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Triphenylstannane-d1, also known as (triphenyl-2H-tin), is a deuterated organotin compound with the chemical formula (C6H5)3SnD. It is a derivative of triphenylstannane, where one hydrogen atom is replaced by a deuterium atom. triphenylstannane-d1 is primarily used as a reagent in organic synthesis, particularly in the formation of carbon-carbon bonds and as a reducing agent. Triphenylstannane-d1 is also employed in the synthesis of various organotin compounds and as a tracer in chemical reactions to study reaction mechanisms and kinetics. Due to its deuterium content, it can provide valuable information on the isotopic distribution in chemical products, which is useful in both academic research and industrial applications.

6181-00-6

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6181-00-6 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 6181-00-6 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 6,1,8 and 1 respectively; the second part has 2 digits, 0 and 0 respectively.
Calculate Digit Verification of CAS Registry Number 6181-00:
(6*6)+(5*1)+(4*8)+(3*1)+(2*0)+(1*0)=76
76 % 10 = 6
So 6181-00-6 is a valid CAS Registry Number.

6181-00-6Relevant academic research and scientific papers

INTERET DE LA DEUTERIATION DES MOLECULES ORGANOSTANNIQUES EN RMN DE 119Sn. II. RELATION DE TYPE KARPLUS POUR 3J(SnD) ET STEREOCHIMIE DE DEUTERIOSTANNATION DE QUELQUES HYDROCARBURES ETHYLENIQUES

Quintard, Jean-Paul,Degueil-Castaing, Marie,Barbe, Bernard,Petraud, Michel

, p. 41 - 62 (1982)

Whenever selective deuterium labelling is easily performed a new proficiency is given to FT 119Sn NMR by the determination of the angular dependence of 3J(SnD).Using model molecules with structures being checked by other methods, the angular dependence of 3J(SnD) has been shown to follow a Karplus-like relationship.Illustrative examples for the qualitative and quantitative analysis of diastereoisomeric organotin compounds are described.This method allows for instance, a fast and convenient determination of the stereochemistry of alkene deutero- and hydro-stannations.

A General Rhodium Catalyst for the Deuteration of Boranes and Hydrides of the Group 14 Elements

Esteruelas, Miguel A.,Martínez, Antonio,Oliván, Montserrat,Vélez, Andrea

, p. 15693 - 15698 (2020/12/02)

Pinacolborane, catecholborane, triethylsilane, triphenylsilane, dimethylphenylsilane, 1,1,1,3,5,5,5-heptamethyltrisiloxane, triethylgermane, triphenylgermane, and triphenylstannane deuterated at the heteroatom position have been catalytically prepared in

The reactions of Ir(CO)Cl(PPh3)2 with HSnPh 3

Adams, Richard D.,Fang, Fang,Smith, Mark D.,Zhang, Qiang

, p. 2904 - 2909 (2011/08/09)

A reinvestigation of the reaction of Ir(CO)Cl(PPh3)2, 1 with HSnPh3 has revealed that the oxidative-addition product Ir(CO)Cl(PPh3)2(H)(SnPh3), 2 has the H and SnPh3 ligands in cis-related coordination sites. Compound 2 reacts with a second equivalent of HSnPh3 by a Cl for H ligand exchange to yield the new compound H2Ir(CO)(SnPh3)(PPh 3)2, 3. Compound 3 contains two cis- related hydride ligands. Under an atmosphere of CO, 1 reacts with HSnPh3 to replace the Cl ligand with SnPh3 and one of the PPh3 ligands with a CO ligand and also adds a second equivalent of CO to yield the 5-coordinate complex Ir(CO)3(SnPh3)(PPh3), 4. Compound 4 reacts with HSnPh3 by loss of CO and oxidative addition of the Sn-H bond to yield the 6-coordinate complex HIr(CO)2(SnPh 3)2(PPh3), 5 that contains two trans-positioned SnPh3 ligands.

Efficient syntheses of four stable-isotope labeled (1R)-menthyl (1S,2S)-(+)-2-phenylcyclopropanecarboxylates

Keliher, Edmund J.,Burrell, Richard C.,Chobanian, Harry R.,Conkrite, Karina L.,Shukla, Rajesh,Baldwin, John E.

, p. 2777 - 2784 (2008/09/16)

Many carbenoid cyclopropanation reactions promoted by chiral catalysts give product mixtures reflecting impressive diastereo- and enantioselectivities. Few provide a single chiral product efficiently. This limitation has been overcome in cyclopropanations of styrene and isotopically labeled styrenes with α-diazoacetates. Convenient syntheses on a 20 g scale of each of four chiral isotopically labeled (1R)-menthyl (1S,2S)-2- phenylcyclopropanecarboxylates (the 1-d-3-13C, 1,(3S)-d2, 1,2,(3S)-d3, and 1,3,3-d3 isotopomers) of better than 99% ee have been realized. The Royal Society of Chemistry 2006.

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