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CAS

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389634-44-0

(2R,3R)-1,4-dimethoxy-1,1,4,4-tetraphenyl-2,3-butanediol (R)-2-(1-hydroxybutyl)-3-furanylboronate is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

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  • 389634-44-0 Structure

  • Basic information

    1. Product Name: (2R,3R)-1,4-dimethoxy-1,1,4,4-tetraphenyl-2,3-butanediol (R)-2-(1-hydroxybutyl)-3-furanylboronate
    2. Synonyms:
    3. CAS NO:389634-44-0
    4. Molecular Formula:
    5. Molecular Weight: 602.535
    6. EINECS: N/A
    7. Product Categories: N/A
    8. Mol File: 389634-44-0.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: (2R,3R)-1,4-dimethoxy-1,1,4,4-tetraphenyl-2,3-butanediol (R)-2-(1-hydroxybutyl)-3-furanylboronate(CAS DataBase Reference)
    10. NIST Chemistry Reference: (2R,3R)-1,4-dimethoxy-1,1,4,4-tetraphenyl-2,3-butanediol (R)-2-(1-hydroxybutyl)-3-furanylboronate(389634-44-0)
    11. EPA Substance Registry System: (2R,3R)-1,4-dimethoxy-1,1,4,4-tetraphenyl-2,3-butanediol (R)-2-(1-hydroxybutyl)-3-furanylboronate(389634-44-0)

  • 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: 389634-44-0(Hazardous Substances Data)

389634-44-0 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 389634-44-0 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 3,8,9,6,3 and 4 respectively; the second part has 2 digits, 4 and 4 respectively.
Calculate Digit Verification of CAS Registry Number 389634-44:
(8*3)+(7*8)+(6*9)+(5*6)+(4*3)+(3*4)+(2*4)+(1*4)=200
200 % 10 = 0
So 389634-44-0 is a valid CAS Registry Number.

389634-44-0Downstream Products

389634-44-0Relevant articles and documents

Diastereoselective addition reactions of furyl aldehydes using chiral boronates as auxiliary: Application to the enantioselective synthesis of 2,3-disubstituted furyl alcohols

Chan, Kin-Fai,Wong, Henry N. C.

, p. 3991 - 3994 (2001)

matrix presented The addition reactions of various nucleophiles to a furyl aldehyde bearing a chiral boronate at the C-3 position furnished chromatographically separable diastereomers. The R diastereoselection was more favorable when no additive was added

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