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<3S-(3α,4β,5α)>-4-amino-1--3-furanyl>-2(1H)-pyrimidinone is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

132523-69-4

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132523-69-4 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 132523-69-4 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,3,2,5,2 and 3 respectively; the second part has 2 digits, 6 and 9 respectively.
Calculate Digit Verification of CAS Registry Number 132523-69:
(8*1)+(7*3)+(6*2)+(5*5)+(4*2)+(3*3)+(2*6)+(1*9)=104
104 % 10 = 4
So 132523-69-4 is a valid CAS Registry Number.

132523-69-4Downstream Products

132523-69-4Relevant academic research and scientific papers

Nucleosides and nucleotides. 132. Synthesis and biological evaluations of ring-expanded oxetanocin analogues: Purine and pyrimidine analogues of 1,4-anhydro-2-deoxy-D-arabitol and 1,4-anhydro-2-deoxy-3-hydroxymethyl-D-arabitol

Kakefuda, Akio,Shuto, Satoshi,Nagahata, Takemitsu,Seki, Jun-Ichi,Sasaki, Takuma,Matsuda, Akira

, p. 10167 - 10182 (2007/10/02)

(2R)-2-C-(Adenin-9-yl)- 1,4-anhydro-2-deoxy-D-arabitol (2) and (2R, 3R)-2-C-(adenin-9-yl)- 1,4-anhydro- 2,3-dideoxy-3-C-hydroxymethyl-D-arabitol (3), and their 2,6-diaminopurine analogues 4 and 5 were synthesized from corresponding 1,4-anhydro-D-ribitol derivatives, which were readily obtained from D-glucose. The corresponding guanine isonucleosides 6 and 7 were obtained from 4 and 5 by enzymatic deamination with adenosine deaminase. Pyrimidine counterparts 8 and 9 were synthesized via construction of the pyrimidine moiety from amino derivatives of the 1,4-anhydro-D-arabitol derivatives. Antiviral activity of these ring-expanded derivatives of oxetanocins towards HSV-1, HSV-2, HCMV, and HBV in vitro was examined along with their cytotoxicity against L1210 and KB cells in vitro.

Synthesis and antiviral activity of novel isonucleoside analogs

Tino,Clark,Field,Jacobs,Lis,Michalik,McGeever-Rubin,Slusarchyk,Spergel,Sundeen,Tuomari,Weaver,Young,Zahler

, p. 1221 - 1229 (2007/10/02)

A series of branched-chain sugar isonucleosides was synthesized and evaluated for antiviral activity against herpesviruses. The preparation of homochiral [3S-(3α,4β,5α)]-2-amino-1,9-dihydro-9-[tetrahydro-4,5- bis(hydroxymethyl)-3-furanyl]-6H-purin-6-one (

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