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4-Chloro-2,6-diaminopyrimidine

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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
  • PYRIMIDINE
  • Heterocyclic Compounds
  • Pyrimidines
  • Nucleotides
  • Pyridines, Pyrimidines, Purines and Pteredines
  • Heterocycle-Pyrimidine series
  • bc0001
  • 156-83-2
  • john's
  • ADVANCED INT.
Mol File:
156-83-2.mol
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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
Flash point:
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)
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Safety Information

Hazard Codes 
Xn,Xi
Risk Statements 
22-36/37/38
Safety Statements 
26-24/25
WGK Germany 
3
Hazard Note 
Irritant
HS Code 
29335995

MSDS

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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

Raw materials

4-Chloro-2,6-diaminopyrimidineSupplier

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