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PARA-DODECYLCALIX(8)ARENE is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

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  • 102622-20-8 Structure
  • Basic information

    1. Product Name: PARA-DODECYLCALIX(8)ARENE
    2. Synonyms: PARA-DODECYLCALIX(8)ARENE
    3. CAS NO:102622-20-8
    4. Molecular Formula: C152H240 O8
    5. Molecular Weight: 2195.53
    6. EINECS: N/A
    7. Product Categories: N/A
    8. Mol File: 102622-20-8.mol
  • Chemical Properties

    1. Melting Point: N/A
    2. Boiling Point: N/A
    3. Flash Point: N/A
    4. Appearance: /
    5. Density: N/A
    6. Refractive Index: N/A
    7. Storage Temp.: N/A
    8. Solubility: N/A
    9. CAS DataBase Reference: PARA-DODECYLCALIX(8)ARENE(CAS DataBase Reference)
    10. NIST Chemistry Reference: PARA-DODECYLCALIX(8)ARENE(102622-20-8)
    11. EPA Substance Registry System: PARA-DODECYLCALIX(8)ARENE(102622-20-8)
  • 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: 102622-20-8(Hazardous Substances Data)

102622-20-8 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 102622-20-8 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,0,2,6,2 and 2 respectively; the second part has 2 digits, 2 and 0 respectively.
Calculate Digit Verification of CAS Registry Number 102622-20:
(8*1)+(7*0)+(6*2)+(5*6)+(4*2)+(3*2)+(2*2)+(1*0)=68
68 % 10 = 8
So 102622-20-8 is a valid CAS Registry Number.

102622-20-8Downstream Products

102622-20-8Relevant articles and documents

PREPARATION OF SERIES OF CALIX(6)ARENES AND CALIX(8)ARENES DERIVED FROM P-N-ALKYKPHENOLS.

Asfari, Z.,Vicens, J.

, p. 2659 - 2660 (1988)

The preparation of series of p-n-alkylcalix(6)arenes and p-n-alkylcalix(8)arenes by p-n-alkylphenol-formaldehyde condensations in basic conditions is described.

METAL COMPOUNDS OF CALIXARENES, DETERGENT COMPOSITIONS CONTAINING THEM AND USE THEREOF IN LUBRICANT COMPOSITIONS

-

Paragraph 0322; 0323; 0324; 0325, (2018/09/12)

The present invention relates to a metal compound of calixarene not containing sulfur and dispersible in oil, which can be partially salified, or neutral, or basic or overbased, said calixarene having general formula (I) in which: a) R1, R2, R3 and R4 are independently selected from hydrogen, or a group containing carbon and hydrogen, or a group containing in addition to carbon and hydrogen also heteroatoms, provided that said heteroatoms are not sulfur; b) one of the two substituents R5 and R6 is hydrogen, while the other may be selected from hydrogen, or a linear or branched alkyl with a number of carbon atoms between 1 and 6, preferably methyl, ethyl, 1-propyl, 2-propyl, n-butyl, sec-butyl, more preferably methyl or ethyl; c) n is the number of units of the calixarene ring and is comprised in the range between 4 and 16, preferably between 5 and 12; said calixarene being characterized in that in at least one of the n units of the calixarene ring, at least one of the substituents R1, R2, R3 and R4 contains at least one acid group of carboxylic type available for the reaction with a metal base, with the proviso that said acid group of carboxylic type is not contained in a unit of the calixarene ring derived from salicylic acid.

New Syntheses and Physical Properties of p-Alkylcalixarenes

Shinkai, Seiji,Nagasaki, Takeshi,Iwamoto, Koji,Ikeda, Atsushi,He, G.-X.,et al.

, p. 381 - 386 (2007/10/02)

Calixarenes (n=4, 6, and 8) bearing long p-alkyl groups (R=hexyl or dodecyl) have been synthesized by "direct" acylation of the p-position followed by silane reduction.The method is convenient and the yields are higher than those reported so far.Among them, p-hexanoylcalixarene showed a curious phase transition behavior; with raising the temperature it changed as crystal A -> liquid -> crystal B -> liquid.It was found on the basis of the solid 13C NMR spectra that this behavior is ascribed to a conformational change from "cone" (crystal A) to "partial cone" (crystal B).

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