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1445-39-2

1445-39-2 Structure

1445-39-2 Structure
IdentificationMore
[Name]

2-AMINO-5-IODOPYRIMIDINE
[CAS]

1445-39-2
[Synonyms]

2-AMINO-5-IODOPYRIMIDINE
5-Iodo-2-pyrimidinamine
[EINECS(EC#)]

625-750-1
[Molecular Formula]

C4H4IN3
[MDL Number]

MFCD01075666
[Molecular Weight]

221
[MOL File]

1445-39-2.mol
Chemical PropertiesBack Directory
[Appearance]

cream to brown crystalline powder
[Melting point ]

219 °C
[Boiling point ]

364.9±34.0 °C(Predicted)
[density ]

2.204±0.06 g/cm3(Predicted)
[storage temp. ]

Keep in dark place,Sealed in dry,Room Temperature
[form ]

powder
[pka]

2.08±0.10(Predicted)
[Sensitive ]

Light Sensitive
[InChI]

InChI=1S/C4H4IN3/c5-3-1-7-4(6)8-2-3/h1-2H,(H2,6,7,8)
[InChIKey]

HAFKCGZQRIIADX-UHFFFAOYSA-N
[SMILES]

C1(N)=NC=C(I)C=N1
[CAS DataBase Reference]

1445-39-2(CAS DataBase Reference)
Safety DataBack Directory
[Hazard Codes ]

Xi
[Risk Statements ]

R36/37/38:Irritating to eyes, respiratory system and skin .
R41:Risk of serious damage to eyes.
R37/38:Irritating to respiratory system and skin .
R22:Harmful if swallowed.
[Safety Statements ]

S37/39:Wear suitable gloves and eye/face protection .
S26:In case of contact with eyes, rinse immediately with plenty of water and seek medical advice .
S39:Wear eye/face protection .
[WGK Germany ]

3
[HS Code ]

2933599590
[Storage Class]

11 - Combustible Solids
[Hazard Classifications]

Acute Tox. 4 Oral
Eye Dam. 1
Skin Irrit. 2
STOT SE 3
Hazard InformationBack Directory
[Chemical Properties]

cream to brown crystalline powder
[Uses]

2-Amino-5-iodopyrimidine is used as a reactant in the synthesis of aminopyrimidine and cyclic guanidine amino acids.
[Synthesis]

2-Aminopyrimidine

109-12-6

2-AMINO-5-IODOPYRIMIDINE

1445-39-2

General procedure for the synthesis of 2-amino-5-iodopyrimidine from 2-aminopyrimidine: a mixture of 2-aminopyrimidine (2.4 g, 25 mmol, 1.0 eq.) and elemental iodine (2.7 g, 10.7 mmol, 0.43 eq.) was dissolved in 60 mL of glacial acetic acid, followed by the addition of periodate (0.86 g, 3.76 mmol, 0.15 eq.) and 0.5 mL of concentrated sulfuric acid dissolved in 3 mL of water. The reaction mixture was heated to 80 °C and maintained for 24 h under nitrogen protection. Upon completion of the reaction, the reaction mixture was poured into saturated aqueous sodium thiosulfate solution until the solution was clarified (200 mL each time for 3 times) and then extracted with dichloromethane. The organic phases were combined, dried with anhydrous sodium sulfate, filtered and concentrated under reduced pressure. Purification by silica gel column chromatography afforded 2-amino-5-iodopyrimidine (1.4 g, 22.2% yield) as a white solid.

[References]

[1] Heterocycles, 1984, vol. 22, # 5, p. 1195 - 1210
[2] Journal of Organic Chemistry, 2000, vol. 65, # 22, p. 7468 - 7474
[3] Journal of Organic Chemistry, 2008, vol. 73, # 23, p. 9326 - 9333
[4] Synthesis, 1984, # 3, p. 252 - 254
[5] Patent: CN105622638, 2016, A. Location in patent: Paragraph 0362
Spectrum DetailBack Directory
[Spectrum Detail]

2-AMINO-5-IODOPYRIMIDINE(1445-39-2)1HNMR
Well-known Reagent Company Product InformationBack Directory
[Alfa Aesar]

2-Amino-5-iodopyrimidine, 97%(1445-39-2)
[Sigma Aldrich]

1445-39-2(sigmaaldrich)
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