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Benzoic acid, 3,5-bis[[3,5-bis[[3,5-bis(dodecyloxy)phenyl]methoxy]phenyl]methoxy]- is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

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  • 852043-03-9 Structure
  • Basic information

    1. Product Name: Benzoic acid, 3,5-bis[[3,5-bis[[3,5-bis(dodecyloxy)phenyl]methoxy]phenyl]methoxy]-
    2. Synonyms:
    3. CAS NO:852043-03-9
    4. Molecular Formula: C145H234O16
    5. Molecular Weight: 2233.44
    6. EINECS: N/A
    7. Product Categories: N/A
    8. Mol File: 852043-03-9.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: Benzoic acid, 3,5-bis[[3,5-bis[[3,5-bis(dodecyloxy)phenyl]methoxy]phenyl]methoxy]-(CAS DataBase Reference)
    10. NIST Chemistry Reference: Benzoic acid, 3,5-bis[[3,5-bis[[3,5-bis(dodecyloxy)phenyl]methoxy]phenyl]methoxy]-(852043-03-9)
    11. EPA Substance Registry System: Benzoic acid, 3,5-bis[[3,5-bis[[3,5-bis(dodecyloxy)phenyl]methoxy]phenyl]methoxy]-(852043-03-9)
  • 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: 852043-03-9(Hazardous Substances Data)

852043-03-9 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 852043-03-9 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 8,5,2,0,4 and 3 respectively; the second part has 2 digits, 0 and 3 respectively.
Calculate Digit Verification of CAS Registry Number 852043-03:
(8*8)+(7*5)+(6*2)+(5*0)+(4*4)+(3*3)+(2*0)+(1*3)=139
139 % 10 = 9
So 852043-03-9 is a valid CAS Registry Number.

852043-03-9Upstream product

852043-03-9Downstream Products

852043-03-9Relevant articles and documents

Effects of polymer architecture and nanoenvironment in acylation reactions employing dendritic (Dialkylamino)pyridine catalysts

Helms, Brett,Liang, Catherine O.,Hawker, Craig J.,Frechet, Jean M. J.

, p. 5411 - 5415 (2005)

The role of architecture and nanoenvironment in the catalytic properties of dendritic polymers containing 4-(dialkylamino)pyridines was investigated in the context of acylation reactions employing sterically demanding tertiary alcohols as substrates. Frechet-type benzyl ether and aliphatic ester dendrimers were prepared in a convergent manner from a common trivalent core containing three DMAP groups while a linear polymer was dendronized with aliphatic esters using a divergent growth scheme. Catalysis experiments clearly indicate that nanoenvironment plays the dominant role in determining the activity of the polymer catalysts, with the polyester platform being superior to the benzyl ether. Polymer architecture played little or no role in affecting catalysis. With respect to molecular transport and catalysis, this represents the first comparative study of the effect of architecture and nanoenvironment using structurally similar dendritic materials.

Self-assembly and liquid-crystalline supramolecular organizations of semifluorinated block co-dendritic supermolecules

Bury, Izabela,Heinrich, Benoit,Bourgogne, Cyril,Mehl, Georg H.,Guillon, Daniel,Donnio, Bertrand

experimental part, p. 452 - 468 (2012/03/22)

The synthesis and self-organizing behaviour into liquid-crystalline mesophases of two libraries of segmented block co-dendrimers are described. The overall structure of the dendritic supermolecules consists of two chemically incompatible molecular moietie

Supramolecular self-organization of "janus-like" diblock codendrimers: Synthesis, thermal behavior, and phase structure modeling

Bury, Izabela,Heinrich, Benoit,Bourgogne, Cyril,Guillon, Daniel,Donnio, Bertrand

, p. 8396 - 8413 (2007/10/03)

We report on the design and synthesis of three series of segmented amphiphilic block codendrimers. and on their self-organizing behavior in liquid-crystalline mesophases. Connecting two prefunctionalized monodendrons, each differing in their chemical cons

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