6-Chloropurine ribonucleoside

6-Chloropurine ribonucleoside
  • CAS No.:2004-06-0
Other grades of this product :
6-Chloropurine ribonucleoside Basic information
Product Name:6-Chloropurine ribonucleoside
Synonyms:6-chloropurineribonucleoside;6-CLPR;6-CHLORO-9-(BETA-D-RIBOFURANOSYL)PURINE;6-CHLOROINOSINE;6-CHLOROPURINE-9-RIBOSIDE;6-CHLOROPURINE NUCLEOSIDE;6-chloro-9-ribofuranosyl-9H-purine;6-Chloropurine riboside, pure, 99+%
CAS:2004-06-0
MF:C10H11ClN4O4
MW:286.67
EINECS:217-904-8
Product Categories:chiral;Biochemistry;Nucleosides and their analogs;Nucleosides, Nucleotides & Related Reagents
Mol File:2004-06-0.mol
6-Chloropurine ribonucleoside Chemical Properties
Melting point 158-162 °C (dec.)(lit.)
Boiling point 614.8±65.0 °C(Predicted)
density 1.7303 (rough estimate)
refractive index -45 ° (C=0.8, H2O)
storage temp. Sealed in dry,Store in freezer, under -20°C
form Powder
pka13.06±0.70(Predicted)
color Yellow to Green
CAS DataBase Reference2004-06-0(CAS DataBase Reference)
Safety Information
Hazard Codes Xi
Risk Statements 36/37/38
Safety Statements 22-24/25-36-26
RTECS UO7520800
10-23
Hazard Note Irritant
HS Code 29389090
MSDS Information
ProviderLanguage
6-Chloropurine riboside English
SigmaAldrich English
ACROS English
6-Chloropurine ribonucleoside Usage And Synthesis
Chemical Propertieswhite to light yellow crystal powde
Uses6-CHLOROPURINE RIBOSIDE acts as a reactant in the synthesis of isozyme-specific enzyme inhibitors as well as in the preparation of dog coronary artery receptor agonists.
Purification MethodsPurify the riboside by suspending the dry solid (~12 g) in hot MeOH (130 mL) and then adding enough hot H2O (~560mL) to cause solution, filter and set aside at 5o overnight. The colourless crystals of the riboside are filtered off, washed with Me2CO, Et2O and dried at 60o/0.1mm. More material can be obtained by evaporating the filtrate to dryness and recrystallisation of the residue from MeOH/H2O (2:1) (15mL/g). It has max 264nm ( 9140) in H2O. [Robins Biochemical Preparations 10 145 1963, Baker et al. J Org Chem 22 954 1957.]

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