4,6-Dichloro-5-pyrimidinamine
Suppliers
Names
[ CAS No. ]:
5413-85-4
[ Name ]:
4,6-Dichloro-5-pyrimidinamine
[Synonym ]:
4,6-dichloro-5-pyrimidinamin
5-AMINO-4,6-DICHLOROPYFIMIDINE
Pyrimidine, 5-amino-4,6-dichloro-
5-Amino-4,6-dichloro
5-Pyrimidinamine, 4,6-dichloro-
4,6-Dichloro-5-aminopyrimidine
5-Amino-4,6-dichloropyrimidine
4,6-Dichloro-5-pyrimidinamine
4,6-dichloropyrimidin-5-amine
5-AMino-4
4,6-dichloropyrimidine-5-amine
MFCD00006108
5-amino-4,6-dichloropyrimididne
EINECS 226-503-7
5-amino-4,6-dichloro-pyrimidine
5-amino-4,6-dichloro-4-pyrimidine
Chemical & Physical Properties
[ Density]:
1.6±0.1 g/cm3
[ Boiling Point ]:
267.1±35.0 °C at 760 mmHg
[ Melting Point ]:
145-148 °C(lit.)
[ Molecular Formula ]:
C4H3Cl2N3
[ Molecular Weight ]:
163.99
[ Flash Point ]:
115.3±25.9 °C
[ Exact Mass ]:
162.970398
[ PSA ]:
51.80000
[ LogP ]:
1.81
[ Vapour Pressure ]:
0.0±0.5 mmHg at 25°C
[ Index of Refraction ]:
1.633
[ Storage condition ]:
2-8°C
[ Water Solubility ]:
slightly soluble
MSDS
Safety Information
[ Symbol ]:
GHS07
[ Signal Word ]:
Warning
[ Hazard Statements ]:
H315-H319-H335
[ Precautionary Statements ]:
P261-P305 + P351 + P338
[ Personal Protective Equipment ]:
dust mask type N95 (US);Eyeshields;Gloves
[ Hazard Codes ]:
Xi: Irritant;
[ Risk Phrases ]:
R36/37/38
[ Safety Phrases ]:
S26-S36-S24/25
[ RIDADR ]:
NONH for all modes of transport
[ WGK Germany ]:
3
[ HS Code ]:
29335995
Synthetic Route
Precursor & DownStream
Precursor
DownStream
Customs
[ HS Code ]: 2933599090
[ Summary ]:
2933599090. other compounds containing a pyrimidine ring (whether or not hydrogenated) or piperazine ring in the structure. VAT:17.0%. Tax rebate rate:13.0%. . MFN tariff:6.5%. General tariff:20.0%
Articles
J. Med. Chem. 31(3) , 606-12, (1988)
Several 9-alkyl-6-substituted-purines were synthesized and tested for anticonvulsant activity against maximal electroshock-induced seizures (MES) in rats. Most compounds were prepared in three steps f...
J. Comb. Chem. 8(3) , 410-6, (2006)
A regiospecific strategy for the preparation of N(7)-substituted purines in an efficient manner was devised. This approach to 6,7,8-trisubstituted purines relies on the cyclization reactions of suitab...
J. Med. Chem. 35(22) , 4180-4, (1992)
The synthesis of various chiral derivatives of (+)-erythro-9-(2-hydroxy-3-nonyl)adenine, (+)-EHNA, from (2S,3R)-3-amino-1,2-O-isopropylidene-1,2-nonanediol by condensation with 5-amino-4,6-dichloropyr...