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1206703-13-0

C18H31N5O2 is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

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  • 1206703-13-0 Structure

  • Basic information

    1. Product Name: C18H31N5O2
    2. Synonyms: C18H31N5O2
    3. CAS NO:1206703-13-0
    4. Molecular Formula:
    5. Molecular Weight: 349.476
    6. EINECS: N/A
    7. Product Categories: N/A
    8. Mol File: 1206703-13-0.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: C18H31N5O2(CAS DataBase Reference)
    10. NIST Chemistry Reference: C18H31N5O2(1206703-13-0)
    11. EPA Substance Registry System: C18H31N5O2(1206703-13-0)

  • 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: 1206703-13-0(Hazardous Substances Data)

1206703-13-0 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 1206703-13-0 includes 10 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 7 digits, 1,2,0,6,7,0 and 3 respectively; the second part has 2 digits, 1 and 3 respectively.
Calculate Digit Verification of CAS Registry Number 1206703-13:
(9*1)+(8*2)+(7*0)+(6*6)+(5*7)+(4*0)+(3*3)+(2*1)+(1*3)=110
110 % 10 = 0
So 1206703-13-0 is a valid CAS Registry Number.

1206703-13-0Relevant articles and documents

Synthesis of novel polymer/urea peptoid conjugates using RAFT polymerization

Chen, Xiaoping,Ayres, Neil

, p. 1341 - 1348 (2011/10/01)

The synthesis of novel urea peptoids and their conjugation to polymers prepared using reversible addition-fragmentation chain transfer (RAFT) polymerization is reported. Statistical copolymers of poly(styrene-co-3- azidopropyl methacrylate) (poly(styrene-co-AzPMA)) and poly(3-O-methacryloyl1, 2: 5, 6-di-O-isopropylidene-D-glucofuranose-co-AzPMA) (poly(MAIpGlc-co-AzPMA)) were synthesized with high molecular weight and narrow molecular weight distributions. The polymer conjugates were formed using copper-catalyzed azide/alkyne cycloaddition chemistry and confirmed by FTIR and 1H NMR spectroscopy. Following conjugate formation with poly(MAIpGlc-co-AzPMA) and the urea peptoid the isopropylidene groups were removed using dilute trifluoroacetic acid. This yielded a sugar functionalized water-soluble, polymer/urea peptoid conjugate. Reactions with fluorescent compounds demonstrated that the peptoids can be further modified after conjugation to the polymer.

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