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51339-33-4

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51339-33-4 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 51339-33-4 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 5,1,3,3 and 9 respectively; the second part has 2 digits, 3 and 3 respectively.
Calculate Digit Verification of CAS Registry Number 51339-33:
(7*5)+(6*1)+(5*3)+(4*3)+(3*9)+(2*3)+(1*3)=104
104 % 10 = 4
So 51339-33-4 is a valid CAS Registry Number.

51339-33-4Relevant academic research and scientific papers

Glutamic acid as a new linker for attachment of alcohols to solid support

Subra, Gilles,Amblard, Muriel,Martinez, Jean

, p. 9221 - 9223 (2002)

We took advantage of pyroglutamic cyclization of glutamic acid to investigate the use of this amino acid as a linker for the attachment of alcohols. As a first example, we reported the solid-phase synthesis of dimers on a 3,3′-diaminodiphenylmethanol.

Iodine-catalyzed disproportionation of aryl-substituted ethers under solvent-free reaction conditions

Jereb, Marjan,Vrazic, Dejan

, p. 1978 - 1999 (2013/05/22)

Iodine was demonstrated to be an efficient catalyst for disproportionation of aryl-substituted ethers under solvent-free reaction conditions. Variously substituted 1,1,1′,1′-tetraaryldimethyl ethers were transformed into the corresponding diarylketone and diarylmethane derivatives. I 2-catalyzed transformation of 4-methoxyphenyl substituted ethers yielded mono- and dialkylated Friedel-Crafts products as well. Treatment of trityl alkyl and trityl benzyl ethers with a catalytic amount of iodine produced triphenylmethane and the corresponding aldehydes and ketones. The electron-donating substituents facilitated the reaction, while the electron-withdrawing groups retarded it; the difference in reactivity is not very high. Such an observation may be in favour of hydride transfer, predominantly from the less electron rich side of the ether with more stable carbocation formation. With the isotopic studies it was established that a substantial portion of the C-H bond scission took place in the rate-determining step, while the carbonyl oxygen atom originated from the starting ether, and not from the air. The transformation took place under air and under argon, and HI was not a functioning catalyst.

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