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156769-29-8

1-O-acetyl-2,3,4-tri-O-benzyl-α-D-fucopyranose is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

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  • 156769-29-8 Structure

  • Basic information

    1. Product Name: 1-O-acetyl-2,3,4-tri-O-benzyl-α-D-fucopyranose
    2. Synonyms: 1-O-acetyl-2,3,4-tri-O-benzyl-α-D-fucopyranose
    3. CAS NO:156769-29-8
    4. Molecular Formula:
    5. Molecular Weight: 476.569
    6. EINECS: N/A
    7. Product Categories: N/A
    8. Mol File: 156769-29-8.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: 1-O-acetyl-2,3,4-tri-O-benzyl-α-D-fucopyranose(CAS DataBase Reference)
    10. NIST Chemistry Reference: 1-O-acetyl-2,3,4-tri-O-benzyl-α-D-fucopyranose(156769-29-8)
    11. EPA Substance Registry System: 1-O-acetyl-2,3,4-tri-O-benzyl-α-D-fucopyranose(156769-29-8)

  • 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: 156769-29-8(Hazardous Substances Data)

156769-29-8 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 156769-29-8 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,5,6,7,6 and 9 respectively; the second part has 2 digits, 2 and 9 respectively.
Calculate Digit Verification of CAS Registry Number 156769-29:
(8*1)+(7*5)+(6*6)+(5*7)+(4*6)+(3*9)+(2*2)+(1*9)=178
178 % 10 = 8
So 156769-29-8 is a valid CAS Registry Number.

156769-29-8Downstream Products

156769-29-8Relevant articles and documents

The structural revision and total synthesis of carambolaflavone a

Wang, Yong,Liu, Miao,Liu, Lei,Xia, Jian-Hui,Du, Yu-Guo,Sun, Jian-Song

, p. 4111 - 4118 (2018)

The synthesis of both enantiomers of carambolaflavone A, the antidiabetic and flavonoid C-glycoside, was achieved for the first time via a 12-longest-linear-step with 16% (l-fucose) and 11% (d-fucose) overall yields. Through the synthetic investigation, the adverse effect of 4A MS in Suzuki C-glycosylation was disclosed, the mechanism of hydrogen-bonded-phenol involved Suzuki C-glycosylation was clarified, and the authentic structure of carambolaflavone A was also determined.

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