CAS 2545-26-8

6-Iodo-9H-purine

Description:

6-Iodo-9H-purine, with the CAS number 2545-26-8, is a purine derivative characterized by the presence of an iodine atom at the 6-position of the purine ring. This compound exhibits properties typical of purines, including being a heterocyclic aromatic organic compound. It is generally soluble in polar solvents, which is common for purine derivatives, and may exhibit moderate stability under standard conditions. The presence of the iodine substituent can influence its reactivity, making it a potential candidate for various chemical reactions, including nucleophilic substitutions. 6-Iodo-9H-purine can serve as an important intermediate in the synthesis of nucleosides and nucleotides, which are vital in biochemistry and molecular biology. Additionally, its structural similarity to adenine and guanine allows it to participate in biological processes, potentially affecting nucleic acid metabolism. As with many halogenated compounds, safety precautions should be taken when handling it due to potential toxicity and environmental impact.

Formula: C₅H₃IN₄

InChI: InChI=1S/C5H3IN4/c6-4-3-5(9-1-7-3)10-2-8-4/h1-2H,(H,7,8,9,10)

InChI key: InChIKey=NIBFSSALYRLHPY-UHFFFAOYSA-N

SMILES: IC1=C2C(=NC=N1)N=CN2

Synonyms:

• 1H-Purine, 6-iodo-
• 1H-Purine, 6-iodo- (9CI)
• 1H-Purine, 6-iodo-, hemihydrate
• 6-Iodo-9H-purine
• 6-iodo-5H-purine
• 6-iodo-7H-purine
• 9H-Purine, 6-iodo-
• Ai3-50271
• Nsc 25803
• Purine, 6-iodo-
• 6-Iodopurine

6-Iodo-7H-purine

CAS: 2545-26-8

Formula: C₅H₃IN₄

Purity: 95%

Color and Shape: Solid

Molecular weight: 246.0086

Ref: IN-DA006UCW

6-Iodo-7H-purine

CAS: 2545-26-8

6-Iodo-7H-purine

Formula: C₅H₃IN₄

Purity: 95%

Color and Shape: off white to faint yellow to grey powder

Molecular weight: 246.01g/mol

Ref: 54-OR48101

6-Iodopurine

CAS: 2545-26-8

6-Iodopurine is a biologically active substance that belongs to the group of carbinols. It is biosynthesized from 6-chloropurine and an iridoid glucoside, and has been shown to have biochemical properties. 6-Iodopurine can be converted into 6-iodoindoxyl by oxidation with halogens or transfer mechanism with palladium-catalyzed cross-coupling. A high efficiency method for the synthesis of this substance has been developed using a strain of bacteria. The reaction requires an activation energy of 150 kJ/mol.br>
6-Iodopurine inhibits tumor growth by inhibiting DNA synthesis. It also possesses anti-inflammatory activity, which may be due to its inhibitory effects on prostaglandin synthesis.

Formula: C₅H₃IN₄

Purity: Min. 95%

Color and Shape: White Powder

Molecular weight: 246.01 g/mol

Ref: 3D-FI02692

6-iodo-7H-purine

CAS: 2545-26-8

Purity: 98%

Molecular weight: 246.0110016

Ref: 10-F772271