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103594-89-4

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103594-89-4 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 103594-89-4 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,0,3,5,9 and 4 respectively; the second part has 2 digits, 8 and 9 respectively.
Calculate Digit Verification of CAS Registry Number 103594-89:
(8*1)+(7*0)+(6*3)+(5*5)+(4*9)+(3*4)+(2*8)+(1*9)=124
124 % 10 = 4
So 103594-89-4 is a valid CAS Registry Number.

103594-89-4Relevant academic research and scientific papers

A general palladium-catalyzed cross-coupling of aryl fluorides and organotitanium (IV) reagents

He, Xiao-Yun

, p. 823 - 832 (2021/07/19)

Pd(OAc)2/1-[2-(di-tert-butylphosphanyl)phenyl]-4-methoxy-piperidine was demonstrated to effectively catalyze cross-coupling of aryl fluoride and aryl(alkyl) titanium reagent. Both electron-deficient and electron-rich aryl fluoride can react effectively with nucleophile and provide extensive functional groups tolerance. 2-Arylated product was realized by selective activation of the C–F bond. Graphic abstract: [Figure not available: see fulltext.].

Synthesis of Chiral α-CF3-Substituted Benzhydryls via Cross-Coupling Reaction of Aryltitanates

Varenikov, Andrii,Shapiro, Evgeny,Gandelman, Mark

supporting information, p. 9386 - 9391 (2020/12/21)

We describe a highly efficient approach toward α-CF3-substituted benzhydryls thanks to the employment of organotitanium(IV) based nucleophiles. The use of commercially available anesthetic halothane as a cheap fluorinated building block in a sequential one-pot nickel-catalyzed enantioselective cross-coupling reaction of aryl titanates allowed for the synthesis of chiral α-CF3-substituted benzhydryls in good yields and excellent enantioselectivities. Alternatively, α-CF3-benzyl bromides could be employed under similar conditions to obtain the same family of compounds in higher yields and excellent selectivities. A benzhydryl moiety is a common motif in many biologically active compounds, and their enantioenriched fluorinated analogs should be of great interest in the search for novel drugs and agrochemicals.

Catalytic Enantioselective Arylation and Heteroarylation of Ketones with Organotitanium Reagents Generated In Situ

Matsuda, Atsushi,Ushimaru, Tomoya,Kobayashi, Yusuke,Harada, Toshiro

supporting information, p. 8605 - 8609 (2017/06/30)

A practical and useful, catalytic enantioselective method has been developed for the synthesis of tertiary diaryl and aryl heteroaryl carbinols starting from commercially available aromatic ketones and aryl or heteroaryl bromides. In this method, organotitanium reagents are generated in situ from the bromides by lithiation with nBuLi followed by transmetallation of the resulting organolithiums with ClTi(OiPr)3. Treatment of the ketones with the titanium reagents in the presence of (R)-3-(3,5-bistrifluoromehthylphenyl)-1,1′-bi-2-naphthol (BTFP-BINOL) affords the corresponding tertiary alcohols in high enantioselectivities and yields. The reaction can also start with furan and 2-thienyllithium. The method is operationally simple and can be conducted on a 10-mmol scale without any difficulties.

Nickel-catalyzed substitution reactions of propargyl halides with organotitanium reagents

Li, Qing-Han,Liao, Jung-Wei,Huang, Yi-Ling,Chiang, Ruei-Tang,Gau, Han-Mou

, p. 7634 - 7642 (2014/12/11)

A simple and mild catalytic coupling reaction of propargyl halides with organotitanium reagents is reported. The reaction of propargyl bromide with organo-titanium reagents mediated by NiCl2(2 mol%) and PCy3(4 mol%) in CH2

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