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2-((2R,3R,4R)-3,4-Bis-benzyloxy-5-methoxy-2-methyl-tetrahydro-furan-2-yl)-ethanol is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

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  • 887769-08-6 Structure
  • Basic information

    1. Product Name: 2-((2R,3R,4R)-3,4-Bis-benzyloxy-5-methoxy-2-methyl-tetrahydro-furan-2-yl)-ethanol
    2. Synonyms: 2-((2R,3R,4R)-3,4-Bis-benzyloxy-5-methoxy-2-methyl-tetrahydro-furan-2-yl)-ethanol
    3. CAS NO:887769-08-6
    4. Molecular Formula:
    5. Molecular Weight: 372.461
    6. EINECS: N/A
    7. Product Categories: N/A
    8. Mol File: 887769-08-6.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: 2-((2R,3R,4R)-3,4-Bis-benzyloxy-5-methoxy-2-methyl-tetrahydro-furan-2-yl)-ethanol(CAS DataBase Reference)
    10. NIST Chemistry Reference: 2-((2R,3R,4R)-3,4-Bis-benzyloxy-5-methoxy-2-methyl-tetrahydro-furan-2-yl)-ethanol(887769-08-6)
    11. EPA Substance Registry System: 2-((2R,3R,4R)-3,4-Bis-benzyloxy-5-methoxy-2-methyl-tetrahydro-furan-2-yl)-ethanol(887769-08-6)
  • 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: 887769-08-6(Hazardous Substances Data)

887769-08-6 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 887769-08-6 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 8,8,7,7,6 and 9 respectively; the second part has 2 digits, 0 and 8 respectively.
Calculate Digit Verification of CAS Registry Number 887769-08:
(8*8)+(7*8)+(6*7)+(5*7)+(4*6)+(3*9)+(2*0)+(1*8)=256
256 % 10 = 6
So 887769-08-6 is a valid CAS Registry Number.

887769-08-6Downstream Products

887769-08-6Relevant articles and documents

Asymmetric synthesis of the polyol subunit of the macrolide antibiotic, ossamycin

Kutsumura, Noriki,Nishiyama, Shigeru

, p. 5707 - 5709 (2005)

An asymmetric synthesis of the C1-C16 polyol subunit of the macrolide antibiotic, ossamycin, has been achieved through stepwise carbon-chain elongation reaction from D-glucose.

Asymmetric synthesis of the polyol subunit of the macrolide antibiotic, ossamycin: A unique approach utilizing stereochemical specificity

Kutsumura, Noriki,Nishiyama, Shigeru

, p. 468 - 478 (2007/10/03)

An asymmetric synthesis of the C1-C16 polyol subunit 2 of the macrolide antibiotic ossamycin (1) has been achieved through stepwise carbon-chain elongation reaction from D-glucose, based on a chiral pool approach. An outstanding point of this strategy is

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