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CAS

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75161-24-9

N-Benzylidenamino-thiomorpholin is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

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  • 75161-24-9 Structure

  • Basic information

    1. Product Name: N-Benzylidenamino-thiomorpholin
    2. Synonyms: N-Benzylidenamino-thiomorpholin
    3. CAS NO:75161-24-9
    4. Molecular Formula:
    5. Molecular Weight: 206.312
    6. EINECS: N/A
    7. Product Categories: N/A
    8. Mol File: 75161-24-9.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: N-Benzylidenamino-thiomorpholin(CAS DataBase Reference)
    10. NIST Chemistry Reference: N-Benzylidenamino-thiomorpholin(75161-24-9)
    11. EPA Substance Registry System: N-Benzylidenamino-thiomorpholin(75161-24-9)

  • 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: 75161-24-9(Hazardous Substances Data)

75161-24-9 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 75161-24-9 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 7,5,1,6 and 1 respectively; the second part has 2 digits, 2 and 4 respectively.
Calculate Digit Verification of CAS Registry Number 75161-24:
(7*7)+(6*5)+(5*1)+(4*6)+(3*1)+(2*2)+(1*4)=119
119 % 10 = 9
So 75161-24-9 is a valid CAS Registry Number.

75161-24-9Downstream Products

75161-24-9Relevant articles and documents

On the Reactivity of Thiomorpholine and Alkyl Substituted Thiomorpholines 4. (On the Joint Action of Elementary Sulfur and Gaseous Ammonia on Ketones, 94.)

Asinger, Friedrich,Saus, Alfons,Wachtendonk, Magdalena von

, p. 385 - 398 (2007/10/02)

Thiomorpholine as well as alkyl substituted thiomorpholines and their S-dioxides, respectively, are transformed into the corresponding N-Aminothiomorpholines by nitrosation (1-5) followed by the reduction with zinc in acetic acid/acetic acid anhydride und

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