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1,1,3,3-tetramethyl-2-phenyl-isouronium cation is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

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  • 31433-02-0 Structure
  • Basic information

    1. Product Name: 1,1,3,3-tetramethyl-2-phenyl-isouronium cation
    2. Synonyms:
    3. CAS NO:31433-02-0
    4. Molecular Formula:
    5. Molecular Weight: 193.269
    6. EINECS: N/A
    7. Product Categories: N/A
    8. Mol File: 31433-02-0.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: 1,1,3,3-tetramethyl-2-phenyl-isouronium cation(CAS DataBase Reference)
    10. NIST Chemistry Reference: 1,1,3,3-tetramethyl-2-phenyl-isouronium cation(31433-02-0)
    11. EPA Substance Registry System: 1,1,3,3-tetramethyl-2-phenyl-isouronium cation(31433-02-0)
  • 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: 31433-02-0(Hazardous Substances Data)

31433-02-0 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 31433-02-0 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 3,1,4,3 and 3 respectively; the second part has 2 digits, 0 and 2 respectively.
Calculate Digit Verification of CAS Registry Number 31433-02:
(7*3)+(6*1)+(5*4)+(4*3)+(3*3)+(2*0)+(1*2)=70
70 % 10 = 0
So 31433-02-0 is a valid CAS Registry Number.

31433-02-0Downstream Products

31433-02-0Relevant articles and documents

Unveiling and tackling guanidinium peptide coupling reagent side reactions towards the development of peptide-drug conjugates

Vrettos, Eirinaios I.,Sayyad, Nisar,Mavrogiannaki, Eftychia M.,Stylos, Evgenios,Kostagianni, Androniki D.,Papas, Serafim,Mavromoustakos, Thomas,Theodorou, Vassiliki,Tzakos, Andreas G.

, p. 50519 - 50526 (2017)

Peptide coupling reagents and especially uronium/guanidinium salts have been extensively utilized in solid-phase peptide synthesis. However, the impact of these reagents in solution phase synthesis, normally used in the formation of peptide-drug conjugates (PDCs), has not been fully explored. Herein, we identified that when guanidinium salts are used in classical peptide coupling conditions, besides leading to the formation of amide bonds, a uronium derivative can also be installed on specific amino acid scaffolds. The formation of this side product depends on the reaction conditions, as also on the nucleophilicity of the susceptible groups. Conditions to avoid this side product formation and a putative reaction mechanism describing its formation are reported.

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