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1256556-06-5

C18H27O7P is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

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  • 1256556-06-5 Structure

  • Basic information

    1. Product Name: C18H27O7P
    2. Synonyms: C18H27O7P
    3. CAS NO:1256556-06-5
    4. Molecular Formula:
    5. Molecular Weight: 386.382
    6. EINECS: N/A
    7. Product Categories: N/A
    8. Mol File: 1256556-06-5.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: C18H27O7P(CAS DataBase Reference)
    10. NIST Chemistry Reference: C18H27O7P(1256556-06-5)
    11. EPA Substance Registry System: C18H27O7P(1256556-06-5)

  • 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: 1256556-06-5(Hazardous Substances Data)

1256556-06-5 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 1256556-06-5 includes 10 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 7 digits, 1,2,5,6,5,5 and 6 respectively; the second part has 2 digits, 0 and 6 respectively.
Calculate Digit Verification of CAS Registry Number 1256556-06:
(9*1)+(8*2)+(7*5)+(6*6)+(5*5)+(4*5)+(3*6)+(2*0)+(1*6)=165
165 % 10 = 5
So 1256556-06-5 is a valid CAS Registry Number.

1256556-06-5Upstream product

1256556-06-5Downstream Products

1256556-06-5Relevant articles and documents

Synthesis of the C(18)-C(34) fragment of amphidinolide C and the C(18)-C(29) fragment of amphidinolide F

Roy, Sudeshna,Spilling, Christopher D.

supporting information; experimental part, p. 5326 - 5329 (2011/01/05)

A convergent synthesis of the C(18)-C(34) fragment of amphidinolide C and the C(18)-C(29) fragment of amphidinolide F is reported. The approach involves the synthesis of the common intermediate tetrahydrofuranyl-β- ketophosphonate via cross metathesis, Pd

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