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  • 1028436-90-9 Structure
  • Basic information

    1. Product Name: C34H38N4O5S
    2. Synonyms: C34H38N4O5S
    3. CAS NO:1028436-90-9
    4. Molecular Formula:
    5. Molecular Weight: 614.766
    6. EINECS: N/A
    7. Product Categories: N/A
    8. Mol File: 1028436-90-9.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: C34H38N4O5S(CAS DataBase Reference)
    10. NIST Chemistry Reference: C34H38N4O5S(1028436-90-9)
    11. EPA Substance Registry System: C34H38N4O5S(1028436-90-9)
  • 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: 1028436-90-9(Hazardous Substances Data)

1028436-90-9 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 1028436-90-9 includes 10 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 7 digits, 1,0,2,8,4,3 and 6 respectively; the second part has 2 digits, 9 and 0 respectively.
Calculate Digit Verification of CAS Registry Number 1028436-90:
(9*1)+(8*0)+(7*2)+(6*8)+(5*4)+(4*3)+(3*6)+(2*9)+(1*0)=139
139 % 10 = 9
So 1028436-90-9 is a valid CAS Registry Number.

1028436-90-9Downstream Products

1028436-90-9Relevant articles and documents

Role of benzimidazole (Bid) in the δ-opioid agonist pseudopeptide H-Dmt-Tic-NH-CH2-Bid (UFP-502)

Salvadori, Severo,Fiorini, Stella,Trapella, Claudio,Porreca, Frank,Davis, Peg,Sasaki, Yusuke,Ambo, Akihiro,Marczak, Ewa D.,Lazarus, Lawrence H.,Balboni, Gianfranco

, p. 3032 - 3038 (2008/09/19)

H-Dmt-Tic-NH-CH2-Bid (UFP-502) was the first δ-opioid agonist prepared from the Dmt-Tic pharmacophore. It showed interesting pharmacological properties, such as stimulation of mRNA BDNF expression and antidepression. To evaluate the importance of 1H-benzimidazol-2-yl (Bid) in the induction of δ-agonism, it was substituted by similar heterocycles: The substitution of NH(1) by O or S transforms the reference δ-agonist into δ-antagonists. Phenyl ring of benzimidazole is not important for δ-agonism; in fact 1H-imidazole-2-yl retains δ-agonist activity.

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