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(4S,5S)-4,5-Bis-benzyloxymethyl-2-((E)-4-furan-3-yl-1-methyl-but-1-enyl)-[1,3]dioxolane is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

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  • 125029-46-1 Structure
  • Basic information

    1. Product Name: (4S,5S)-4,5-Bis-benzyloxymethyl-2-((E)-4-furan-3-yl-1-methyl-but-1-enyl)-[1,3]dioxolane
    2. Synonyms: (4S,5S)-4,5-Bis-benzyloxymethyl-2-((E)-4-furan-3-yl-1-methyl-but-1-enyl)-[1,3]dioxolane
    3. CAS NO:125029-46-1
    4. Molecular Formula:
    5. Molecular Weight: 448.559
    6. EINECS: N/A
    7. Product Categories: N/A
    8. Mol File: 125029-46-1.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: (4S,5S)-4,5-Bis-benzyloxymethyl-2-((E)-4-furan-3-yl-1-methyl-but-1-enyl)-[1,3]dioxolane(CAS DataBase Reference)
    10. NIST Chemistry Reference: (4S,5S)-4,5-Bis-benzyloxymethyl-2-((E)-4-furan-3-yl-1-methyl-but-1-enyl)-[1,3]dioxolane(125029-46-1)
    11. EPA Substance Registry System: (4S,5S)-4,5-Bis-benzyloxymethyl-2-((E)-4-furan-3-yl-1-methyl-but-1-enyl)-[1,3]dioxolane(125029-46-1)
  • 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: 125029-46-1(Hazardous Substances Data)

125029-46-1 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 125029-46-1 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,2,5,0,2 and 9 respectively; the second part has 2 digits, 4 and 6 respectively.
Calculate Digit Verification of CAS Registry Number 125029-46:
(8*1)+(7*2)+(6*5)+(5*0)+(4*2)+(3*9)+(2*4)+(1*6)=101
101 % 10 = 1
So 125029-46-1 is a valid CAS Registry Number.

125029-46-1Downstream Products

125029-46-1Relevant articles and documents

CHIRAL INDUCTION IN A BIOMIMETIC OLEFIN CYCLIZATION

Takenaka, Hideyuki,Sato, Tomohiro,Nishizawa, Mugio

, p. 2267 - 2268 (1989)

Chiral induction has been achieved during a biomimetic cyclization of a chiral perillene derivatives in maximum 76percent diastereomeric excess.The absolute configuration of the predominant products are established by X-ray diffraction study and chemical transformations.

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