Guanosine,2'-deoxy-

The Deoxyguanosine, with the CAS registry number 961-07-9 and EINECS registry number 213-505-8, has the IUPAC name of 2'-deoxyguanosine. And the molecular formula of this chemical is C₁₀H₁₃N₅O₄. It is a derivative of the nucleoside adenosine, and belongs to the product categories: Pyridines, Pyrimidines, Purines and Pteredines; Nucleotides and Nucleic Acids. What's more, it is used in the biochemical study.

The Deoxyguanosine is composed of the purine nucleoside guanine linked by its N9 nitrogen to the C1 carbon of deoxyribose. It is similar to guanosine, but with one hydroxyl group removed from the 2' position of the ribose sugar (making it deoxyribose). If a phosphate group is attached at the 5' position, it becomes deoxyguanosine monophosphate.

The physical properties of Deoxyguanosine are as following: (1)# of Rule of 5 Violations: 1; (2)ACD/BCF (pH 5.5): 1; (3)ACD/BCF (pH 7.4): 1; (4)ACD/KOC (pH 5.5): 5.662; (5)ACD/KOC (pH 7.4): 5.687; (6)#H bond acceptors: 9; (7)#H bond donors: 5; (8)#Freely Rotating Bonds: 4; (9)Polar Surface Area: 134.99 Å²; (10)Index of Refraction: 1.907; (11)Molar Refractivity: 59.959 cm³; (12)Molar Volume: 128.164 cm³; (13)Polarizability: 23.77×10^-24cm³; (14)Surface Tension: 107.624 dyne/cm; (15)Density: 2.085 g/cm³; (16)Flash Point: 392.553 °C; (17)Enthalpy of Vaporization: 111.206 kJ/mol; (18)Boiling Point: 725.475 °C at 760 mmHg; (19)Vapour Pressure: 0 mmHg at 25°C.

Uses of Deoxyguanosine: It can react with 2,2-diethoxy-1-methyl-pyrrolidine to produce 2-N-(N-methylpyrrolidin-2-ylidene)-2'-deoxyguanosine. This reaction will need solvent ethanol. The reaction time is 48 hours, and the yield is about 85%.

You can still convert the following datas into molecular structure:
(1)SMILES: c1nc2c(n1[C@H]3C[C@@H]([C@H](O3)CO)O)[nH]c(nc2=O)N
(2)InChI: InChI=1/C10H13N5O4/c11-10-13-8-7(9(18)14-10)12-3-15(8)6-1-4(17)5(2-16)19-6/h3-6,16-17H,1-2H2,(H3,11,13,14,18)/t4-,5+,6+/m0/s1
(3)InChIKey: YKBGVTZYEHREMT-KVQBGUIXBI