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CAS

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183722-50-1

(4aR,8aS)-2-(4-Methoxy-phenyl)-hexahydro-pyrano[3,2-d][1,3]dioxine is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

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  • 183722-50-1 Structure

  • Basic information

    1. Product Name: (4aR,8aS)-2-(4-Methoxy-phenyl)-hexahydro-pyrano[3,2-d][1,3]dioxine
    2. Synonyms: (4aR,8aS)-2-(4-Methoxy-phenyl)-hexahydro-pyrano[3,2-d][1,3]dioxine
    3. CAS NO:183722-50-1
    4. Molecular Formula:
    5. Molecular Weight: 250.295
    6. EINECS: N/A
    7. Product Categories: N/A
    8. Mol File: 183722-50-1.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: (4aR,8aS)-2-(4-Methoxy-phenyl)-hexahydro-pyrano[3,2-d][1,3]dioxine(CAS DataBase Reference)
    10. NIST Chemistry Reference: (4aR,8aS)-2-(4-Methoxy-phenyl)-hexahydro-pyrano[3,2-d][1,3]dioxine(183722-50-1)
    11. EPA Substance Registry System: (4aR,8aS)-2-(4-Methoxy-phenyl)-hexahydro-pyrano[3,2-d][1,3]dioxine(183722-50-1)

  • 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: 183722-50-1(Hazardous Substances Data)

183722-50-1 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 183722-50-1 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,8,3,7,2 and 2 respectively; the second part has 2 digits, 5 and 0 respectively.
Calculate Digit Verification of CAS Registry Number 183722-50:
(8*1)+(7*8)+(6*3)+(5*7)+(4*2)+(3*2)+(2*5)+(1*0)=141
141 % 10 = 1
So 183722-50-1 is a valid CAS Registry Number.

183722-50-1Relevant articles and documents

Convergent synthesis of the FGHI ring segment of yessotoxin

Kadota, Isao,Ueno, Hirokazu,Sato, Yuki,Yamamoto, Yoshinori

, p. 89 - 92 (2006)

A convergent synthesis of the FGHI ring segment of yessotoxin was achieved via the intramolecular allylation of an α-chloroacetoxy ether and subsequent ring-closing metathesis.

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