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183376-76-3

C36H46N4O8S4 is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

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  • 183376-76-3 Structure

  • Basic information

    1. Product Name: C36H46N4O8S4
    2. Synonyms:
    3. CAS NO:183376-76-3
    4. Molecular Formula:
    5. Molecular Weight: 791.047
    6. EINECS: N/A
    7. Product Categories: N/A
    8. Mol File: 183376-76-3.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: C36H46N4O8S4(CAS DataBase Reference)
    10. NIST Chemistry Reference: C36H46N4O8S4(183376-76-3)
    11. EPA Substance Registry System: C36H46N4O8S4(183376-76-3)

  • 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: 183376-76-3(Hazardous Substances Data)

183376-76-3 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 183376-76-3 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,8,3,3,7 and 6 respectively; the second part has 2 digits, 7 and 6 respectively.
Calculate Digit Verification of CAS Registry Number 183376-76:
(8*1)+(7*8)+(6*3)+(5*3)+(4*7)+(3*6)+(2*7)+(1*6)=163
163 % 10 = 3
So 183376-76-3 is a valid CAS Registry Number.

183376-76-3Relevant articles and documents

Thermal removal of BOC-protecting groups during preparation of open-chain polyamines

Krakowiak, Krzysztof E.,Bradshaw, Jerald S.

, p. 3999 - 4004 (2007/10/03)

Per-N-tosylated 3,8-diaza-1,10-decanediamine (9), 4,9-diaza-1,12-dodecanediamine (spermine) (10) and 3,6,9,14,17,20-hexaaza-1,22-docosanediamine (11) were prepared by treating mono-BOC-protected, per-N-tosylated 1,2-ethanediamine (5), 1,3-propanediamine (6) and triethylenetetraamine (7), respectively, with 1,4-dibromobutane and removing the BOC-protecting groups at 100-120°C.

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