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114916-04-0

N1,N5-di-(E)-coumaroyl-spermidine is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

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  • 114916-04-0 Structure

  • Basic information

    1. Product Name: N1,N5-di-(E)-coumaroyl-spermidine
    2. Synonyms: N1,N5-di-(E)-coumaroyl-spermidine
    3. CAS NO:114916-04-0
    4. Molecular Formula:
    5. Molecular Weight: 437.539
    6. EINECS: N/A
    7. Product Categories: N/A
    8. Mol File: 114916-04-0.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: N1,N5-di-(E)-coumaroyl-spermidine(CAS DataBase Reference)
    10. NIST Chemistry Reference: N1,N5-di-(E)-coumaroyl-spermidine(114916-04-0)
    11. EPA Substance Registry System: N1,N5-di-(E)-coumaroyl-spermidine(114916-04-0)

  • 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: 114916-04-0(Hazardous Substances Data)

114916-04-0 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 114916-04-0 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,1,4,9,1 and 6 respectively; the second part has 2 digits, 0 and 4 respectively.
Calculate Digit Verification of CAS Registry Number 114916-04:
(8*1)+(7*1)+(6*4)+(5*9)+(4*1)+(3*6)+(2*0)+(1*4)=110
110 % 10 = 0
So 114916-04-0 is a valid CAS Registry Number.

114916-04-0Relevant articles and documents

Synthesis of 13C-dilabeled 4-coumaroylspermidines

Geneste, Herve,Hesse, Manfred

, p. 15199 - 15214 (2007/10/03)

Five 13C-dilabeled constitution isomers of 4-coumaroylspermidines were prepared in nine to eleven steps: N1,4-di[(E)-4-coumaroyl]-(5,8- 13C2)spermidine (13b), N1-[(E)-4-coumaroyl]-(5,8-13C2)spermidine (17b), N1,8-di[(E)-4-coumaroyl]-(1,4-13C2)spermidine (20b), N4-[(E)-4- coumaroyl]-(1,4-13C2)spermidine (24b) and N1,4,8-tri[(E)-4-coumaroyl]- (5,8-13C2)spermidine (26). The two 13C-atoms were subsequently introduced using labeled potassium cyanide. The synthesis proceeds through stepwise construction of the polyamine backbone including protection and deprotection steps of the amino functions. Based on 1H-1H NOE interactions, the preliminary study of their binding reveals that 20b binds to tRNA in the same way as spermidine does, whereas 24b and 26 do not show any NOE effects with the tRNA protons.

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