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123672-26-4

3,4,5,6-Tetrahydroxy-L-lyxo-hex-1-en is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

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  • 123672-26-4 Structure

  • Basic information

    1. Product Name: 3,4,5,6-Tetrahydroxy-L-lyxo-hex-1-en
    2. Synonyms:
    3. CAS NO:123672-26-4
    4. Molecular Formula:
    5. Molecular Weight: 148.159
    6. EINECS: N/A
    7. Product Categories: N/A
    8. Mol File: 123672-26-4.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: 3,4,5,6-Tetrahydroxy-L-lyxo-hex-1-en(CAS DataBase Reference)
    10. NIST Chemistry Reference: 3,4,5,6-Tetrahydroxy-L-lyxo-hex-1-en(123672-26-4)
    11. EPA Substance Registry System: 3,4,5,6-Tetrahydroxy-L-lyxo-hex-1-en(123672-26-4)

  • 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: 123672-26-4(Hazardous Substances Data)

123672-26-4 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 123672-26-4 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,2,3,6,7 and 2 respectively; the second part has 2 digits, 2 and 6 respectively.
Calculate Digit Verification of CAS Registry Number 123672-26:
(8*1)+(7*2)+(6*3)+(5*6)+(4*7)+(3*2)+(2*2)+(1*6)=114
114 % 10 = 4
So 123672-26-4 is a valid CAS Registry Number.

123672-26-4Relevant articles and documents

Seven-Step Synthesis of All-Nitrogenated Sugar Derivatives Using Sequential Overman Rearrangements

Okuyama, Yuya,Kidena, Mayu,Kato, Erina,Kawano, Sayaka,Ishii, Koki,Maie, Kenta,Miura, Kazuki,Simizu, Siro,Sato, Takaaki,Chida, Noritaka

, p. 5193 - 5198 (2021)

All-nitrogenated sugars (ANSs), in which all hydroxy groups in a carbohydrate are replaced with amino groups, are anticipated to be privileged structures with useful biological activities. However, ANS synthesis has been challenging due to the difficulty in the installation of multi-amino groups. We report herein the development of a concise synthetic route to peracetylated ANSs in seven steps from commercially available monosaccharides. The key to success is the use of the sequential Overman rearrangement, which enables formal simultaneous substitution of four or five hydroxy groups in monosaccharides with amino groups. A variety of ANSs are available through the same reaction sequence starting from different initial monosaccharides by chirality transfer of secondary alcohols. Transformations of the resulting peracetylated ANSs such as glycosylation and deacetylation are also demonstrated. Biological studies reveal that ANS-modified cholesterol show cytotoxicity against human cancer cell lines, whereas each ANS and cholesterol have no cytotoxicity.

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