1123-60-0 Usage
Uses
Used in Chemical Industry:
Cyclopentane, 1,2,3,4,5-pentachlorois used as a chemical intermediate for the synthesis of other compounds in the chemical industry. Its unique structure with five chlorine atoms attached to the cyclopentane ring makes it a valuable building block for the production of various chemicals.
Used in Solvent Applications:
Due to its properties as a chlorinated hydrocarbon, Cyclopentane, 1,2,3,4,5-pentachlorocan be used as a solvent in specific applications within the chemical industry. Its ability to dissolve a wide range of substances makes it suitable for use in certain processes where a solvent with high solvency power is required.
Used in Pesticide Industry:
Cyclopentane, 1,2,3,4,5-pentachlorocan be used as a component in the formulation of pesticides, particularly those targeting soil-borne pests. Its chemical properties may provide effective control of pests while minimizing the impact on the environment and human health.
Used in Flame Retardant Industry:
The presence of multiple chlorine atoms in Cyclopentane, 1,2,3,4,5-pentachloromakes it a potential candidate for use in flame retardant applications. Its ability to slow down the combustion process can be utilized in the development of flame retardant materials for various industries, such as plastics, textiles, and construction.
Check Digit Verification of cas no
The CAS Registry Mumber 1123-60-0 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 1,1,2 and 3 respectively; the second part has 2 digits, 6 and 0 respectively.
Calculate Digit Verification of CAS Registry Number 1123-60:
(6*1)+(5*1)+(4*2)+(3*3)+(2*6)+(1*0)=40
40 % 10 = 0
So 1123-60-0 is a valid CAS Registry Number.
1123-60-0Relevant academic research and scientific papers
CYCLOPENTADIENYL-METAL BOND CLEAVAGE AND STEREOSPECIFIC BROMINATION. THE STRUCTURE OF (η-C5H5)2Ti(OOCPh)2 AND ITS REACTIONS WITH BROMINE
Lucas, C. Robert,Gabe, Eric J.,Lee, Florence L.
, p. 429 - 434 (2007/10/02)
The 13C and 1H nmr spectra as well as the X-ray structure determination for (η-C5H5)2Ti(OOCPh)2 are described.The compound crystallizes in space group P212121 with a = 7.5135, b = 12.5166, c = 21.1416 Angstroem, Z = 4, dcalcd = 1.40 g cm-3 (MoKα1, λ = 0.70932 Angstroem).The structure was solved with MULTAN using data collected at 115 K and refined to the final R = 0.059 for 1500 significant reflections.The molecule has two different carboxylate ligands, one of which has a Ti-O-C angle of 135.4(6) deg and longer Ti-O (1.976(5) Angstroem) and O-C (1.300(10) Angstroem) bonds while the other has a Ti-O-C angle of 157.0(7) deg with shorter Ti-O (1.913(6) Angstroem) and O-C (1.267(10) Angstroem) bonds.With bromine, ring cleavage occurs giving C5H5Br3 or C5H5Br5 in which bromination has occurred stereospecifically.The same reaction occurs with chlorine but not with iodine or iodine monochloride.Related reactions have been observed with (η-C5H5)2MCl2 (M = Ti, Zr, and V).A non-radical mechanism is proposed in which the LUMO and HOMO of Br2 interact simultaneously with one cyclopentadienyl ring and with the metal.This interaction is a consequence of the structure of (η-C5H5)2M(OOCPh)2.
