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5-acetamido-9-O-benzoyl-3,5-dideoxy-D-glycero-β-D-galacto-2-nonulopyranosonic acid is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

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  • 114857-63-5 Structure
  • Basic information

    1. Product Name: 5-acetamido-9-O-benzoyl-3,5-dideoxy-D-glycero-β-D-galacto-2-nonulopyranosonic acid
    2. Synonyms: 5-acetamido-9-O-benzoyl-3,5-dideoxy-D-glycero-β-D-galacto-2-nonulopyranosonic acid
    3. CAS NO:114857-63-5
    4. Molecular Formula:
    5. Molecular Weight: 413.381
    6. EINECS: N/A
    7. Product Categories: N/A
    8. Mol File: 114857-63-5.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-acetamido-9-O-benzoyl-3,5-dideoxy-D-glycero-β-D-galacto-2-nonulopyranosonic acid(CAS DataBase Reference)
    10. NIST Chemistry Reference: 5-acetamido-9-O-benzoyl-3,5-dideoxy-D-glycero-β-D-galacto-2-nonulopyranosonic acid(114857-63-5)
    11. EPA Substance Registry System: 5-acetamido-9-O-benzoyl-3,5-dideoxy-D-glycero-β-D-galacto-2-nonulopyranosonic acid(114857-63-5)
  • 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: 114857-63-5(Hazardous Substances Data)

114857-63-5 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 114857-63-5 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,1,4,8,5 and 7 respectively; the second part has 2 digits, 6 and 3 respectively.
Calculate Digit Verification of CAS Registry Number 114857-63:
(8*1)+(7*1)+(6*4)+(5*8)+(4*5)+(3*7)+(2*6)+(1*3)=135
135 % 10 = 5
So 114857-63-5 is a valid CAS Registry Number.

114857-63-5Downstream Products

114857-63-5Relevant articles and documents

Synthesis and evaluation of C-9 modified N-acetylneuraminic acid derivatives as substrates for N-acetylneuraminic acid aldolase

Kiefel, Milton J.,Wilson, Jennifer C.,Bennett, Simon,Gredley, Matt,Von Itzstein, Mark

, p. 657 - 664 (2007/10/03)

Several C-9 modified N-acetylneuraminic acid derivatives have been synthesised and evaluated as substrates of N-acetylneuraminic acid aldolase. Simple C-9 acyl or ether modified derivatives of N-acetylneuraminic acid were found to be accepted as substrates by the enzyme, albeit being transformed more slowly than Neu5Ac itself. 1H NMR spectroscopy was used to evaluate the extent of the enzyme catalysed transformation of these compounds. Interestingly, the chain-extended Neu5Ac derivative 16 is not a substrate for N-acetylneuraminate lyase and behaves as an inhibitor of the enzyme. Copyright (C) 2000 Elsevier Science Ltd.

SYNTHESIS OF 9-O-ACYL- AND 4-O-ACETYL-SIALIC ACIDS

Ogura, Haruo,Furuhata, Kimio,Sato, Shingo,Anazawa, Katsuko,Itoh, Masayoshi,Shitori, Yoshiyasu

, p. 77 - 86 (2007/10/02)

Various 9-O-acyl derivatives of N-acetyl- and N-glycoloyl-neuraminic acid, and O-(5-acetamido-3,5-dideoxy-D-glycero-α- and β-D-galacto-2-nonulopyranosylonic acid)-(2->6)-O-β-D-galactopyranosyl-(1->4)-D-glucopyranose were regioselectively synthesized by us

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