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CAS

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141514-07-0

4-pentenyl 3,4,6-tri-O-benzoyl-2-benzoyloxyimino-β-D-arabino-hexopyranoside is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

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  • 141514-07-0 Structure

  • Basic information

    1. Product Name: 4-pentenyl 3,4,6-tri-O-benzoyl-2-benzoyloxyimino-β-D-arabino-hexopyranoside
    2. Synonyms:
    3. CAS NO:141514-07-0
    4. Molecular Formula:
    5. Molecular Weight: 677.708
    6. EINECS: N/A
    7. Product Categories: N/A
    8. Mol File: 141514-07-0.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: 4-pentenyl 3,4,6-tri-O-benzoyl-2-benzoyloxyimino-β-D-arabino-hexopyranoside(CAS DataBase Reference)
    10. NIST Chemistry Reference: 4-pentenyl 3,4,6-tri-O-benzoyl-2-benzoyloxyimino-β-D-arabino-hexopyranoside(141514-07-0)
    11. EPA Substance Registry System: 4-pentenyl 3,4,6-tri-O-benzoyl-2-benzoyloxyimino-β-D-arabino-hexopyranoside(141514-07-0)

  • 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: 141514-07-0(Hazardous Substances Data)

141514-07-0 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 141514-07-0 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,4,1,5,1 and 4 respectively; the second part has 2 digits, 0 and 7 respectively.
Calculate Digit Verification of CAS Registry Number 141514-07:
(8*1)+(7*4)+(6*1)+(5*5)+(4*1)+(3*4)+(2*0)+(1*7)=90
90 % 10 = 0
So 141514-07-0 is a valid CAS Registry Number.

141514-07-0Downstream Products

141514-07-0Relevant articles and documents

Various glycosyl donors with a ketone or oxime function next to the anomeric centre: Facile preparation and evaluation of their selectivities in glycosidations

Lichtenthaler,Klares,Lergenmuller,Schwidetzky

, p. 179 - 184 (2007/10/02)

An efficient one-pot procedure is described for the conversion of a variety of hydroxyglycal esters to their 2-oxoglycosyl bromides which simply comprises of brief treatment with nN-bromosuccinimide/methanol at ambient temperature. Exhibiting comparably l

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