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1228447-69-5

(E,3R,5R)-7-(methoxycarbonyl)-5-hydroxy-3-methylhept-6-enyl benzoate is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

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  • (E,3R,5R)-7-(methoxycarbonyl)-5-hydroxy-3-methylhept-6-enyl benzoate

    Cas No: 1228447-69-5

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  • 1228447-69-5 Structure

  • Basic information

    1. Product Name: (E,3R,5R)-7-(methoxycarbonyl)-5-hydroxy-3-methylhept-6-enyl benzoate
    2. Synonyms: (E,3R,5R)-7-(methoxycarbonyl)-5-hydroxy-3-methylhept-6-enyl benzoate
    3. CAS NO:1228447-69-5
    4. Molecular Formula:
    5. Molecular Weight: 306.359
    6. EINECS: N/A
    7. Product Categories: N/A
    8. Mol File: 1228447-69-5.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: (E,3R,5R)-7-(methoxycarbonyl)-5-hydroxy-3-methylhept-6-enyl benzoate(CAS DataBase Reference)
    10. NIST Chemistry Reference: (E,3R,5R)-7-(methoxycarbonyl)-5-hydroxy-3-methylhept-6-enyl benzoate(1228447-69-5)
    11. EPA Substance Registry System: (E,3R,5R)-7-(methoxycarbonyl)-5-hydroxy-3-methylhept-6-enyl benzoate(1228447-69-5)

  • 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: 1228447-69-5(Hazardous Substances Data)

1228447-69-5 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 1228447-69-5 includes 10 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 7 digits, 1,2,2,8,4,4 and 7 respectively; the second part has 2 digits, 6 and 9 respectively.
Calculate Digit Verification of CAS Registry Number 1228447-69:
(9*1)+(8*2)+(7*2)+(6*8)+(5*4)+(4*4)+(3*7)+(2*6)+(1*9)=165
165 % 10 = 5
So 1228447-69-5 is a valid CAS Registry Number.

1228447-69-5Relevant articles and documents

Enhancement of antiproliferative activity by molecular simplification of catalpol

García, Celina,León, Leticia G.,Pungitore, Carlos R.,Ríos-Luci, Carla,Daranas, Antonio H.,Montero, Juan C.,Pandiella, Atanasio,Tonn, Carlos E.,Martín, Víctor S.,Padrón, José M.

experimental part, p. 2515 - 2523 (2010/06/17)

Two iridoid scaffolds were synthesized enantioselectively using as key step an l-proline-catalyzed α-formyl oxidation. The in vitro antiproliferative activities were evaluated against a representative panel of human solid tumor cell lines. Both iridoids induced considerably growth inhibition in the range 0.38-1.86 μM. Cell cycle studies for these compounds showed the induction of cell cycle arrest at the G1 phase. This result was consistent with a decrease in the expression of cyclin D1. Damaged cells underwent apoptosis as indicated by specific Annexin V staining.

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