ChemicalBook > CAS DataBase List > 2-Aminoadenosine

2-Aminoadenosine

Product Name
2-Aminoadenosine
CAS No.
2096-10-8
Chemical Name
2-Aminoadenosine
Synonyms
2-NH2-A;Aminoadenosine;2-AMINE ADENOSINE;2,6-DIAMINOPURINE RIBOSIDE;0/8/96;2-NH2-Ar;NSC 7363;2-NH2-rA;2-NH?-rA;2-AMinoadenosin
CBNumber
CB2468756
Molecular Formula
C10H14N6O4
Formula Weight
282.26
MOL File
2096-10-8.mol
More
Less

2-Aminoadenosine Property

Melting point:
241-243°C (dec.)
storage temp. 
Keep in dark place,Sealed in dry,Room Temperature
solubility 
Aqueous Acid (Slightly, Heated, Sonicated), DMSO (Slightly, Sonicated), Ethanol
form 
Powder
Boiling point:
798.5±70.0 °C(Predicted)
Density 
2.25±0.1 g/cm3(Predicted)
pka
13.10±0.70(Predicted)
color 
White to Off-White
InChIKey
ZDTFMPXQUSBYRL-UUOKFMHZSA-N
CAS DataBase Reference
2096-10-8(CAS DataBase Reference)
More
Less

Safety

Safety Statements 
24/25
HS Code 
29389090
More
Less

Hazard and Precautionary Statements (GHS)

Symbol(GHS)
Signal word
Warning
Hazard statements

H315Causes skin irritation

H319Causes serious eye irritation

Precautionary statements

P264Wash hands thoroughly after handling.

P264Wash skin thouroughly after handling.

P280Wear protective gloves/protective clothing/eye protection/face protection.

More
Less

N-Bromosuccinimide Price

TCI Chemical
Product number
A2135
Product name
2-Aminoadenosine
Purity
>98.0%(HPLC)(T)
Packaging
5g
Price
$48
Updated
2024/03/01
TCI Chemical
Product number
A2135
Product name
2-Aminoadenosine
Purity
>98.0%(HPLC)(T)
Packaging
25g
Price
$236
Updated
2024/03/01
Alfa Aesar
Product number
044748
Product name
2-Aminoadenosine, 97%
Packaging
1g
Price
$46.65
Updated
2024/03/01
Alfa Aesar
Product number
044748
Product name
2-Aminoadenosine, 97%
Packaging
5g
Price
$163.65
Updated
2024/03/01
Alfa Aesar
Product number
044748
Product name
2-Aminoadenosine, 97%
Packaging
25g
Price
$549.65
Updated
2024/03/01
More
Less

2-Aminoadenosine Chemical Properties,Usage,Production

Description

2-Aminoadenosine is a known analogue of adenosine that engages in three hydrogen bonds of the W-C type, adding considerable stability to the double helix.

Chemical Properties

White Powder

Uses

2-Aminoadenosine is a nucleoside analog as inhibitor or substrate of adenosine kinase from M. tuberculosis. It is also used to synthesize 2′-O-methyl and 3′-O-methyl Guanosine.

Definition

ChEBI: 2-Aminoadenosine is a purine nucleoside.

Synthesis

The synthesis of 2-aminoadenosine (2-AA): Assays were performed in 5 and 10% of aprotic dipolar co-solvents, at 60°C, twelve units/ml cell lysate were added to 150 ml of a solution kept thermostatically at 60 °C, and having the following composition of substrate solutions: 15mM Uridine/2 ' -Deoxyuridine,5 mM 2,6-Diaminopurine, and 30 mM potassium phosphate buffer, pH 7. After 5 hours, the reaction mixture was filtered by centrifugation at 2000 x g for 30 min, at 4°C, through an Amicon ultra-4 Centrifugal Filter Devices (Millipore, Bedford, MA) with a 3000-Da cutoff, and the filtrate was recovered.

