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141054-98-0

1,6-anhydro-4-O-benzoyl-2,3-dideoxy-β-D-threo-hex-2-enopyranose is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

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  • 141054-98-0 Structure

  • Basic information

    1. Product Name: 1,6-anhydro-4-O-benzoyl-2,3-dideoxy-β-D-threo-hex-2-enopyranose
    2. Synonyms: 1,6-anhydro-4-O-benzoyl-2,3-dideoxy-β-D-threo-hex-2-enopyranose
    3. CAS NO:141054-98-0
    4. Molecular Formula:
    5. Molecular Weight: 232.236
    6. EINECS: N/A
    7. Product Categories: N/A
    8. Mol File: 141054-98-0.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: 1,6-anhydro-4-O-benzoyl-2,3-dideoxy-β-D-threo-hex-2-enopyranose(CAS DataBase Reference)
    10. NIST Chemistry Reference: 1,6-anhydro-4-O-benzoyl-2,3-dideoxy-β-D-threo-hex-2-enopyranose(141054-98-0)
    11. EPA Substance Registry System: 1,6-anhydro-4-O-benzoyl-2,3-dideoxy-β-D-threo-hex-2-enopyranose(141054-98-0)

  • 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: 141054-98-0(Hazardous Substances Data)

141054-98-0 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 141054-98-0 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,4,1,0,5 and 4 respectively; the second part has 2 digits, 9 and 8 respectively.
Calculate Digit Verification of CAS Registry Number 141054-98:
(8*1)+(7*4)+(6*1)+(5*0)+(4*5)+(3*4)+(2*9)+(1*8)=100
100 % 10 = 0
So 141054-98-0 is a valid CAS Registry Number.

141054-98-0Downstream Products

141054-98-0Relevant articles and documents

Synthesis of 1,6-anhydro-2,3-dideoxy-β-D-erythro- and -threo-hex-2-enopyranose from 3,4-di-O-substituted glycals by a facile intramolecular Ferrier reaction

Mereyala,Venkataramanaiah,Dalvoy

, p. 151 - 153 (1992)

The 1,6-anhydro-2,3-dideoxy-β-D-erythro- 7-9 and -threo-hex-2-enopyranoses 10-12 are valuable synthons for the preparation of structurally diverse natural products. This paper reports on a new, general, and efficient route to their synthesis from 3,4-di-O

Clay montmorillonite in carbohydrates : Use of 'claysil' as an efficient heterogenous catalyst for the intramolecular Ferrier reactions leading to 1,6-anhydro rare saccharides

Sharma,Venkata Ramanaiah,Krishnudu

, p. 1905 - 1908 (2007/10/02)

Clay montmorillonite supported silver reagent - claysil - was prepared and advantageously used in the intramolecular Ferrier reaction of 6-hydroxy glycals 1a-9c. The unsaturated sugars 13a-21c so obtained were stereoselectively hydroxylated leading to the

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