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CAS

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35975-93-0

6-benzyl-4-oxo-1,4-dihydroquinoline-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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  • 35975-93-0 Structure

  • Basic information

    1. Product Name: 6-benzyl-4-oxo-1,4-dihydroquinoline-3-carboxylic acid
    2. Synonyms:
    3. CAS NO:35975-93-0
    4. Molecular Formula:
    5. Molecular Weight: 279.295
    6. EINECS: N/A
    7. Product Categories: N/A
    8. Mol File: 35975-93-0.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: 6-benzyl-4-oxo-1,4-dihydroquinoline-3-carboxylic acid(CAS DataBase Reference)
    10. NIST Chemistry Reference: 6-benzyl-4-oxo-1,4-dihydroquinoline-3-carboxylic acid(35975-93-0)
    11. EPA Substance Registry System: 6-benzyl-4-oxo-1,4-dihydroquinoline-3-carboxylic acid(35975-93-0)

  • 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: 35975-93-0(Hazardous Substances Data)

35975-93-0 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 35975-93-0 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 3,5,9,7 and 5 respectively; the second part has 2 digits, 9 and 3 respectively.
Calculate Digit Verification of CAS Registry Number 35975-93:
(7*3)+(6*5)+(5*9)+(4*7)+(3*5)+(2*9)+(1*3)=160
160 % 10 = 0
So 35975-93-0 is a valid CAS Registry Number.

35975-93-0Relevant articles and documents

Investigating the role of metal chelation in HIV-1 integrase strand transfer inhibitors

Bacchi, Alessia,Carcelli, Mauro,Compari, Carlotta,Fisicaro, Emilia,Pala, Nicolino,Rispoli, Gabriele,Rogolino, Dominga,Sanchez, Tino W.,Sechi, Mario,Sinisi, Valentina,Neamati, Nouri

, p. 8407 - 8420 (2011)

HIV-1 integrase (IN) has been validated as an attractive target for the treatment of HIV/AIDS. Several studies have confirmed that the metal binding function is a crucial feature in many of the reported IN inhibitors. To provide new insights on the metal

Novel HIV-1 integrase inhibitors derived from quinolone antibiotics

Sato, Motohide,Motomura, Takahisa,Aramaki, Hisateru,Matsuda, Takashi,Yamashita, Masaki,Ito, Yoshiharu,Kawakami, Hiroshi,Matsuzaki, Yuji,Watanabe, Wataru,Yamataka, Kazunobu,Ikeda, Satoru,Kodama, Eiichi,Matsuoka, Masao,Shinkai, Hisashi

, p. 1506 - 1508 (2007/10/03)

The viral enzyme integrase is essential for the replication of human immunodeficiency virus type 1 (HIV-1) and represents a remaining target for antiretroviral drugs. Here, we describe the modification of a quinolone antibiotic to produce the novel integr

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