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  • 1422182-25-9 Structure
  • Basic information

    1. Product Name: C60H66O12
    2. Synonyms:
    3. CAS NO:1422182-25-9
    4. Molecular Formula:
    5. Molecular Weight: 979.177
    6. EINECS: N/A
    7. Product Categories: N/A
    8. Mol File: 1422182-25-9.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: C60H66O12(CAS DataBase Reference)
    10. NIST Chemistry Reference: C60H66O12(1422182-25-9)
    11. EPA Substance Registry System: C60H66O12(1422182-25-9)
  • 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: 1422182-25-9(Hazardous Substances Data)

1422182-25-9 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 1422182-25-9 includes 10 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 7 digits, 1,4,2,2,1,8 and 2 respectively; the second part has 2 digits, 2 and 5 respectively.
Calculate Digit Verification of CAS Registry Number 1422182-25:
(9*1)+(8*4)+(7*2)+(6*2)+(5*1)+(4*8)+(3*2)+(2*2)+(1*5)=119
119 % 10 = 9
So 1422182-25-9 is a valid CAS Registry Number.

1422182-25-9Downstream Products

1422182-25-9Relevant articles and documents

Role of hydrogen bonding on the self-organization of phenyleneethynylenes on surfaces

Zalake, Pratap,Thomas, K. George

, p. 2242 - 2249 (2013/03/29)

A series of carboxylic acid substituted phenyleneethynylenes, having a rigid backbone of 2.7 ± 0.1 nm, were synthesized by following the Heck-Cassar-Sonagashira-Hagihara cross-coupling reaction. Hydrogen bonding, through the formation of cyclic dimers of carboxylic acid, is more preferred over catemeric structures in all the molecular systems under investigation. The formation of extended two-dimensional patterns on highly oriented pyrolitic graphite (HOPG) surface is dictated by the position as well as number of the carboxylic acid groups on the phenyleneethynylenes. Highly ordered extended arrangements, in the linear and stepwise fashion, were observed when the carboxylic acid groups are attached in the para and meta positions of phenyleneethynylenes. The vital role of the number of carboxylic acid on the organization of molecules is evident in the case of tetracarboxylic acid derivative wherein a Kagome-type structure was observed. Further, the coassembly of two types of phenyleneethynylenes was achieved on HOPG surface through acid base interaction.

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