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114467-03-7

C14H13N2O5S*H(1+) is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

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  • 114467-03-7 Structure

  • Basic information

    1. Product Name: C14H13N2O5S*H(1+)
    2. Synonyms: C14H13N2O5S*H(1+)
    3. CAS NO:114467-03-7
    4. Molecular Formula:
    5. Molecular Weight: 322.342
    6. EINECS: N/A
    7. Product Categories: N/A
    8. Mol File: 114467-03-7.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: C14H13N2O5S*H(1+)(CAS DataBase Reference)
    10. NIST Chemistry Reference: C14H13N2O5S*H(1+)(114467-03-7)
    11. EPA Substance Registry System: C14H13N2O5S*H(1+)(114467-03-7)

  • 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: 114467-03-7(Hazardous Substances Data)

114467-03-7 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 114467-03-7 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,1,4,4,6 and 7 respectively; the second part has 2 digits, 0 and 3 respectively.
Calculate Digit Verification of CAS Registry Number 114467-03:
(8*1)+(7*1)+(6*4)+(5*4)+(4*6)+(3*7)+(2*0)+(1*3)=107
107 % 10 = 7
So 114467-03-7 is a valid CAS Registry Number.

114467-03-7Relevant articles and documents

Structural Effects on the Transition States of Imine-Forming Eliminations in N-Substituted O-(Arylsulfonyl)hydroxylamines

Hoffman, Robert V.,Shankweiler, Jean M.

, p. 4019 - 4022 (2007/10/02)

A series of amines with various alkyl and aryl substituents at C-1 were converted to the corresponding N-(arylsulfonoxy)amines, which served as precursors for base-promoted, imine-forming elimination.By varying the bases used to promote the elimination and by varying the leaving groups attached to nitrogen, the Broensted parameters β and βlgCH3 were determined.These were used to locate the transition state on the More O'Ferrall-Jencks energy surface for elimination.Substituents were found to influence the structure of the activated complex markedly.Resonance effects were most important, while inductive effects had little influence .

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