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{2-[bis-(4-methoxy-phenyl)-phenyl-methoxy]-ethylamino}-acetic acid methyl ester is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

884347-75-5

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884347-75-5 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 884347-75-5 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 8,8,4,3,4 and 7 respectively; the second part has 2 digits, 7 and 5 respectively.
Calculate Digit Verification of CAS Registry Number 884347-75:
(8*8)+(7*8)+(6*4)+(5*3)+(4*4)+(3*7)+(2*7)+(1*5)=215
215 % 10 = 5
So 884347-75-5 is a valid CAS Registry Number.

884347-75-5Relevant academic research and scientific papers

Dda helicase unwinds a DNA-PNA chimeric substrate: Evidence for an inchworm mechanism

Spurling, Travis L.,Eoff, Robert L.,Raney, Kevin D.

, p. 1816 - 1820 (2008/03/13)

Helicases are ubiquitous enzymes involved in all aspects of DNA metabolism including replication, repair, recombination, and transcription. The mechanism of the bacteriophage T4 Dda helicase was investigated by preparing a DNA-PNA chimeric substrate. Surp

Peptide nucleic acids and their phosphonate analogues: Synthesis and hybridization properties

Efimov,Buryakova,Choob,Chakhmakhcheva

, p. 618 - 630 (2007/10/03)

The synthesis of a series of DNA mimics-peptide nucleic acids, phosphonate analogues of peptide nucleic acids, and their hybrids - is described. The preparative synthesis of the corresponding monomers and the solid phase automated synthesis of oligomers-mimics are developed. Modified phosphonate analogues of peptide nucleic acids, in particular, chiral derivatives and those with additional hydroxyl groups in the side chains of the backbone, as well as pyrene derivatives of peptide nucleic acids and their phosphonate analogues, are prepared. The affinity of the resulting oligomers specifically to hybridize to DNA and RNA complementary chains is studied. It is shown that phosphonate analogues of peptide nucleic acids and their hybrids with peptide nucleic acids can form complexes with the DNA and RNA complementary strands, the stability of the complexes increasing in parallel with the increase in the number of peptide nucleic acid residues in the chain of the mimic. This property, along with good water solubility, provides the precondition for further evaluation of these compounds as antisense and antigene agents.

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