6-Amino-7-deazapurine - CAS 1500-85-2
Catalog: |
BB010483 |
Product Name: |
6-Amino-7-deazapurine |
CAS: |
1500-85-2 |
Synonyms: |
4-Amino-7H-pyrrolo[2,3-d]pyrimidine; 7-Deazaadenine; 4-Aminopyrrolo(2,3-d)pyrimidine; 1H-Pyrrolo[2,3-d]pyrimidin-4-amine; 7H-Pyrrolo[2,3-d]pyrimidin-4-ylamine |
IUPAC Name: | 7H-pyrrolo[2,3-d]pyrimidin-4-amine |
Description: | 6-Amino-7-deazapurine (CAS# 1500-85-2) is a useful research chemical. |
Molecular Weight: | 134.14 |
Molecular Formula: | C6H6N4 |
Canonical SMILES: | C1=CNC2=C1C(=NC=N2)N |
InChI: | InChI=1S/C6H6N4/c7-5-4-1-2-8-6(4)10-3-9-5/h1-3H,(H3,7,8,9,10) |
InChI Key: | PEHVGBZKEYRQSX-UHFFFAOYSA-N |
Boiling Point: | 318.3±45.0°C (Predicted) |
Melting Point: | 257-262°C |
Purity: | 97.0 % |
Density: | 1.61±0.1 g/cm3 (Predicted) |
Appearance: | White to Pale Brown Solid |
Storage: | Store at 2-8°C |
MDL: | MFCD01686848 |
LogP: | 1.12130 |
GHS Hazard Statement: | H301 (93.02%): Toxic if swallowed [Danger Acute toxicity, oral] |
Precautionary Statement: | P264, P270, P301+P310, P321, P330, P405, and P501 |
Signal Word: | Danger |
Publication Number | Title | Priority Date |
US-2021189495-A1 | Adenylate Cyclase 7 (ADCY7) Variants And Uses Thereof | 20191222 |
WO-2021122944-A1 | Compositions and methods for treating retinitis pigmentosa | 20191218 |
WO-2021123074-A1 | Methods of sequencing by synthesis using a consecutive labeling scheme | 20191218 |
WO-2021119594-A1 | Reducing antibiotic resistance in bacteria using pro-active genetics | 20191213 |
WO-2021119402-A1 | Compositions and methods for light-directed biomolecular barcoding | 20191212 |
PMID | Publication Date | Title | Journal |
28628181 | 20170705 | Synthesis and antiviral evaluation of base-modified deoxythreosyl nucleoside phosphonates | Organic & biomolecular chemistry |
23606629 | 20130601 | Synthesis and anti-herpetic activity of phosphoramidate ProTides | ChemMedChem |
22690148 | 20120401 | First total synthesis of a naturally occurring iodinated 5'-deoxyxylofuranosyl marine nucleoside | Marine drugs |
22173724 | 20120116 | Influence of the nucleobase and anchimeric assistance of the carboxyl acid groups in the hydrolysis of amino acid nucleoside phosphoramidates | Chemistry (Weinheim an der Bergstrasse, Germany) |
22095665 | 20111209 | Anthraquinone as a redox label for DNA: synthesis, enzymatic incorporation, and electrochemistry of anthraquinone-modified nucleosides, nucleotides, and DNA | Chemistry (Weinheim an der Bergstrasse, Germany) |
Complexity: | 127 |
Compound Is Canonicalized: | Yes |
Covalently-Bonded Unit Count: | 1 |
Defined Atom Stereocenter Count: | 0 |
Defined Bond Stereocenter Count: | 0 |
Exact Mass: | 134.059246208 |
Formal Charge: | 0 |
Heavy Atom Count: | 10 |
Hydrogen Bond Acceptor Count: | 3 |
Hydrogen Bond Donor Count: | 2 |
Isotope Atom Count: | 0 |
Monoisotopic Mass: | 134.059246208 |
Rotatable Bond Count: | 0 |
Topological Polar Surface Area: | 67.6 Å2 |
Undefined Atom Stereocenter Count: | 0 |
Undefined Bond Stereocenter Count: | 0 |
XLogP3: | 0.3 |
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