1. Home
  2. 8H-Purin-8-one, 6-amino-1,7-dihydro-

Contact Angene

Tel: +852 8191 6999

Email: [email protected]

Brc1cnc(nc1)C
Pyrimidine, 5-bromo-2-methyl-
CCCP1(=O)OP(=O)(CCC)OP(=O)(O1)CCC
1,3,5,2,4,6-Trioxatriphosphorinane, 2,4,6-tripropyl-, 2,4,6-trioxide
CC1(C)OB(OC1(C)C)B1OC(C(O1)(C)C)(C)C
2,2'-Bi-1,3,2-dioxaborolane, 4,4,4',4',5,5,5',5'-octamethyl-
O=C(C=Cc1ccccc1)C=Cc1ccccc1.O=C(C=Cc1ccccc1)C=Cc1ccccc1.O=C(C=Cc1ccccc1)C=Cc1ccccc1.[Pd].[Pd]
Tris(dibenzylideneacetone)dipalladium
C1CCC(CC1)P(C1CCCCC1)C1CCCCC1.Cc1cc(C)c(c(c1)C)N1CCN(C1=[Ru](=Cc1ccccc1)(Cl)Cl)c1c(C)cc(cc1C)C
Ruthenium,[1,3-bis(2,4,6-trimethylphenyl)-2-imidazolidinylidene]dichloro(phenylmethylene)(tricyclohexylphosphine)-, (SP-5-41)-

8H-Purin-8-one, 6-amino-1,7-dihydro-

Oc1nc2c([nH]1)c(N)ncn2 Request for Quotation
Chemical Name: 8H-Purin-8-one, 6-amino-1,7-dihydro-
CAS Number: 21149-26-8
Product Number: AG006Z3K(AGN-PC-0O7TMV)
Synonyms:
MDL No:
Molecular Formula: C5H5N5O
Molecular Weight: 151.1261

Identification/Properties

Computed Properties
Molecular Weight:
151.129g/mol
XLogP3:
-1.2
Hydrogen Bond Donor Count:
3
Hydrogen Bond Acceptor Count:
4
Rotatable Bond Count:
0
Exact Mass:
151.049g/mol
Monoisotopic Mass:
151.049g/mol
Topological Polar Surface Area:
92.9A^2
Heavy Atom Count:
11
Formal Charge:
0
Complexity:
184
Isotope Atom Count:
0
Defined Atom Stereocenter Count:
0
Undefined Atom Stereocenter Count:
0
Defined Bond Stereocenter Count:
0
Undefined Bond Stereocenter Count:
0
Covalently-Bonded Unit Count:
1
Compound Is Canonicalized:
Yes

Safety Information

GHS Pictogram:
Signal Word:
Warning
UN#:
N/A
Hazard Statements:
H302-H315-H319-H335
Precautionary Statements:
P261-P305+P351+P338
Class:
N/A
Packing Group:
N/A

NMR Spectrum

Other Analytical Data

Request for Quotation

Customer Feedback

Chemical Structure


6-Amino-7H-purin-8-ol, also known as adenine, is a versatile compound widely used in chemical synthesis. Its primary application lies in serving as a fundamental building block in the production of nucleotides, which are essential components of DNA and RNA. By incorporating 6-Amino-7H-purin-8-ol into synthetic reactions, chemists are able to generate various nucleosides and nucleotides through controlled chemical processes. This valuable compound plays a crucial role in the development of pharmaceuticals, agrochemicals, and materials with specialized functions, making it a cornerstone in organic synthesis research.