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CAS

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60464-10-0

cis-Nephrosterinsaeure is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

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  • 60464-10-0 Structure

  • Basic information

    1. Product Name: cis-Nephrosterinsaeure
    2. Synonyms:
    3. CAS NO:60464-10-0
    4. Molecular Formula:
    5. Molecular Weight: 296.407
    6. EINECS: N/A
    7. Product Categories: N/A
    8. Mol File: 60464-10-0.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: cis-Nephrosterinsaeure(CAS DataBase Reference)
    10. NIST Chemistry Reference: cis-Nephrosterinsaeure(60464-10-0)
    11. EPA Substance Registry System: cis-Nephrosterinsaeure(60464-10-0)

  • 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: 60464-10-0(Hazardous Substances Data)

60464-10-0 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 60464-10-0 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 6,0,4,6 and 4 respectively; the second part has 2 digits, 1 and 0 respectively.
Calculate Digit Verification of CAS Registry Number 60464-10:
(7*6)+(6*0)+(5*4)+(4*6)+(3*4)+(2*1)+(1*0)=100
100 % 10 = 0
So 60464-10-0 is a valid CAS Registry Number.

60464-10-0Downstream Products

60464-10-0Relevant articles and documents

Synthesis of both enantiomers of methylenolactocin, nephrosterinic acid and protolichesterinic acid via tandem aldol-lactonization reactions

Kongsaeree, Palangpon,Meepowpan, Puttinan,Thebtaranonth, Yodhathai

, p. 1913 - 1922 (2001)

Both forms of the enantiomerically pure methylenolactocin, nephrosterinic and protolichesterinic acid have been synthesized via tandem aldol-lactonization reactions from corresponding optically active itaconate-anthracene adducts.

Enzymatic resolution of α-methyleneparaconic acids and evaluation of their biological activity

Chakrabarty, Kuheli,Defrenza, Ivana,Denora, Nunzio,Drioli, Sara,Forzato, Cristina,Franco, Massimo,Lentini, Giovanni,Nitti, Patrizia,Pitacco, Giuliana

, p. 239 - 246 (2015/03/18)

Both enantiomers of three biologically relevant paraconic acids-MB-3, methylenolactocin, and C75-were obtained with enantioselectivities up to 99% by kinetic enzymatic resolutions. Good enantiomeric excesses were obtained for MB-3 and methylenolactocin, using α-chymotrypsin and aminoacylase as enantiocomplementary enzymes, while C75 was resolved with aminoacylase. They all were evaluated for their antiproliferative, antibacterial, and antifungal activities, showing weak effects and practically no difference between enantiomers in each case. At high concentrations (16-64μg/mL), (-)- C75 acted as an antimicrobial agent against Gram-positive bacteria.

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