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CAS

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1310575-44-0

6-hydroxy-1-(3-methoxyphenyl)-2-propyl-2,3,4,9-tetrahydro-1H-β-carboline hydrochloride is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

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  • 1310575-44-0 Structure

  • Basic information

    1. Product Name: 6-hydroxy-1-(3-methoxyphenyl)-2-propyl-2,3,4,9-tetrahydro-1H-β-carboline hydrochloride
    2. Synonyms: 6-hydroxy-1-(3-methoxyphenyl)-2-propyl-2,3,4,9-tetrahydro-1H-β-carboline hydrochloride
    3. CAS NO:1310575-44-0
    4. Molecular Formula:
    5. Molecular Weight: 336.434
    6. EINECS: N/A
    7. Product Categories: N/A
    8. Mol File: 1310575-44-0.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-hydroxy-1-(3-methoxyphenyl)-2-propyl-2,3,4,9-tetrahydro-1H-β-carboline hydrochloride(CAS DataBase Reference)
    10. NIST Chemistry Reference: 6-hydroxy-1-(3-methoxyphenyl)-2-propyl-2,3,4,9-tetrahydro-1H-β-carboline hydrochloride(1310575-44-0)
    11. EPA Substance Registry System: 6-hydroxy-1-(3-methoxyphenyl)-2-propyl-2,3,4,9-tetrahydro-1H-β-carboline hydrochloride(1310575-44-0)

  • 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: 1310575-44-0(Hazardous Substances Data)

1310575-44-0 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 1310575-44-0 includes 10 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 7 digits, 1,3,1,0,5,7 and 5 respectively; the second part has 2 digits, 4 and 4 respectively.
Calculate Digit Verification of CAS Registry Number 1310575-44:
(9*1)+(8*3)+(7*1)+(6*0)+(5*5)+(4*7)+(3*5)+(2*4)+(1*4)=120
120 % 10 = 0
So 1310575-44-0 is a valid CAS Registry Number.

1310575-44-0Downstream Products

1310575-44-0Relevant articles and documents

Antioxydant activity of β-carboline derivatives in the LDL oxidation model

Hadjaz, Fariza,Besret, Soizic,Martin-Nizard, Fran?oise,Yous, Sa?d,Dilly, Sébastien,Lebegue, Nicolas,Chavatte, Philippe,Duriez, Patrick,Berthelot, Pascal,Carato, Pascal

, p. 2575 - 2585 (2011/06/23)

A series of β-carboline compounds were synthesized, starting from compound GWC22, their antioxidant activity was determined by inhibition of lipid peroxidation. The oxidation of LDL was induced in the presence of CuSO 4 or 2,2′-azobis(2-amidinopropane) dihydrochloride (AAPH). The protective actions of these compounds against the cytotoxicity were evaluated with lactate dehydrogenase (LDH) activity in bovine aortic endothelial cells (BAECs) and cellular vitality by measuring mitochondrial activity in the presence of MTT (3-(4,5-dimethylthiazol-2-yl)-2,5-diphenyltetrazolium bromide). Most of compounds showed an higher antioxidant activity than GWC22 derivative (R = 1.6 for 5 μM CuSO4). The best antioxidant activities are phenolic and benzyloxy derivatives with ratio R = 1.9 to 2.8 for 1 μM CuSO4. These substances have protective actions and increase significantly the cell viability.

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