Welcome to LookChem.com Sign In|Join Free

CAS

  • or

651718-17-1

2-O-acetyl-3,4,6-tri-O-benzyl-D-mannono-1,5-lactone is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

651718-17-1 Suppliers

Post Buying Request

Recommended suppliersmore

  • Product
  • FOB Price
  • Min.Order
  • Supply Ability
  • Supplier
  • Contact Supplier
  • 651718-17-1 Structure

  • Basic information

    1. Product Name: 2-O-acetyl-3,4,6-tri-O-benzyl-D-mannono-1,5-lactone
    2. Synonyms: 2-O-acetyl-3,4,6-tri-O-benzyl-D-mannono-1,5-lactone
    3. CAS NO:651718-17-1
    4. Molecular Formula:
    5. Molecular Weight: 490.553
    6. EINECS: N/A
    7. Product Categories: N/A
    8. Mol File: 651718-17-1.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: 2-O-acetyl-3,4,6-tri-O-benzyl-D-mannono-1,5-lactone(CAS DataBase Reference)
    10. NIST Chemistry Reference: 2-O-acetyl-3,4,6-tri-O-benzyl-D-mannono-1,5-lactone(651718-17-1)
    11. EPA Substance Registry System: 2-O-acetyl-3,4,6-tri-O-benzyl-D-mannono-1,5-lactone(651718-17-1)

  • 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: 651718-17-1(Hazardous Substances Data)

651718-17-1 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 651718-17-1 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 6,5,1,7,1 and 8 respectively; the second part has 2 digits, 1 and 7 respectively.
Calculate Digit Verification of CAS Registry Number 651718-17:
(8*6)+(7*5)+(6*1)+(5*7)+(4*1)+(3*8)+(2*1)+(1*7)=161
161 % 10 = 1
So 651718-17-1 is a valid CAS Registry Number.

651718-17-1Relevant articles and documents

Expedient and versatile formation of novel amino-deoxy-ketoheptuloses

Leshch, Yevgeniy,Jacobsen, Anna,Thimm, Julian,Thiem, Joachim

supporting information, p. 4948 - 4951 (2013/10/22)

Novel monoketoheptuloses have been synthesized employing an amination step in a pre- and/or post-C1 chain elongation using a Petasis reagent by starting from aldohexoses or aldohexosamines. A series of gluco and manno configured 1-/3-deoxy-1-/3-amino-keto

Stereoselective synthesis of allyl-C-mannosyl compounds: Use of a temporary silicon connection in intramolecular allylation strategies with allylsilanes

Beignet, Julien,Tiernan, James,Woo, Chang H.,Kariuki, Benson M.,Cox, Liam R.

, p. 6341 - 6356 (2007/10/03)

Methyl mannoside 16 containing an allyldimethylsilyl ether at C(2) was synthesized in nine steps from D-mannose. Reaction with TMSOTf in MeCN at room-temperature effected C-glycosylation to provide the α-allyl-C- mannosyl product 18 with excellent stereos

Synthesis of monosaccharide-derived spirocyclic cyclopropylamines and their evaluation as glycosidase inhibitors

Bluechel, Christian,Ramana, Chepuri Venkata,Vasella, Andrea

, p. 2998 - 3036 (2007/10/03)

The glucose-, mannose-, and galactose-derived spirocyclic cyclopropylammonium chlorides 1a - 1d, 2a - 2d and 3a-3d were prepared as potential glycosidase inhibitors. Cyclopropanation of the diazirine 5 with ethyl acrylate led in 71% yield to a 4:5:1:20 mi

Post a RFQ

Enter 15 to 2000 letters.Word count: 0 letters

Attach files(File Format: Jpeg, Jpg, Gif, Png, PDF, PPT, Zip, Rar,Word or Excel Maximum File Size: 3MB)

1

What can I do for you?
Get Best Price

Get Best Price for 651718-17-1