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4-(6-allyl-benzo[1,3]dioxol-5-yl)-3-iodo-4-(3,4,5-trimethoxy-phenyl)-but-2-en-1-ol is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

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  • 685881-29-2 Structure
  • Basic information

    1. Product Name: 4-(6-allyl-benzo[1,3]dioxol-5-yl)-3-iodo-4-(3,4,5-trimethoxy-phenyl)-but-2-en-1-ol
    2. Synonyms: 4-(6-allyl-benzo[1,3]dioxol-5-yl)-3-iodo-4-(3,4,5-trimethoxy-phenyl)-but-2-en-1-ol
    3. CAS NO:685881-29-2
    4. Molecular Formula:
    5. Molecular Weight: 524.352
    6. EINECS: N/A
    7. Product Categories: N/A
    8. Mol File: 685881-29-2.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: 4-(6-allyl-benzo[1,3]dioxol-5-yl)-3-iodo-4-(3,4,5-trimethoxy-phenyl)-but-2-en-1-ol(CAS DataBase Reference)
    10. NIST Chemistry Reference: 4-(6-allyl-benzo[1,3]dioxol-5-yl)-3-iodo-4-(3,4,5-trimethoxy-phenyl)-but-2-en-1-ol(685881-29-2)
    11. EPA Substance Registry System: 4-(6-allyl-benzo[1,3]dioxol-5-yl)-3-iodo-4-(3,4,5-trimethoxy-phenyl)-but-2-en-1-ol(685881-29-2)
  • 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: 685881-29-2(Hazardous Substances Data)

685881-29-2 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 685881-29-2 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 6,8,5,8,8 and 1 respectively; the second part has 2 digits, 2 and 9 respectively.
Calculate Digit Verification of CAS Registry Number 685881-29:
(8*6)+(7*8)+(6*5)+(5*8)+(4*8)+(3*1)+(2*2)+(1*9)=222
222 % 10 = 2
So 685881-29-2 is a valid CAS Registry Number.

685881-29-2Downstream Products

685881-29-2Relevant articles and documents

Rhenium-catalyzed aromatic propargylation

Kennedy-Smith, Joshua J.,Young, Lauren A.,Toste, F. Dean

, p. 1325 - 1327 (2007/10/03)

A mild aromatic propargylation reaction, employing an air- and moisture-tolerant rhenium-oxo complex ((dppm)ReOCl3) as a catalyst and a propargyl alcohol as the electrophile, is described. The reaction tolerates a broad range of functional groups and regioselectively affords propargylic arenas without formation of the isomeric allenyl adducts. The potential of this rhenium(V)-catalyzed reaction is exemplified by application of the propargylation to the synthesis of O-methyldetrol, mimosifoliol, and β-apopicropodophyllin.

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