2,6-Diaminopurine
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2,6-Diaminopurine
structure -
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CAS No:
1904-98-9
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Formula:
C5H6N6
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Chemical Name:
2,6-Diaminopurine
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Synonyms:
9H-Purine-2,6-diamine;Purine,2,6-diamino-;1H-Purine-2,6-diamine;2,6-Diaminopurine;2-Aminoadenine;SQ 21065;NSC 743;1006-52-6;39001-24-6
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CAS No:
Description
white to light yellow crystal powderChEBI: A member of the class of 2,6-diaminopurines that is 9H-purine in which the hydrogens at positions 2 and 6 are replaced by amino groups.
9H-purine-2,6-diamine is a member of the class of 2,6-diaminopurines that is 9H-purine in which the hydrogens at positions 2 and 6 are replaced by amino groups. It has a role as an antineoplastic agent. It is a primary amino compound and a member of 2,6-diaminopurines. It derives from an adenine.|2,6-Diaminopurine is one of a number of organic compounds that share a similar purine structure and possess antiviral and antitumor properties. 2,6-Diaminopurine nucleosides are versatile synthetic precursors for specific N-6 modifications of antiviral and antitumor agents. (NCI04)
2,6-Diaminopurine Basic Attributes
150.14
150.14
9624
205-507-2
49P95BAU4Z
743
DTXSID0062052
C29796
29335990
Characteristics
107
-0.9
White to light yellow Crystalline Powder or Granules
1.2562 (rough estimate)
302 °C
285 °C(lit.)
155 °C
1.8750 (estimate)
2.38 g/L (20 ºC)
Store in a cool, dry place. Store in a tightly closed container.
3.65E-05mmHg at 25°C
Safety Information
NONH for all modes of transport
3
22-36/37/38-40-20/21/22
26-45-36/37-36/37/39-27-36-22
US7570000
Xn
Stable under normal temperatures and pressures.
P261-P280-P305 + P351 + P338
H302 + H312 + H332-H315-H319-H335-H351
|Warning|H302 (87.76%): Harmful if swallowed [Warning Acute toxicity, oral]|P201, P202, P261, P264, P270, P271, P280, P281, P301+P312, P302+P352, P304+P312, P304+P340, P305+P351+P338, P308+P313, P312, P321, P322, P330, P332+P313, P337+P313, P362, P363, P403+P233, P405, and P501|Aggregated GHS information provided by 49 companies from 8 notifications to the ECHA C&L Inventory. Each notification may be associated with multiple companies.
Drug Information
Compounds that inhibit cell production of DNA or RNA. (See all compounds classified as Nucleic Acid Synthesis Inhibitors.)
2,6-diaminopurine
2,6-Diaminopurine Use and Manufacturing
Used as an intermediate in organic synthesis
9H-Purine-2,6-diamine: ACTIVE
Computed Properties
Molecular Weight:150.14
XLogP3:-0.9
Hydrogen Bond Donor Count:3
Hydrogen Bond Acceptor Count:5
Exact Mass:150.06539422
Monoisotopic Mass:150.06539422
Topological Polar Surface Area:107
Heavy Atom Count:11
Complexity:150
Covalently-Bonded Unit Count:1
Compound Is Canonicalized:Yes
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