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18192-28-4

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18192-28-4 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 18192-28-4 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 1,8,1,9 and 2 respectively; the second part has 2 digits, 2 and 8 respectively.
Calculate Digit Verification of CAS Registry Number 18192-28:
(7*1)+(6*8)+(5*1)+(4*9)+(3*2)+(2*2)+(1*8)=114
114 % 10 = 4
So 18192-28-4 is a valid CAS Registry Number.

18192-28-4Relevant articles and documents

Tetrahedral Silicon-Centered Dibenzoylmethanatoboron Difluorides: Synthesis, Crystal Structure, and Photophysical Behavior in Solution and the Solid State

Kononevich, Yuriy N.,Temnikov, Maxim N.,Korlyukov, Alexander A.,Volodin, Alexander D.,Dorovatovskii, Pavel V.,Sazhnikov, Viacheslav A.,Safonov, Andrey A.,Ionov, Dmitriy S.,Ivanov, Anatoly A.,Surin, Nikolay M.,Svidchenko, Evgeniya A.,Muzafarov, Aziz M.

, p. 1111 - 1119 (2020/04/07)

Four tetrahedral silicon-centered derivatives of dibenzoylmethanatoboron difluoride (DBMBF2) were synthesized and characterized. Their structural and optical features both in solution and the solid state were investigated by using X-ray crystal

Enantioselective syntheses of 2-arylpropanoic acid non-steroidal antiinflammatory drugs and related compounds

Hamon, David P.G.,Massy-Westropp, Ralph A.,Newton, Josephine L.

, p. 12645 - 12660 (2007/10/02)

(S)-2-[4′-(2″-Methylpropyl)phenylpropanoic acid (ibuprofen) and (S)-2-(3′-benzoylphenyl)propanoic acid (ketoprofen) have been synthesised in high enantiomeric excess. Control of stereochemistry was achieved by a combination of Sharpless epoxidalion followed by catalytic hydrogenolysis of the introduced benzylic epoxide oxygen bond. Also, the coupling of organic compounds in the presence of palladium with enantiopure 2-(3-iodophenyl)propanoic and 2-(4-iodophenyl)propanoic acids, prepared by the methodology above, is a general method for the synthesis of optically active arylpropanoic acids.

Etude spectroscopique des p-trimethylsilyl, p-trimethylgermyl et p-trimethylstannylacetophenones

Maire, Jean-Claude,Marrot, Jean,Nabet, Roger

, p. 429 - 434 (2007/10/02)

Acylation of phenyltrimethylstannane in Friedel and Crafts reaction leads exclusively to cleavage of the tin-carbon bond.However, p-trimethylsilylacetophenone and its germanium and tin analogs have been sinthesized by reaction of the Grignard derivative o

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