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(E)-17-[N-(2-(tert-Butyloxycarbonylamino)ethyl)]-N-[N4-(benzyloxycarbonyl)cytosine-1-ylacetyl]glycinyloxy-4,7,10,13-tetraoxa-15-heptadecenoic acic is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

230617-99-9

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230617-99-9 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 230617-99-9 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 2,3,0,6,1 and 7 respectively; the second part has 2 digits, 9 and 9 respectively.
Calculate Digit Verification of CAS Registry Number 230617-99:
(8*2)+(7*3)+(6*0)+(5*6)+(4*1)+(3*7)+(2*9)+(1*9)=119
119 % 10 = 9
So 230617-99-9 is a valid CAS Registry Number.

230617-99-9Downstream Products

230617-99-9Relevant academic research and scientific papers

Convergent strategies for the attachment of fluorescing reporter groups to peptide nucleic acids in solution and on solid phase

Seitz, Oliver,Koehler, Olaf

, p. 3911 - 3925 (2007/10/03)

The site-selective conjugation of peptide nucleic acids (PNA) with fluorescent reporter groups is essential for the construction of hybridisation probes that can report the presence of a particular DNA sequence. This paper describes convergent methods for

Solid phase synthesis of protected peptide nucleic acids

Seitz, Oliver

, p. 4161 - 4164 (2007/10/03)

Boc/Z-protected PNA oligomers were synthesised on solid phase. The use of the allylic HYCRON resin allowed for the application of both Boc- and Fmoc-protecting groups. Highest yields were obtained when the monomeric building block was synthesised on solid phase rather than loaded as preformed unit. The selective attachment of fluorescent labels at the C-terminal (3') end demonstrated for the first time that further manipulations on protected PNA fragments are feasible.

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