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149699-75-2

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149699-75-2 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 149699-75-2 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,4,9,6,9 and 9 respectively; the second part has 2 digits, 7 and 5 respectively.
Calculate Digit Verification of CAS Registry Number 149699-75:
(8*1)+(7*4)+(6*9)+(5*6)+(4*9)+(3*9)+(2*7)+(1*5)=202
202 % 10 = 2
So 149699-75-2 is a valid CAS Registry Number.

149699-75-2Downstream Products

149699-75-2Relevant academic research and scientific papers

Nonorganometallic pathway of the Passerini reaction assisted by titanium tetrachloride

Carofiglio, Tommaso,Cozzi, Pier Giorgio,Floriani, Carlo,Chiesi-Villa, Angiola,Rizzoli, Corrado

, p. 2726 - 2736 (1993)

The Passerini reaction assisted by TiCl4 is a three component reaction (RNC, R′2CO, TiCl4) leading to C-C bond formation between the carbonyl and the isonitrile groups, and the formation of α-hydroxy amides. In order to clarify the mechanism of the reaction, we have isolated TiCl4RNC and TiCl4-R2CO adducts, {2,6-Me2C6H3NC)TiCl3] 2(μ-Cl)2}2> 2, [TiCl4{μ2-CO=C(OEt)CH2NC}]2, 3, [TiCl4{μ2-O=P(OEt)2CH2NC}] 2, 4, and [TiCl4{PhC(O)-C(O)Ph}], 5. Spectroscopic and X-ray analysis on 2 and 3 ruled out any insertion of the isocyanide into Ti-Cl bonds, as required by the accepted mechanism of this reaction. The reaction on the ketone- or isocyanide-TiCl4 adducts with the third component of the Passerini reaction led us to the isolation and full characterization of [mer-TiCl3(η3-OC(Mes)(H)C(Cl)=NCH 2C(OEt)=O], 6, [mer-TiCl3(η3-OC(Ph)(Me)C(Cl)=NCH 2C(OEt)=O], 7, [mer-TiCl3(n3-OC(Ph)(Me)C(Cl)=NCH2P(OEt) 2=O], 10, and [mer-TiCl3(η3-OC(Ph)(OCPh)C(Cl)=NCH 2C(OEt)=O], 12, derived from the reaction of MesCHO and PhCOMe with EtOOCCH2NC, of PhCOCH3 with O=P(OEt)2CH2NC, and PhCOCOPh with EtOOCH2NC, respectively. These are high yield reactions and form, as imposed by the planar assembled ligand, the mer-isomer only. The hydrolysis of 6, 7, 10, and 12 gave the expected α-hydroxy amide derivatives, 8, 9, 11, and 13, respectively. The overall mechanism of the TiCl4-assisted Passerini reaction can be described as the electrophilic activation of a carbonyl group by TiCl4 followed by the nucleophilic attack on the carbonylic carbon by the RNC nucleophile. Crystallographic details: 2 is monoclinic, space group P21/n, a = 13.943(1) A?, b = 8.045(1) A?, c = 12.141(1) A?, α = γ = 90°, β = 104.76(1)°, Z = 2, R = 0.048; 4 is monoclinic, space group P21/c, a = 12.961(1) A?, b = 11.770(1) A?, c = 10.917(1) A?, α = γ = 90°, β = 114.13(1)°, Z = 2, R = 0.049; 5 is triclinic, space group P1, a = 10.549(1) A?, b = 10.668(1) A?, c = 9.533(1) A?, α = 115.08(1)°, β = 115.47(1)°, γ = 95.01(1)°, Z = 2, R = 0.035; 7 is triclinic, space group P1, a = 9.731(2) A?, b = 10.552(3) A?, c = 8.978(2) A?, α = 96.66(2)°, β = 101.86(2)°, γ = 95.30(2)°, Z = 2, R = 0.042; 10 is monoclinic, space group P21/c, a = 11.503(2) A?, b = 14.095(2) A?, c = 15.110(2) A?, α = γ = 90°, β = 96.79(2)°, Z = 4, R = 0.116; 12 is triclinic, space group P1, a = 9.272(4) A?, b = 9.965(4) A?, c = 15.029(6) A?, α = 101.84(3)°, β = 104.12(3)°, γ = 99.53(3)°, Z = 2, R = 0.092.

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