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Bicyclo[2.2.1]heptane, 7-chloro-, also known as 7-chlorobicyclo[2.2.1]heptane, is a halogenated organic compound with the molecular formula C7H11Cl. It is a derivative of bicyclo[2.2.1]heptane, a bicyclic hydrocarbon with a seven-membered ring structure. The presence of a chlorine atom at the 7-position introduces a halogenated functional group, which can significantly alter the compound's chemical properties and reactivity compared to its parent hydrocarbon. This chlorinated derivative may be used in various chemical syntheses, particularly in the pharmaceutical and agrochemical industries, as a building block for more complex molecules. Due to its potential applications and the presence of a halogen atom, it is important to consider its environmental impact and safety profile when handling and using Bicyclo[2.2.1]heptane, 7-chloro-.

765-80-0

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765-80-0 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 765-80-0 includes 6 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 3 digits, 7,6 and 5 respectively; the second part has 2 digits, 8 and 0 respectively.
Calculate Digit Verification of CAS Registry Number 765-80:
(5*7)+(4*6)+(3*5)+(2*8)+(1*0)=90
90 % 10 = 0
So 765-80-0 is a valid CAS Registry Number.

765-80-0SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 19, 2017

Revision Date: Aug 19, 2017

1.Identification

1.1 GHS Product identifier

Product name 7-chlorobicyclo[2.2.1]heptane

1.2 Other means of identification

Product number -
Other names -

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:765-80-0 SDS

765-80-0Downstream Products

765-80-0Relevant academic research and scientific papers

The reaction of some polycyclic halides with lihium p,p'-di-tert-butylbiphenyl

Stapersma, J.,Kuipers, P.,Klumpp, G. W.

, p. 213 - 218 (2007/10/02)

3-chloroquadricyclane (1), 2(4)-chlorosemibullvalene (2a), a series of 2-norbornyl halides and 4,4-dichlorotetracyclo2,8.03,6>octane (4) have been treated with lithium p,p'-di-tert-butylbiphenyl.Lihiation (2, norbornyl halides), lithiation with rearrangement (4) and lithiation with rearrangement followed by reduction to the cycloheptatrienyl trianion (1 -> 14) have been found to occur.

Temperature Effects on the Selectivity of ?-Radicals

Giese, Bernd,Stellmach, Joachim

, p. 3294 - 3302 (2007/10/02)

Bent ?-radicals 3a-i, generated from alkylmercuric salts 1 and/or peresters 2, were treated with a BrCCl3/CCl4 competition system at different temperatures.Exner-analysis of these selectivity data (table 1) shows, that radicals of sp2 type 3a-d and bridgehead radicals 3e-i follow different isoselective relationships (figure 1, 2).Reversal of the selectivity row occurs at 310 and 210 K, respectively.Above of these isoselective temperatures less shielded radicals are more selective than more shielded radicals because entropy effects overcompensate enthalpy effects (table 2).Comparison with ?-radicals 6 shows, that each type of carbon radicals follows an isoselective relationship by its own.

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