Welcome to LookChem.com Sign In|Join Free
  • or
5-allyl-25-hydroxy-26,27,28-tribenzoyloxycalix<4>arene 1,3-alternate conformer is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

106750-84-9

Post Buying Request

106750-84-9 Suppliers

Recommended suppliers

  • Product
  • FOB Price
  • Min.Order
  • Supply Ability
  • Supplier
  • Contact Supplier

106750-84-9 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 106750-84-9 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,0,6,7,5 and 0 respectively; the second part has 2 digits, 8 and 4 respectively.
Calculate Digit Verification of CAS Registry Number 106750-84:
(8*1)+(7*0)+(6*6)+(5*7)+(4*5)+(3*0)+(2*8)+(1*4)=119
119 % 10 = 9
So 106750-84-9 is a valid CAS Registry Number.

106750-84-9Relevant academic research and scientific papers

Synthesis of calixarene-capped carbosilane dendrimers

Lambert, Joseph B.,Kang, Seung-Hyun,Kuangbiao, Ma.,Liu, Chunqing,Condie, Allison G.

supporting information; experimental part, p. 2527 - 2532 (2009/09/25)

A new class of polycalix[4]arene hosts has been constructed based on a carbosilane dendrimer architecture, in which each dendritic branch terminates with a calix[4]arene entity. This study reports the synthesis and characterization of the zeroth generatio

CALIXARENES 12 THE SYNTESIS OF FUNCTIONALIZED CALIXARENES

Gutsche, C. David,Lin, Lee-Gin

, p. 1633 - 1640 (2007/10/02)

Procedures are described for the removal of the p-t-butyl groups from p-t-butylcalixarene, p-t-butylcalixarene, and p-t-butylcalixarene and the introduction of functional groups in their place.Although attempts to functionalize the p-positions of the calixarenes have generally failed, the corresponding methyl ethers are amenable to facile acetylation to provide syntheses of the p-acetyl-, p-carboxy-, and p-carbomethoxycalixarenes and calixarenes.Acetylation and benzoylation of calixarene and calixarene occur at the phenolic oxygens rather than the p-positions, leading under most reaction conditions to the completely O-substituted product.Calixarene reacts with benzoyl chloride in the presence of pyridine, however, to yield the tribenzoate.Conversion of the tribenzoate to the corresponding tribenzoyloxy monoallyl ether followed by a Claisen rearrangement and hydrolysis yields monoallylcalixarene, a compound of particular interest because of its potential for the synthesis of calixarenes containing a single substituent on the "upper rim".

Post a RFQ

Enter 15 to 2000 letters.Word count: 0 letters

Attach files(File Format: Jpeg, Jpg, Gif, Png, PDF, PPT, Zip, Rar,Word or Excel Maximum File Size: 3MB)

1 Customer Service

What can I do for you?
Get Best Price

Get Best Price for 106750-84-9