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99314-01-9

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  • 99314-01-9 28H-4,18-(Methano[1,3]benzenomethano)-23,27-metheno-22H-dibenzo[n,w][1,4,7,10,13]pentaoxacyclotetracosin-29,32-diol,2,20,25,35-tetrakis(1,1-dimethylethyl)-6,7,9,10,12,13,15,16-octahydro-

    Cas No: 99314-01-9

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99314-01-9 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 99314-01-9 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 9,9,3,1 and 4 respectively; the second part has 2 digits, 0 and 1 respectively.
Calculate Digit Verification of CAS Registry Number 99314-01:
(7*9)+(6*9)+(5*3)+(4*1)+(3*4)+(2*0)+(1*1)=149
149 % 10 = 9
So 99314-01-9 is a valid CAS Registry Number.

99314-01-9SDS

SAFETY DATA SHEETS

According to Globally Harmonized System of Classification and Labelling of Chemicals (GHS) - Sixth revised edition

Version: 1.0

Creation Date: Aug 13, 2017

Revision Date: Aug 13, 2017

1.Identification

1.1 GHS Product identifier

Product name 4-TERT-BUTYL-CALIX[4]ARENE-CROWN-5-COMPLEX

1.2 Other means of identification

Product number -
Other names 4-TERT-BUTYLCALIX(4)-CROWN-5

1.3 Recommended use of the chemical and restrictions on use

Identified uses For industry use only.
Uses advised against no data available

1.4 Supplier's details

1.5 Emergency phone number

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Service hours Monday to Friday, 9am-5pm (Standard time zone: UTC/GMT +8 hours).

More Details:99314-01-9 SDS

99314-01-9Relevant articles and documents

Enhanced etherification of calix[4]arenes by microwave irradiation

Xu, Zhen,Lü, Zao Sheng,Chen, Lei

, p. 77 - 83 (2017/05/12)

Microwave irradiation has been found to be a highly efficient method for etherification of p-tert-butylcalix[4]arene with alkyl bromides or ditosylate. The corresponding products were obtained as a pure form in modest yield within short reaction time when

Synthesis of a cone-conformer bimodal calix[4]arene-crown-5 which forms a sensitive cesium ion sensing layer on gold-coated microcantilevers

Valluru, Gopikishore,Rahman, Shofiur,Georghiou, Paris E.,Dawe, Louise N.,Alodhayb, Abdullah N.,Beaulieu, Luc Y.

, p. 5868 - 5872 (2015/01/08)

A "bimodal" or upper- and lower-rim functionalized "calix-crown-5" reported herein was unexpectedly formed preferentially in a cone conformation. This was confirmed both by NMR spectroscopy and by single-crystal X-ray crystallography. The thioacetate functionalities on the new calix-crown-5 enabled it to form stable SAMs on the Au surface of a microcantilever, and a sensitive cesium ion sensor. This journal is

Facile synthesis of cone p-tert-butylcalix[4]arene-crown conformers

Alekseeva, Elena A.,Basok, Stepan S.,Mazepa, Alexander V.,Gren, Andrei I.

, p. 330 - 331 (2008/03/30)

The series of p-tert-butylcalix[4]arene-crowns in the cone conformation was synthesised in high yields under conditions producing disubstituted calix[4]arenes in the presence of K2CO3 in acetonitrile; the formation of calix-bis(crown)s and doubly(calix)-doubly(crown) in these reactions was established.

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