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Mo(CO)3(CN(i-Pr)2)Br(P(C6H5)3) is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

350686-68-9

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350686-68-9 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 350686-68-9 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 3,5,0,6,8 and 6 respectively; the second part has 2 digits, 6 and 8 respectively.
Calculate Digit Verification of CAS Registry Number 350686-68:
(8*3)+(7*5)+(6*0)+(5*6)+(4*8)+(3*6)+(2*6)+(1*8)=159
159 % 10 = 9
So 350686-68-9 is a valid CAS Registry Number.

350686-68-9Downstream Products

350686-68-9Relevant academic research and scientific papers

Metallathiirenes. 3.1 thiocarbamoyl and alkoxythiocarbonyl complexes of molybdenum(II) and tungsten(II)

Anderson, Stephen,Cook, Darren J.,Hill, Anthony F.

, p. 2468 - 2476 (2001)

Synthetic routes to thiocarbamoyl (thiocarboxamide) complexes of divalent molybdenum and tungsten are reported: The reaction of fac-[Mo(CO)3(NCMe)3] with N,N-dimethyl thiocarbamoyl chloride (Me2NC(=S)Cl) at low temperature provides a thermally labile intermediate (1) presumed on the basis of subsequent transformations to be [Mo(η2-SCNMe2)-Cl(CO)3(NCMe)]. Reactions of 1 with K[HB(pz)3] (pz = pyrazol-1-yl), NaC5H5, bipy, or tmeda provide the complexes [Mo(η2-SCNMe2)(CO)2{HB(pz)3}] (2), [Mo(η2-SCNMe2)(CO)2(η-C5 H5)] (3), [Mo(η2-SCNMe2)Cl(CO)2(bipy)] (4), and [Mo(η2-SCNMe2)Cl(CO)2(tmeda)] (5), respectively. The complex cis,cis,trans-[Mo(η2-SCNMe2)Cl(CO)2 (PPh3)2] (6) results from the oxidative addition of Me2NC(=S)Cl to [Mo(NCMe)2(CO)2(PPh3)2] and is one of two isomers obtained from the reaction of 1 with PPh3. The complex 2 may also be obtained from reaction of (i) K[Mo(CO)3{HB(pz)3}] with Me2NC(=S)Cl; (ii) [Mo(CO)3(η6-C7H8)] with Me2NC(=S)Cl and K[HB(pz)3]; and (iii) K[HB(pz)3] with either 5 or 6. Sequential treatment of either [Mo(CO)3-(NCMe)3] or [Mo(CO)3(η6-C7H8)] with ClC(=S)OR (R = C6H4Me-4, C6H5) and K[HB(pz)3] provides the complexes [Mo(η2-SCOR)(CO)2{HB(pz)3}] [R = C6H4Me-4 (7a), C6H5 (7b)]. Attempts to prepare a mononuclear thiocarbamoyl complex by addition of elemental sulfur or propene episulfide to the aminomethylidyne complex [Mo(≡CNiPr2)(CO)2{HB(pz)3}] (8) were unsuccessful; however addition of [Fe2(CO)9] to 8 provided the thermally unstable complex [MoFe(μ-CNiPr2)(CO)5{HB(pz)3}] (9), which reacts with sulfur to provide the heterobimetallic bridging thiocarbamoyl complex [MoFe(μ-SCNiPr2)(CO)5{HB(pz)3}] (10). Treating fac-[W(CO)3(NCMe)3] sequentially with Me2NC(=S)Cl and K[HB(pz)3] provided [W(η2-SCNMe2)(CO)2{HB(pz)3}] (11); however replacing Me2NC(=S)Cl with ClC(=S)OC6H4-Me-4 led to [WCl(CO)3{HB(pz)3}] (12).

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