Cas 399564-65-9,{[(2-benzyloxycarbonylamino-6-oxo-1,6-dihydro-purin-9-yl)-acetyl]-[2-(9<i>H</i>-fluoren-9-ylmethoxycarbonylamino)-benzyl]-amino}-acetic acid <i>tert</i>-butyl ester

399564-65-9

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Basic information

Product Name: {[(2-benzyloxycarbonylamino-6-oxo-1,6-dihydro-purin-9-yl)-acetyl]-[2-(9H-fluoren-9-ylmethoxycarbonylamino)-benzyl]-amino}-acetic acid tert-butyl ester
Synonyms: {[(2-benzyloxycarbonylamino-6-oxo-1,6-dihydro-purin-9-yl)-acetyl]-[2-(9H-fluoren-9-ylmethoxycarbonylamino)-benzyl]-amino}-acetic acid tert-butyl ester
CAS NO:399564-65-9
Molecular Formula:
Molecular Weight: 783.841
EINECS: N/A
Product Categories: N/A

Chemical Properties

Melting Point: N/A
Boiling Point: N/A
Flash Point: N/A
Appearance: N/A
Density: N/A
Refractive Index: N/A
Storage Temp.: N/A
Solubility: N/A
CAS DataBase Reference: {[(2-benzyloxycarbonylamino-6-oxo-1,6-dihydro-purin-9-yl)-acetyl]-[2-(9H-fluoren-9-ylmethoxycarbonylamino)-benzyl]-amino}-acetic acid tert-butyl ester(CAS DataBase Reference)
NIST Chemistry Reference: {[(2-benzyloxycarbonylamino-6-oxo-1,6-dihydro-purin-9-yl)-acetyl]-[2-(9H-fluoren-9-ylmethoxycarbonylamino)-benzyl]-amino}-acetic acid tert-butyl ester(399564-65-9)
EPA Substance Registry System: {[(2-benzyloxycarbonylamino-6-oxo-1,6-dihydro-purin-9-yl)-acetyl]-[2-(9H-fluoren-9-ylmethoxycarbonylamino)-benzyl]-amino}-acetic acid tert-butyl ester(399564-65-9)

Safety Data

Hazard Codes: N/A
Statements: N/A
Safety Statements: N/A
WGK Germany:
RTECS:
HazardClass: N/A
PackingGroup: N/A
Hazardous Substances Data: 399564-65-9(Hazardous Substances Data)

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Check Digit Verification of cas no

The CAS Registry Mumber 399564-65-9 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 3,9,9,5,6 and 4 respectively; the second part has 2 digits, 6 and 5 respectively.
Calculate Digit Verification of CAS Registry Number 399564-65:
(8*3)+(7*9)+(6*9)+(5*5)+(4*6)+(3*4)+(2*6)+(1*5)=219
219 % 10 = 9
So 399564-65-9 is a valid CAS Registry Number.

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399564-65-9Relevant academic research and scientific papers

Hybridization properties of aromatic peptide nucleic acids: A novel class of oligonucleotide analogues

Fader, Lee D.,Tsantrizos, Youla S.

, p. 63 - 66 (2007/10/03)

(matrix presented) The synthesis of APNA-PNA chimeras containing all four DNA bases will be described. The hybridization properties of APNA-PNA chimeras with DNA and RNA are consistent with plausible intramolecular interactions that could preorganize the

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