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35390-18-2

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35390-18-2 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 35390-18-2 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 3,5,3,9 and 0 respectively; the second part has 2 digits, 1 and 8 respectively.
Calculate Digit Verification of CAS Registry Number 35390-18:
(7*3)+(6*5)+(5*3)+(4*9)+(3*0)+(2*1)+(1*8)=112
112 % 10 = 2
So 35390-18-2 is a valid CAS Registry Number.

35390-18-2Relevant academic research and scientific papers

Ruthenium Hydride Catalyzed Silylvinylation of Internal Alkynes Using Ethylene as an Additive

Wilson, Robert J.,Kaminsky, Lauren,Ahmed, Ijaz,Clark, Daniel A.

, p. 8290 - 8299 (2015/09/01)

An efficient synthetic strategy for the regiospecific silylvinylation of internal alkynes is described. This transformation is catalyzed by RuHCl(CO)(SIMes)PPh3 and provides a net 5-exo-dig trans-silylvinylation of internal alkynes. Ethylene wa

Regioselective addition reactions of propargyl bromides to carbonyl compounds with gallium catalyzed by indium

Lee, Phil Ho,Kim, Hyun,Lee, Kooyeon

, p. 1219 - 1222 (2007/10/03)

Reactions of organogallium reagents generated from propargyl bromides having substituents at the γ-position and gallium in the presence of 5 mol % of indium with aldehydes and ketones selectively produced homoallenyl alcohols in good to excellent yields.

A highly atom efficient, solvent promoted addition of tetraallylic, tetraallenic, and tetrapropargylic stannanes to carbonyl compounds

McCluskey,Muderawan,Muntari,Young

, p. 7811 - 7817 (2007/10/03)

Tetraallylic, tetraallenic, and tetrapropargylic stannanes (0.25 equiv) react with aldehydes in methanol to provide unsaturated alcohols in good to excellent yields (56-99%). These reactions proceed exclusively with allylic rearrangement for tetra(2-butenyl)tin 2b and tetra(1,2-butadienyl)-tin 16c and predominantly with allylic rearrangement for tetrapropadienyltin 16a and tetra(2-butynyl)tin 6e. Allylation reactions also proceeded smoothly with reactive ketones such as ethyl pyruvate (9a) and cyclohexanone (9b). The corresponding TFA-catalyzed reactions of dimethyl acetals 4d and 4e are regiospecific with allylic rearrangement.

On pentaorganylstiborane. III. Regio- and diastereoselective additions of acetylenic and allenic organoantimony compounds to aldehydes

Zhang, Li-Jun,Mo, Xue-Sheng,Huang, Yao-Zeng

, p. 77 - 86 (2007/10/02)

The reaction of propargyl bromide (4a) with tributylstibine gave allenyltributylstibonium bromide (5), and its corresponding pentaorganylstiborane reacted with aldehyde to give homopropargylic alcohol (10a) exclusively in good yield.However, the reaction

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