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574-05-0

(6aS)-5,6a,7,8,9,11-Hexahydro-6β,11β-methano-8α-methoxy-6H-1,3-benzodioxolo[5,6-c][1]benzoazepine-9β-ol is a complex organic compound with a molecular formula of C18H19NO3. It is a derivative of benzodioxole and benzazepine, featuring a hexahydro structure with a methano bridge between the 6β and 11β positions. The compound also has a methoxy group at the 8α position and a hydroxyl group at the 9β position. This chemical is known for its potential applications in the pharmaceutical industry, particularly as a precursor in the synthesis of certain drugs. Its structure provides a unique set of properties that can be exploited for various therapeutic purposes, although further research is needed to fully understand its potential uses and effects.

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  • 574-05-0 Structure

  • Basic information

    1. Product Name: (6aS)-5,6a,7,8,9,11-Hexahydro-6β,11β-methano-8α-methoxy-6H-1,3-benzodioxolo[5,6-c][1]benzoazepine-9β-ol
    2. Synonyms: (6aS)-5,6a,7,8,9,11-Hexahydro-6β,11β-methano-8α-methoxy-6H-1,3-benzodioxolo[5,6-c][1]benzoazepine-9β-ol;3-O-Methylpancracine;Isohemanthamine
    3. CAS NO:574-05-0
    4. Molecular Formula: C17H19NO4
    5. Molecular Weight: 301.33706
    6. EINECS: N/A
    7. Product Categories: N/A
    8. Mol File: 574-05-0.mol

  • Chemical Properties

    1. Melting Point: N/A
    2. Boiling Point: N/A
    3. Flash Point: N/A
    4. Appearance: /
    5. Density: N/A
    6. Refractive Index: N/A
    7. Storage Temp.: N/A
    8. Solubility: N/A
    9. CAS DataBase Reference: (6aS)-5,6a,7,8,9,11-Hexahydro-6β,11β-methano-8α-methoxy-6H-1,3-benzodioxolo[5,6-c][1]benzoazepine-9β-ol(CAS DataBase Reference)
    10. NIST Chemistry Reference: (6aS)-5,6a,7,8,9,11-Hexahydro-6β,11β-methano-8α-methoxy-6H-1,3-benzodioxolo[5,6-c][1]benzoazepine-9β-ol(574-05-0)
    11. EPA Substance Registry System: (6aS)-5,6a,7,8,9,11-Hexahydro-6β,11β-methano-8α-methoxy-6H-1,3-benzodioxolo[5,6-c][1]benzoazepine-9β-ol(574-05-0)

  • 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: 574-05-0(Hazardous Substances Data)

574-05-0 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 574-05-0 includes 6 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 3 digits, 5,7 and 4 respectively; the second part has 2 digits, 0 and 5 respectively.
Calculate Digit Verification of CAS Registry Number 574-05:
(5*5)+(4*7)+(3*4)+(2*0)+(1*5)=70
70 % 10 = 0
So 574-05-0 is a valid CAS Registry Number.

574-05-0Relevant articles and documents

Synthetic analogues of the montanine-type alkaloids with activity against apoptosis-resistant cancer cells

Govindaraju, Karthik,Ingels, Aude,Hasan, Md Nabiul,Sun, Dandan,Mathieu, Veronique,Masi, Marco,Evidente, Antonio,Kornienko, Alexander

, p. 589 - 593 (2018/02/09)

In a search of small molecules active against apoptosis-resistant cancer cells, a skeletal rearrangement of alkaloid haemanthamine was utilized to generate a series of compounds possessing the alkaloid montanine ring system. The synthesized compounds were found to inhibit proliferation of cancer cells resistant to apoptosis at micromolar concentrations. Selected compounds were also active against patient-derived glioblastoma cells expressing stem-cell markers. This is the first report describing the preparation of synthetic analogues of the montanine-type alkaloids with antiproliferative activity. The compounds prepared in the current investigation appear to be a useful starting point for the development of agents to fight cancers with apoptosis resistance, and thus, associated with poor prognoses.

An expedient route to montanine-type amaryllidaceae alkaloids: Total syntheses of (-)-brunsvigine and (-)-manthine

Hong, An-Wei,Cheng, Tsung-Hui,Raghukumar, Vellingiri,Sha, Chin-Kang

, p. 7580 - 7585 (2008/12/22)

(Chemical Equation Presented) The first total syntheses of (-)-brunsvigine (1) and (-)-manthine (2) were accomplished in 10 and 18 steps, respectively. (-)-Quinic acid was converted to enone 12 in live steps. Iodination of enone 12 followed by stereoselec

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