85-6.mol
  • Chemical Properties

    1. Melting Point: N/A
    2. Boiling Point: 583.1 °C at 760 mmHg
    3. Flash Point: 306.5 °C
    4. Appearance: Yellow powder
    5. Density: 1.563 g/cm3
    6. Refractive Index: N/A
    7. Storage Temp.: N/A
    8. Solubility: DMSO
    9. PKA: 6.41±0.41(Predicted)
    10. CAS DataBase Reference: 6-[(2-AMINOETHYL)AMINO]-7-CHLORO-1-CYCLOPROPYL-1,4-DIHYDRO-4-OXO-QUINOLINE-3-CARBOXYLIC ACID(CAS DataBase Reference)
    11. NIST Chemistry Reference: 6-[(2-AMINOETHYL)AMINO]-7-CHLORO-1-CYCLOPROPYL-1,4-DIHYDRO-4-OXO-QUINOLINE-3-CARBOXYLIC ACID(528851-85-6)
    12. EPA Substance Registry System: 6-[(2-AMINOETHYL)AMINO]-7-CHLORO-1-CYCLOPROPYL-1,4-DIHYDRO-4-OXO-QUINOLINE-3-CARBOXYLIC ACID(528851-85-6)
  • 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: 528851-85-6(Hazardous Substances Data)

528851-85-6 Usage

Chemical Properties

Yellow Powder

Check Digit Verification of cas no

The CAS Registry Mumber 528851-85-6 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 5,2,8,8,5 and 1 respectively; the second part has 2 digits, 8 and 5 respectively.
Calculate Digit Verification of CAS Registry Number 528851-85:
(8*5)+(7*2)+(6*8)+(5*8)+(4*5)+(3*1)+(2*8)+(1*5)=186
186 % 10 = 6
So 528851-85-6 is a valid CAS Registry Number.

528851-85-6SDS

SAFETY DATA SHEETS

According to Globally Harmonized System of Classification and Labelling of Chemicals (GHS) - Sixth revised edition

Version: 1.0

Creation Date: Aug 19, 2017

Revision Date: Aug 19, 2017

1.Identification

1.1 GHS Product identifier

Product name 6-(2-aminoethylamino)-7-chloro-1-cyclopropyl-4-oxoquinoline-3-carboxylic acid

1.2 Other means of identification

Product number -
Other names -

1.3 Recommended use of the chemical and restrictions on use

Identified uses For industry use only.
Uses advised against no data available

1.4 Supplier's details

1.5 Emergency phone number

Emergency phone number -
Service hours Monday to Friday, 9am-5pm (Standard time zone: UTC/GMT +8 hours).

More Details:528851-85-6 SDS

528851-85-6Downstream Products

528851-85-6Relevant articles and documents

Synthesis and antibacterial evaluation of novel 4′-glycyl linked quinolyl-azithromycins with potent activity against macrolide-resistant pathogens

Pavlovi?, Dra?en,Mutak, Stjepan

, p. 1255 - 1267 (2016/03/01)

A new azithromycin-based series of antibacterial macrolones is reported, which features the use of a 4′-ester linked glycin for tethering the quinolone side chain to the macrolide scaffold. Among the analogs prepared, compounds 9e and 22f with a quinolon-6-yl moiety were found to have potent and well-balanced activity against clinically important respiratory tract pathogens, including erythromycin-susceptible and MLSB resistant strains of Streptococcus pneumoniae, Streptococcus pyogenes, and Haemophilus influenzae. In addition, potential lead compounds 9e and 22f demonstrated outstanding levels of activity against Moraxella catarrhalis and inducibly MLSB resistant Staphylococcus aureus. The best member of this series 22f rivals or exceeds, in potency, some of the most active ketolide antibacterial agents known today, such as telithromycin and cethromycin.

NOVEL 14 AND 15 MEMBERED-RING COMPOUNDS

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Page 35, (2008/06/13)

The present invention relates to 14- or 15-membered macrolides substituted at the 4" position of formula (I) and pharmaceutically acceptable derivatives thereof, to processes for their preparation and their use in therapy or prophylaxis of systemic or topical microbial infections in a human or animal body.

MACROLIDES SUBSTITUTED AT THE 3-POSITION HAVING ANTIMICROBIAL ACTIVITY

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Page 29, (2010/02/09)

The present invention relates to 14- or 15-membered macrolides substituted at the 3-position of formula (I) and pharmaceutically acceptable derivatives thereof, to processes for their preparation and their use in therapy or prophylaxis of systemic or topi

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