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1607826-45-8

methyl (2S,3R)-3-(4-(benzyloxy)phenyl)-2,3-dihydroxypropanoate is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

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  • 1607826-45-8 Structure

  • Basic information

    1. Product Name: methyl (2S,3R)-3-(4-(benzyloxy)phenyl)-2,3-dihydroxypropanoate
    2. Synonyms: methyl (2S,3R)-3-(4-(benzyloxy)phenyl)-2,3-dihydroxypropanoate
    3. CAS NO:1607826-45-8
    4. Molecular Formula:
    5. Molecular Weight: 302.327
    6. EINECS: N/A
    7. Product Categories: N/A
    8. Mol File: 1607826-45-8.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: methyl (2S,3R)-3-(4-(benzyloxy)phenyl)-2,3-dihydroxypropanoate(CAS DataBase Reference)
    10. NIST Chemistry Reference: methyl (2S,3R)-3-(4-(benzyloxy)phenyl)-2,3-dihydroxypropanoate(1607826-45-8)
    11. EPA Substance Registry System: methyl (2S,3R)-3-(4-(benzyloxy)phenyl)-2,3-dihydroxypropanoate(1607826-45-8)

  • 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: 1607826-45-8(Hazardous Substances Data)

1607826-45-8 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 1607826-45-8 includes 10 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 7 digits, 1,6,0,7,8,2 and 6 respectively; the second part has 2 digits, 4 and 5 respectively.
Calculate Digit Verification of CAS Registry Number 1607826-45:
(9*1)+(8*6)+(7*0)+(6*7)+(5*8)+(4*2)+(3*6)+(2*4)+(1*5)=178
178 % 10 = 8
So 1607826-45-8 is a valid CAS Registry Number.

1607826-45-8Relevant articles and documents

Stellatolides, a new cyclodepsipeptide family from the sponge ecionemia acervus: Isolation, solid-phase total synthesis, and full structural assignment of stellatolide a

Martin, Maria Jesus,Rodriguez-Acebes, Raquel,Garcia-Ramos, Yésica,Martinez, Valentin,Murcia, Carmen,Digon, Isabel,Marco, Isabel,Pelay-Gimeno, Marta,Fernández, Rogelio,Reyes, Fernando,Francesch, Andrés M.,Munt, Simon,Tulla-Puche, Judit,Albericio, Fernando,Cuevas, Carmen

supporting information, p. 6754 - 6762 (2014/05/20)

The marine environment is a rich source of metabolites with potential therapeutic properties and applications for humans. Here we describe the first isolation, solid-phase total synthesis, and full structural assignment of a new class of cyclodepsipeptides from the Madagascan sponge Ecionemia acervus that shows in vitro cytotoxic activities at submicromolar concentrations. Seven structures belonging to a new family of compounds, given the general name stellatolides, were characterized. The sequence and stereochemistry of all the amino acids in these molecules were established by a combination of spectroscopic analysis, chemical degradation, and derivatization studies. Furthermore, the complete structure of stellatolide A was confirmed by an efficient solid-phase method for the first total synthesis and the full structural assignment of this molecule, including the asymmetric synthesis of the unique B-hydroxy acid moiety (Z)-3-hydroxy-6,8-dimethylnon-4-enoic acid.

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