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Tetracyclo[14.3.1.14,8.19,13]docosane-1(20),4(22),5,7,9,11,13(21),16,18-nonaene is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

24656-55-1

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24656-55-1 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 24656-55-1 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 2,4,6,5 and 6 respectively; the second part has 2 digits, 5 and 5 respectively.
Calculate Digit Verification of CAS Registry Number 24656-55:
(7*2)+(6*4)+(5*6)+(4*5)+(3*6)+(2*5)+(1*5)=121
121 % 10 = 1
So 24656-55-1 is a valid CAS Registry Number.

24656-55-1SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 11, 2017

Revision Date: Aug 11, 2017

1.Identification

1.1 GHS Product identifier

Product name Tetracyclo[14.3.1.12,6.19,13]docosa-1(20),2,4,6(22),9,11,13(21),16,18-nonaene

1.2 Other means of identification

Product number -
Other names [2.2.0]m,m,m-cyclophane

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

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

More Details:24656-55-1 SDS

24656-55-1Downstream Products

24656-55-1Relevant academic research and scientific papers

Small hydrocarbon cyclophanes: Synthesis, x-ray analysis and molecular modelling

Lahtinen, Tanja,Wegelius, Elina,Linnanto, Juha,Rissanen, Kari

, p. 2935 - 2941 (2007/10/03)

Small hydrocarbon cyclophanes, such as [2.2.0]m,m,m-cyclophane (20) and [2.2.0]p,m,m-cyclophane (21), are strained analogues of the well-known π-prismand [2.2.2]p,p,p-cyclophane (1). The synthetic route to these molecules is based on well-established cyclophane methodology which offers a general access to a whole family of hydrocarbon cyclophanes. Single crystal X-ray analysis and molecular modelling showed that the reduction of the ring size from 18-membered (1) to 14-membered (21) or 13-membered (20) has a substantial effect on the size and the shape of the cyclophane's cavity, thus blocking its ability to complex Ag+ ions. Wiley-VCH Verlag GmbH, 69451 Weinheim, Germany, 2002.

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