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ethyl (4S,5S)-4-(4-methoxybenzyloxy)-5-formyloxy-7-phenyl-(2Z)-heptenoate is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

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  • 700871-03-0 Structure
  • Basic information

    1. Product Name: ethyl (4S,5S)-4-(4-methoxybenzyloxy)-5-formyloxy-7-phenyl-(2Z)-heptenoate
    2. Synonyms: ethyl (4S,5S)-4-(4-methoxybenzyloxy)-5-formyloxy-7-phenyl-(2Z)-heptenoate
    3. CAS NO:700871-03-0
    4. Molecular Formula:
    5. Molecular Weight: 412.483
    6. EINECS: N/A
    7. Product Categories: N/A
    8. Mol File: 700871-03-0.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: ethyl (4S,5S)-4-(4-methoxybenzyloxy)-5-formyloxy-7-phenyl-(2Z)-heptenoate(CAS DataBase Reference)
    10. NIST Chemistry Reference: ethyl (4S,5S)-4-(4-methoxybenzyloxy)-5-formyloxy-7-phenyl-(2Z)-heptenoate(700871-03-0)
    11. EPA Substance Registry System: ethyl (4S,5S)-4-(4-methoxybenzyloxy)-5-formyloxy-7-phenyl-(2Z)-heptenoate(700871-03-0)
  • 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: 700871-03-0(Hazardous Substances Data)

700871-03-0 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 700871-03-0 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 7,0,0,8,7 and 1 respectively; the second part has 2 digits, 0 and 3 respectively.
Calculate Digit Verification of CAS Registry Number 700871-03:
(8*7)+(7*0)+(6*0)+(5*8)+(4*7)+(3*1)+(2*0)+(1*3)=130
130 % 10 = 0
So 700871-03-0 is a valid CAS Registry Number.

700871-03-0Downstream Products

700871-03-0Relevant articles and documents

Facile One-Step Synthesis of β-Alkoxy Lactone via Sequential Lactonization and 1,4-Addition of Alkoxide Group: Total Synthesis of All Stereoisomers of Dihydrokawain-5-ol

Singh, Ravi P.,Singh, Vinod K.

, p. 3425 - 3430 (2007/10/03)

We describe here a divergent total synthesis of all of the four stereoisomers of dihydrokawain-5-ol starting from α-D-glucose. The approach involves the use of Ando's modification of Horner-Wadsworth-Emmons homologation to give a α,β-unsaturated ester. Subsequently, lactonization and 1,4-addition of OMe group in one step provided a γ-lactone, which was converted into the target compounds in two steps.

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