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5'-O-DMT-N4-Ac-dC

Names

[ CAS No. ]:
100898-63-3

[ Name ]:
5'-O-DMT-N4-Ac-dC

[Synonym ]:
DMT-NAC-DC
N4-Acetyl-2'-Deoxy-5'-O-Dmt-D-Cytidine
N-ACETYL-5'-O-[BIS(4-METHOXYPHENYL)-PHENYLMETHYL]-2'-DEOXY-CYTIDINE
DMT-Ac-dC
N-ACETYL-5'-O-[BIS(4-METHOXYPHENYL)PHENYLMETHYL]-2'-DEOXY-CYTIDINE
N4-ACETYL-2'-DEOXY-5'-O-DMT-CYTIDINE
N-Acetyl-5'-O-(4,4'-dimethoxytrityl)-2'-deoxycytidine
5'-O-(4,4'-Dimethoxytrityl)-N4-acetyl-2'-deoxycytidine
5'-O-dimethoxytrityl-4-N-acetyl-2'-deoxycytidine
DMT-N4-Ac-dC
N4-Acetyl-2'-deoxy-5'-O-DMT-D-cytidine
5'-DMTr-N4-acetyl-2'-deoxycytidine
N4-Acetyl-2'-deoxy-5'-O-DMT-cytidine
N4-ACETYL-2'-DEOXY-5'-O-[BIS(4-METHOXYPHENYL)PHENYLMETHYL]-CYTIDINE
5'-DMT-N4-Ac-dC

Biological Activity

[Description]:

5'-O-DMT-N4-Ac-dC (N4-Acetyl-2'-deoxy-5'-O-DMT-cytidine, compound 7), a deoxynucleoside, can be used to synthesize of dodecyl phosphoramidite which is the raw material for dod‐DNA (amphiphilic DNA containing an internal hydrophobic region consisting of dodecyl phosphotriester linkages) synthesis[1][2].

[Related Catalog]:

Signaling Pathways >> Cell Cycle/DNA Damage >> DNA/RNA Synthesis
Research Areas >> Others

[References]

[1]. Dohno C, et, al. Amphiphilic DNA Duplex Stabilized by a Hydrophobic Zipper. European Journal of Organic Chemistry. September 2012. 27: 5317-5323.

Chemical & Physical Properties

[ Molecular Formula ]:
C32H33N3O7

[ Molecular Weight ]:
571.62000

[ Exact Mass ]:
571.23200

[ PSA ]:
121.14000

[ LogP ]:
3.94900

[ Storage condition ]:
Store dry at 2-8°C

Synthetic Route


Related Compounds

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