References

Pyrazolo[3,4-d]pyrimidine ribonucleosides related to 2-aminoadenosine and isoguanosine: synthesis, deamination and tautomerism. DOI: 10.1039/B708736E
An Efficient Process for Synthesis of 2′-O-methyl and 3′-O-methyl Guanosine from 2-aminoadenosine Using Diazomethane and the Catalyst Stannous Chloride. DOI: 10.1080/15257770500544529

2-Aminoadenosine Preparation Products And Raw materials

Raw materials

Preparation Products

More
Less

2-Aminoadenosine Suppliers

Carbosynth
Tel
--
Fax
--
Email
sales@carbosynth.com
Country
United Kingdom
ProdList
6005
Advantage
58
Carbosynth Limited
Tel
--
Fax
--
Email
sales@carbosynth.com
Country
United Kingdom
ProdList
6581
Advantage
61
Leancare Ltd.
Tel
--
Fax
--
Email
enquiry@leancare.co.uk
Country
United Kingdom
ProdList
6446
Advantage
42
MOLEKULA Ltd.
Tel
--
Fax
--
Email
kevinbanks@molekula.com
Country
United Kingdom
ProdList
6140
Advantage
66
CARBONE SCIENTIFIC CO.,LTD
Tel
--
Fax
--
Email
sales@carbonesci.com
Country
United Kingdom
ProdList
6666
Advantage
30
UK GREEN SCIENTIFIC CO.,LIMITED
Tel
--
Fax
--
Email
sales@gs-chem.com
Country
United Kingdom
ProdList
6098
Advantage
47
Eurolabs Limited
Tel
--
Fax
--
Country
United Kingdom
ProdList
6309
Advantage
46
Apin Chemicals Ltd.
Tel
--
Fax
--
Email
info@apinchemicals.com
Country
United Kingdom
ProdList
6807
Advantage
42
More
Less

View Lastest Price from 2-Aminoadenosine manufacturers

Xinxiang Aurora Biotechnology Co.,Ltd.
Product
2,6-Diaminopurine-riboside 2096-10-8
Price
US $0.00-0.00/Kg
Min. Order
1Kg
Purity
98%
Supply Ability
20Ton
Release date
2024-10-31
Xinxiang Aurora Biotechnology Co.,Ltd.
Product
2-Aminoadenosine 2096-10-8
Price
US $0.00-0.00/Kg
Min. Order
1Kg
Purity
98%
Supply Ability
20Ton
Release date
2024-10-31
WUHAN FORTUNA CHEMICAL CO., LTD
Product
2-Aminoadenosine 2096-10-8
Price
US $0.00-0.00/Kg/Drum
Min. Order
1KG
Purity
98%min
Supply Ability
1000KGS
Release date
2021-11-17

2096-10-8, 2-Aminoadenosine Related Search:


  • 2-AMINE ADENOSINE
  • 2-AMINOADENOSINE
  • 2,6-DIAMINOPURINE RIBOSIDE
  • 2-AMINOADENOSINE HPLC98+%
  • Aminoadenosine
  • 2-NH2-A
  • Adenosine, 2-amino-
  • Regadenoson Impurity 23
  • (2R,3R,4S,5R)-2-(2,6-Diaminopurin-9-yl)-5-(hydroxymethyl)oxolane-3,4-diol
  • 2-AMinoadenosin
  • 2-NH2-Ar
  • 2-Aminoadenosine≥ 99% (HPLC)
  • 2,6-DiaMino-9-β-D-ribofuranosyl-9H-purine
  • 2,6-DiaMinonebularine
  • 2,6-DiaMinopurinosine
  • 9-β-Ribosyl-2,6-diaMinopurine
  • NSC 7363
  • 2,6-Diamino-9-(beta-D-ribofuranosyl)purine 2,6-Diaminopurine Riboside
  • 2, 6-Diaminopurine-riboside / 2-amino-adenosine
  • 9H-Purine-2,6-diamine, 9-.β.-D-ribofuranosyl-
  • 2-aminoadenine nucleoside
  • 2-Aminoadenosine &gt
  • 2,6-Diamino-9-(beta-D-ribofuranosyl)purine
  • 2-Aminoadenosine USP/EP/BP
  • TIANFU CHEM 2-Aminoadenosine
  • 2-NH2-rA
  • 0/8/96
  • (2R,3R,4S,5R)-2-(2,6-Diamino-9H-purin-9-yl)-5-(hydroxymethyl)tetrahydrofuran-3,4-diol
  • 2-NH?-rA
  • Regadenoson Impurity U18
  • Regadson Impurity 18
  • 2096-10-8
  • 96-10-8
  • 2090-10-8
  • C10H14N6O4
  • Amines
  • Heterocycles
  • Nucleotides and Nucleosides
  • Nucleic acids
  • Bases & Related Reagents
  • Nucleotides
  • 2096-10-8
  • Nucleosides-Ribonucleosides