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[8-(2-benzyloxycarbonylamino-ethoxy)-2-oxo-2,9-dihydro-10-oxa-1,3,9-triaza-anthracen-3-yl]-acetic acid is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

476454-43-0

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476454-43-0 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 476454-43-0 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 4,7,6,4,5 and 4 respectively; the second part has 2 digits, 4 and 3 respectively.
Calculate Digit Verification of CAS Registry Number 476454-43:
(8*4)+(7*7)+(6*6)+(5*4)+(4*5)+(3*4)+(2*4)+(1*3)=180
180 % 10 = 0
So 476454-43-0 is a valid CAS Registry Number.

476454-43-0Relevant articles and documents

Synthesis of amino- and guanidino-G-clamp PNA monomers

Ausin, Cristina,Ortega, Jose-Antonio,Robles, Jordi,Grandas, Anna,Pedroso, Enrique

, p. 4073 - 4075 (2007/10/03)

(matrix presented) Syntheses of the protected amino- and guanidino-G-clamp PNA monomers, 9a and 9b, respectively, have been accomplished in eight steps from 5-bromouracil. Enhanced stacking interactions and additional hydrogen bonds with guanine should in

High-Affinity Peptide Nucleic Acid Oligomers Containing Tricyclic Cytosine Analogues

Rajeev, Kallanthottathil G.,Maier, Martin A.,Lesnik, Elena A.,Manoharan, Muthiah

, p. 4395 - 4398 (2007/10/03)

(Matrix Presented) Peptide nucleic acid (PNA) monomers containing the tricyclic cytosine analogues phenoxazine, 9-(2-aminoethoxy)phenoxazine (G-clamp), and 9-(3-aminopropoxy)phenoxazine (propyl-G-clamp) have been synthesized. The modified nucleobases were

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