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| 4-Chloro-2,6-diaminopyrimidine Basic information |
Product Name: | 4-Chloro-2,6-diaminopyrimidine | Synonyms: | 4-DiaMino-6-chloropyriMidine;NSC 8818;DIAMINO-6-CHLOROPYRIMIDINE, 2,4-(SH);2,4-DIAMINO-6-CHLOROPYRIMIDINE FOR SYNTH;2,6-DiaMino-4-chloropyriMidine 98%;DiaMino-6-chloropyriMid;2,4-Diamino-6-chloropyrimidine,98%;4-Chloro-2,6-diaminopyrimidine, 4-Chloro-2,6-diamino-1,3-diazine | CAS: | 156-83-2 | MF: | C4H5ClN4 | MW: | 144.56 | EINECS: | 205-863-9 | Product Categories: | Bases & Related Reagents;Heterocycles;Nucleotides;Heterocyclic Compounds;Pyrimidines;PYRIMIDINE;Pyridines, Pyrimidines, Purines and Pteredines;Heterocycle-Pyrimidine series;bc0001;156-83-2;john's;ADVANCED INT. | Mol File: | 156-83-2.mol | |
| 4-Chloro-2,6-diaminopyrimidine Chemical Properties |
Melting point | 199-202 °C(lit.) | Boiling point | 199-202 °C | density | 1.3966 (rough estimate) | vapor pressure | 0.0±1.1 mmHg at 25°C | refractive index | 1.702 | Fp | 218.9±29.6 °C | storage temp. | Keep in dark place,Sealed in dry,Room Temperature | solubility | slightly soluble | pka | 3.66±0.10(Predicted) | form | Solid | color | White to Pale Yellow | Water Solubility | slightly soluble | BRN | 118455 | InChI | InChI=1S/C4H5ClN4/c5-2-1-3(6)9-4(7)8-2/h1H,(H4,6,7,8,9) | InChIKey | QJIUMVUZDYPQRT-UHFFFAOYSA-N | SMILES | C1(N)=NC(Cl)=CC(N)=N1 | CAS DataBase Reference | 156-83-2(CAS DataBase Reference) | NIST Chemistry Reference | Pyrimidine, 6-chloro-2,4-diamino-(156-83-2) |
Hazard Codes | Xn,Xi | Risk Statements | 22-36/37/38 | Safety Statements | 26-24/25 | WGK Germany | 3 | Hazard Note | Irritant | HS Code | 29335995 |
| 4-Chloro-2,6-diaminopyrimidine Usage And Synthesis |
Chemical Properties | White Cyrstalline Solid | Uses | Melamine and Related Compounds in Dog Food Using GC-MS | Definition |
ChEBI: 6-chloro-2,4-pyrimidinediamine (4-Chloro-2,6-diaminopyrimidine) is a member of pyrimidines and an organohalogen compound.
| Synthesis |
2,4-Diamino-6-hydroxypyrimidine (1.00 g, 7.93 mmol) was added to POCl3 (9 mL) and stirred at 97 ℃ for 17 h. The reaction solution was added to ice water slowly and then stirred at 90 C for 1 h. The pH of this solution was adjusted to 8 with NaOH, and then it was extracted with EtOAC (150 mL 3). The combined organic layers were dried with Na2SO4, filtered, and concentrated to give white solid 4-Chloro-2,6-diaminopyrimidine 0.97 g, yielding 85%.
| Purification Methods | It recrystallises from boiling H2O (charcoal) as needles; it also crystallises from Me2CO. [Büttner Chem Ber 36 2232 1903, Roth J Am Chem Soc 72 1914 1950, UV: Brown & Jacobsen J Chem Soc 3172 1962, Beilstein 24 H 318, 25 III/IV 2788.] |
| 4-Chloro-2,6-diaminopyrimidine Preparation Products And Raw materials |
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