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1008103-33-0

C25H33N3O5S is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

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  • 1008103-33-0 Structure

  • Basic information

    1. Product Name: C25H33N3O5S
    2. Synonyms:
    3. CAS NO:1008103-33-0
    4. Molecular Formula:
    5. Molecular Weight: 487.62
    6. EINECS: N/A
    7. Product Categories: N/A
    8. Mol File: 1008103-33-0.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: C25H33N3O5S(CAS DataBase Reference)
    10. NIST Chemistry Reference: C25H33N3O5S(1008103-33-0)
    11. EPA Substance Registry System: C25H33N3O5S(1008103-33-0)

  • 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: 1008103-33-0(Hazardous Substances Data)

1008103-33-0 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 1008103-33-0 includes 10 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 7 digits, 1,0,0,8,1,0 and 3 respectively; the second part has 2 digits, 3 and 3 respectively.
Calculate Digit Verification of CAS Registry Number 1008103-33:
(9*1)+(8*0)+(7*0)+(6*8)+(5*1)+(4*0)+(3*3)+(2*3)+(1*3)=80
80 % 10 = 0
So 1008103-33-0 is a valid CAS Registry Number.

1008103-33-0Relevant articles and documents

Multicomponent Synthesis of Novel 2- and 3-Substituted Dihydrobenzo[1,4]oxazepinones and Tetrahydrobenzo[1,4]diazepin-5-ones and their Conformational Analysis

Banfi, Luca,Basso, Andrea,Guanti, Giuseppe,Lecinska, Paulina,Riva, Renata,Rocca, Valeria

experimental part, p. 699 - 728 (2009/09/25)

By coupling an Ugi multicomponent condensation with a Mitsunobu reaction, a series of 2- and 3-substituted dihydrobenzo[1,4]oxazepinones and tetrahydrobenzo[1,4]diazepin-5-ones was synthesized in a very convergent manner. The strategy involves the use of substituted ethanolamines as amino components and of salicylic or N-methanesulphonyl anthranilic acid as carboxylic component. The general scope has been evaluated; in some cases better results have been obtained by reverting the order of the two reactions. A thorough conformational analysis on these products has been carried out through NMR, showing that in most cases a single conformation was strongly favoured.

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