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Cyclopropylium is a highly reactive, three-membered cyclic carbocation with the molecular formula C3H5+. It is an unstable, highly strained species due to the presence of a three-membered ring, which results in significant angle strain. Cyclopropylium is a powerful electrophile and can readily undergo nucleophilic attack, making it a valuable intermediate in organic synthesis. It is generated in situ and is not typically isolated due to its high reactivity. The cyclopropylium ion plays a significant role in various chemical reactions, such as cyclopropanation, where it reacts with alkenes to form cyclopropane derivatives. Despite its instability, cyclopropylium has been the subject of extensive research, and its properties and reactivity have been well-documented in the field of organic chemistry.

1724-43-2

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1724-43-2 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 1724-43-2 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 1,7,2 and 4 respectively; the second part has 2 digits, 4 and 3 respectively.
Calculate Digit Verification of CAS Registry Number 1724-43:
(6*1)+(5*7)+(4*2)+(3*4)+(2*4)+(1*3)=72
72 % 10 = 2
So 1724-43-2 is a valid CAS Registry Number.

1724-43-2SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 17, 2017

Revision Date: Aug 17, 2017

1.Identification

1.1 GHS Product identifier

Product name cyclopropylium

1.2 Other means of identification

Product number -
Other names Cyclopropylkation

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:1724-43-2 SDS

1724-43-2Downstream Products

1724-43-2Relevant academic research and scientific papers

Ion-Molecule Reaction of CO2+ with Butane and Isobutane at Thermal Energy

Tsuji, Masaharu,Matsumura, Ken-ichi,Funatsu, Tsuyoshi,Nishimura, Yukio,Obase, Hiroshi,et al.

, p. 2864 - 2870 (2007/10/02)

Rate constants and product ion distributions have been determined for thermal energy reactions of CO+2 with n-C4H10 and i-C4H10 by using an ion-beam apparatus.The total rate constants are (9.8+/-2.0)*10-10 and (1.0+/-0.2)*10-9 cm3 s-1 for n-C4H10 and i-C4H10, respectively.These values amount to about 75percent of the collision rate constants estimated from the Langevin theory.C4H+9, C3H+n (n=5-7), and C2H+n (n=3-5) are produced from n-C4H10 with branching ratios of 6, 56, and 38percent, while C4H+9 and C3H+n (n=5-7) are formed from i-C4H10 with branching ratios of 7 and 93percent, respectively.The lack of C2H+n fragments from i-C4H10 is attributed to a low probability of significant rearrangement of chemical bonds for the formation of the C2H+n fragments.The product ion distribution in the CO+2/n-C4H10 reaction is in good agreement with that predicted from the fragmentation pattern of n-C4H+10 at 13.78 eV, indicating that the CO+2/n-C4H10 reaction proceeds through a near-resonant charge transfer without momentum transfer.

Laser photodissociation of C7H7+ created through multiphoton ionization of para-chlorotoluene

Lablanquie, Pascal,Ohashi, Kazuhiko,Nishi, Nobuyuki

, p. 399 - 408 (2007/10/02)

The nature of the C7H7+ ion created through resonant dissociative multiphotoionization of para-chlorotoluene by an ultraviolet (UV) laser was investigated thanks to its interaction with a second laser beam.The dissociation pattern corresponding to one or several photon absorption could be observed.Cross section for the one-photon absorption in the 265/530 nm range revealed the presence of the tropylium and benzyl isomers and suggested they possessed substantial internal energy.This was confirmed by the study of the C7H7+ + hν C5H5+ + C2H2 reaction, and more precisely of its rate and of the kinetic energy released.A ladder switch mechanism for the three-photon dissociative ionization of para-chlorotoluene leading to C7H7+ is shown to agree with our results.

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