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(1'R,2'R,3'S)-1-[2'-benzoyloxymethyl-3'-(hydroxymethyl)cyclobutyl]thymine is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

285138-30-9

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285138-30-9 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 285138-30-9 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 2,8,5,1,3 and 8 respectively; the second part has 2 digits, 3 and 0 respectively.
Calculate Digit Verification of CAS Registry Number 285138-30:
(8*2)+(7*8)+(6*5)+(5*1)+(4*3)+(3*8)+(2*3)+(1*0)=149
149 % 10 = 9
So 285138-30-9 is a valid CAS Registry Number.

285138-30-9Relevant academic research and scientific papers

Synthesis and hybridization property of oligonucleotides containing carbocyclic oxetanocins

Honzawa, Shinobu,Ohwada, Satoshi,Morishita, Yoshihiro,Sato, Kanae,Katagiri, Nobuya,Yamaguchi, Masahiko

, p. 2615 - 2627 (2007/10/03)

Oligonucleotides containing enantiomeric carbocyclic oxetanocins possessing adenine, thymine, guanine and cytosine were synthesized from an optically active cyclobutane derivative. Their hybridization properties with the complementary oligonucleotides were studied using melting point method, CD spectroscopy, and mixing curve method (Job plots). The artificial nucleotides possessing adenine, guanine and cytosine bases show tendency to form complexes more strongly with ribonucleotide than deoxyribonucleotide. These complexes are triplexes consisting of purine and pyrimidine in 1:2 ratio. Such triplex formation is observed both under high (1 M NaCl) and low salt conditions (0.1 M NaCl). (C) 2000 Elsevier Science Ltd.

Highly regio- and enantio-selective deacylation of carbocyclic 3',5'- di-O-acyloxetanocins by lipases

Katagiri, Nobuya,Morishita, Yoshihiro,Yamaguchi, Masahiko

, p. 2613 - 2616 (2007/10/03)

Carbocyclic (-)-3',5'-di-O-acyloxetanocin A and T were hydrolysed by lipase MY to give the corresponding carbocyclic (-)-3'-O-acyloxetanocins with high regioselectivity. Carbocyclic (±)-3',5'-di-O-acetyloxetanocin A was deacetylated by lipase MY to form t

High pressure in enzyme catalyzed organic reactions

Katagiri, Nobuya,Yamaguchi, Masahiko,Kaneko, Chikara

, p. 1023 - 1043 (2007/10/03)

Adenosine deaminase and lipases catalyzed hydrolysis under high pressure were described. The hydrolysis by both enzymes was facilitated by high pressures. This technique was used for the kinetical resolution of racemic highly modified nucleosides having biological activities.

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