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179927-64-1

5-O-benzyl-2-deoxy-2-fluoro-D-γ-xylonic lactone is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

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  • 179927-64-1 Structure

  • Basic information

    1. Product Name: 5-O-benzyl-2-deoxy-2-fluoro-D-γ-xylonic lactone
    2. Synonyms: 5-O-benzyl-2-deoxy-2-fluoro-D-γ-xylonic lactone
    3. CAS NO:179927-64-1
    4. Molecular Formula:
    5. Molecular Weight: 240.231
    6. EINECS: N/A
    7. Product Categories: N/A
    8. Mol File: 179927-64-1.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: 5-O-benzyl-2-deoxy-2-fluoro-D-γ-xylonic lactone(CAS DataBase Reference)
    10. NIST Chemistry Reference: 5-O-benzyl-2-deoxy-2-fluoro-D-γ-xylonic lactone(179927-64-1)
    11. EPA Substance Registry System: 5-O-benzyl-2-deoxy-2-fluoro-D-γ-xylonic lactone(179927-64-1)

  • 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: 179927-64-1(Hazardous Substances Data)

179927-64-1 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 179927-64-1 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,7,9,9,2 and 7 respectively; the second part has 2 digits, 6 and 4 respectively.
Calculate Digit Verification of CAS Registry Number 179927-64:
(8*1)+(7*7)+(6*9)+(5*9)+(4*2)+(3*7)+(2*6)+(1*4)=201
201 % 10 = 1
So 179927-64-1 is a valid CAS Registry Number.

179927-64-1Downstream Products

179927-64-1Relevant articles and documents

Asymmetric synthesis of 2-deoxy-2-fluoro-γ-aldonolactones and their conversion to 2-deoxy-2-fluoropentoses

Davis, Franklin A.,Qi, Hongyan

, p. 4345 - 4348 (1996)

2-Fluoro-2-deoxy-γ-xylonic and -lyxonic lactones, 7a and 7b, were prepared via the diastereoselective fluorination of the α,β-unsaturated chiral imide 5 followed by dihydroxylation. Lactones 7a and 7b were converted to 2-deoxy-2-fluoro-xylo-D-pyranose (1) and 2-deoxy-2-fluoro-lyxo-L-pyranose (2) by reduction and deprotection.

Application of oxazolidinone α-fluoro amide chiral building blocks in the asymmetric synthesis of fluorinated carbohydrates: 2-Deoxy-2-fluoropentoses

Davis, Franklin A.,Qi, Hongyan,Sundarababu, Gajendran

, p. 5303 - 5310 (2007/10/03)

Deconjugative electrophilic fluorination of the lithium dienolate of Z-α,β-unsaturated imide (+)-9 with N-fluorobenzene-sulfonimide (NFSi) afforded the E-β,γ-unsaturated α-fluoro imide (+)-10 as a single diastereoisomer. Dihydroxylation resulted in the formation of 2-fluoro-2-deoxy-γ-xylonic and -lyxonic lactones, 12a and 12b, respectively. Reduction and deprotection of the lactones afforded 2-deoxy-2-fluoro-xylo-D-pyranose (15) and 2-deoxy-2-fluoro-lyxo-L-pyranose (17). (C) 2000 Elsevier Science Ltd.

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