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Benzamide, 4-[(4S)-2,2-dioxido-4-phenyl-1,2,3-oxathiazolidin-3-yl]-N-propyl- is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

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  • 876747-69-2 Structure
  • Basic information

    1. Product Name: Benzamide, 4-[(4S)-2,2-dioxido-4-phenyl-1,2,3-oxathiazolidin-3-yl]-N-propyl-
    2. Synonyms:
    3. CAS NO:876747-69-2
    4. Molecular Formula: C18H20N2O4S
    5. Molecular Weight: 360.434
    6. EINECS: N/A
    7. Product Categories: N/A
    8. Mol File: 876747-69-2.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: Benzamide, 4-[(4S)-2,2-dioxido-4-phenyl-1,2,3-oxathiazolidin-3-yl]-N-propyl-(CAS DataBase Reference)
    10. NIST Chemistry Reference: Benzamide, 4-[(4S)-2,2-dioxido-4-phenyl-1,2,3-oxathiazolidin-3-yl]-N-propyl-(876747-69-2)
    11. EPA Substance Registry System: Benzamide, 4-[(4S)-2,2-dioxido-4-phenyl-1,2,3-oxathiazolidin-3-yl]-N-propyl-(876747-69-2)
  • 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: 876747-69-2(Hazardous Substances Data)

876747-69-2 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 876747-69-2 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 8,7,6,7,4 and 7 respectively; the second part has 2 digits, 6 and 9 respectively.
Calculate Digit Verification of CAS Registry Number 876747-69:
(8*8)+(7*7)+(6*6)+(5*7)+(4*4)+(3*7)+(2*6)+(1*9)=242
242 % 10 = 2
So 876747-69-2 is a valid CAS Registry Number.

876747-69-2Downstream Products

876747-69-2Relevant articles and documents

Cu-catalyzed N-arylation of oxazolidinones: An efficient synthesis of the κ-opioid receptor agonist CJ-15161

Ghosh, Arun,Sieser, Janice E.,Caron, Stephane,Couturier, Michel,Dupont-Gaudet, Kristina,Girardin, Melina

, p. 1258 - 1261 (2007/10/03)

An efficient method for intermolecular N-arylation of oxazolidinones using catalytic copper in the presence of a bidentate ligand is reported. The conditions allow the use of copper and can be used to prepare enantiopure N-aryl β-amino alcohols. A short,

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