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5,6,11,12-Tetrahydro-2,9-ethanodibenzo[a,e]cyclooctene is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

58002-98-5

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58002-98-5 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 58002-98-5 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 5,8,0,0 and 2 respectively; the second part has 2 digits, 9 and 8 respectively.
Calculate Digit Verification of CAS Registry Number 58002-98:
(7*5)+(6*8)+(5*0)+(4*0)+(3*2)+(2*9)+(1*8)=115
115 % 10 = 5
So 58002-98-5 is a valid CAS Registry Number.
InChI:InChI=1/C18H18/c1-2-14-4-6-16-8-7-15-5-3-13(1)11-17(15)9-10-18(16)12-14/h3-6,11-12H,1-2,7-10H2

58002-98-5SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 18, 2017

Revision Date: Aug 18, 2017

1.Identification

1.1 GHS Product identifier

Product name (2.2.2)(1,2,4)Cyclophane

1.2 Other means of identification

Product number -
Other names 1,2,4-<Paracyclophan

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:58002-98-5 SDS

58002-98-5Relevant academic research and scientific papers

Macro Rings. 49. Use of Transannular Reactions to Add Bridges to Paracyclophane

Truesdale, E.A.,Cram, Donald J.

, p. 3974 - 3981 (2007/10/02)

New transannular reactions were used to introduce additional bridges into paracyclophane (1).With CH2O-HCl, 4-acetylparacyclophane (3) gave (55percent) 4-acetyl-13-(chloromethyl)paracyclophane (4), whose substituents are pseudogem to one an

Cyclophanes, XIII. On the Chemical Behaviour of (1,2,4)Cyclophane

Murad, Abo El-Fetouh El-Sayed,Hopf, Henning

, p. 2358 - 2371 (2007/10/02)

(1,2,4)Cyclophane (10) has been prepared by several routes from dimethylparacyclophane-4,13-dicarboxylate (5) and subjected to the following reactions: pyrolysis in p-diisopropylbenzene and dimethyl maleate (formation of 13 and 16, respectivel

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