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852054-09-2

Carbamic acid, [[4-(3,3,4,4,5,5,6,6,6-nonafluorohexyl)phenyl]methyl]propyl-, 1,1-dimethylethyl ester is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

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  • 852054-09-2 Structure

  • Basic information

    1. Product Name: Carbamic acid, [[4-(3,3,4,4,5,5,6,6,6-nonafluorohexyl)phenyl]methyl]propyl-, 1,1-dimethylethyl ester
    2. Synonyms:
    3. CAS NO:852054-09-2
    4. Molecular Formula: C21H26F9NO2
    5. Molecular Weight: 495.429
    6. EINECS: N/A
    7. Product Categories: N/A
    8. Mol File: 852054-09-2.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: Carbamic acid, [[4-(3,3,4,4,5,5,6,6,6-nonafluorohexyl)phenyl]methyl]propyl-, 1,1-dimethylethyl ester(CAS DataBase Reference)
    10. NIST Chemistry Reference: Carbamic acid, [[4-(3,3,4,4,5,5,6,6,6-nonafluorohexyl)phenyl]methyl]propyl-, 1,1-dimethylethyl ester(852054-09-2)
    11. EPA Substance Registry System: Carbamic acid, [[4-(3,3,4,4,5,5,6,6,6-nonafluorohexyl)phenyl]methyl]propyl-, 1,1-dimethylethyl ester(852054-09-2)

  • 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: 852054-09-2(Hazardous Substances Data)

852054-09-2 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 852054-09-2 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 8,5,2,0,5 and 4 respectively; the second part has 2 digits, 0 and 9 respectively.
Calculate Digit Verification of CAS Registry Number 852054-09:
(8*8)+(7*5)+(6*2)+(5*0)+(4*5)+(3*4)+(2*0)+(1*9)=152
152 % 10 = 2
So 852054-09-2 is a valid CAS Registry Number.

852054-09-2Relevant articles and documents

Preparative fluorous mixture synthesis of diazonium-functionalized oligo(phenylene vinylene)s

Jian, Huahua,Tour, James M.

, p. 3396 - 3424 (2007/10/03)

(Chemical Equation Presented) A series of building blocks for the synthesis of oligo(phenylene vinylene)s (OPVs) and hybrid oligomers were prepared, and alternating Heck coupling and Horner-Wadswoth-Emmons (HWE) reactions were used to couple the building blocks. Model studies were carried out to optimize the reaction strategies. The products were made to bear aryl diazonium functionalities that allow them to be used as surface grafting moieties in hybrid silicon/molecule assemblies. A library of OPV and hybrid oligomer tetramers was synthesized using fluorous mixture synthesis (FMS). The fluorous tags, which are secondary amines bearing different numbers of fluorine atoms, were synthesized and used as phase tags in mixture synthesis. The tags and substrates were anchored together by triazene linkages. The mixture synthesis was monitored by analytical HPLC on a fluorous column, and isolation of final OPV and hybrid oligomer tetramers was achieved by preparative HPLC. At the end of the FMS, after demixing, the tagged products were detagged by cleaving the triazene linkage and generating a series of aryl diazonium compounds. The fluorous tags could be recovered and reused. The NMR spectra of the 1-aryl-3,3-dialkyltriazenes are discussed.

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