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Name	6-Chloro-9-(2-C-methyl-beta-D-ribofuranosyl)-9H-purine	EINECS	N/A
CAS No.	205171-05-7	Density	1.86 g/cm³
PSA	113.52000	LogP	-0.51870
Solubility	N/A	Melting Point	N/A
Formula	C₁₁H₁₃ClN₄O₄	Boiling Point	590.081 °C at 760 mmHg
Molecular Weight	300.702	Flash Point	310.67 °C
Transport Information	N/A	Appearance	N/A
Safety		Risk Codes	N/A
Molecular Structure		Hazard Symbols	N/A
Synonyms	6-CHLORO-9-(2-METHYL-BETA-D-RIBOFURANOSYL)-9H-PURINE;6-Chloro-9-(2-C-methyl-beta-D-ribofuranosyl)-9H-purine;6-Chloro-9-(2-C-Methyl-β-D-ribofuranosyl)-9H-purine;(2R,3R,4R,5R)-2-(6-Chloro-9H-purin-9-yl)-5-(hydroxyMethyl)-3-Methyltetrahydrofuran-3,4-diol

6-Chloro-9-(2-C-methyl-beta-D-ribofuranosyl)-9H-purine Specification

The CAS registry number of 6-Chloro-9-(2-C-methyl-beta-D-ribofuranosyl)-9H-purine is 205171-05-7. It is also named as 9H-purine, 6-chloro-9-(2-C-methyl-beta-D-ribofuranosyl)- . 6-Chloro-9-(2-C-methyl-beta-D-ribofuranosyl)-9H-purine is a kind of purine. Purines, including substituted purines and their tautomers, are the most widely distributed kind of nitrogen-containing heterocycle in nature. Aside from DNA and RNA, purines are biochemically significant components in a number of other important biomolecules, such as ATP, GTP, cyclic AMP, NADH, and coenzyme A. Purine itself, has not been found in nature, but it can be produced by organic synthesis.

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