<Suppliers Price>

4,6-Dichloro-5-pyrimidinamine

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

Biological Activity

[Description]:

4,6-Dichloropyrimidin-5-amine is a biochemical reagent that can be used as a biological material or organic compound for life science related research.

[Related Catalog]:

Research Areas >> Others
Signaling Pathways >> Others >> Others

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

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

6-(Alkylamino)-9-benzyl-9H-purines. A new class of anticonvulsant agents.

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...

An efficient and regiospecific strategy to N7-substituted purines and its application to a library of trisubstituted purines.

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...

Adenosine deaminase inhibitors. Synthesis and biological evaluation of C1' and nor-C1' derivatives of (+)-erythro-9-(2(S)-hydroxy-3(R)-nonyl)adenine.

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...


More Articles


Related Compounds

The content on this webpage is sourced from various professional data sources. If you have any questions or concerns regarding the content, please feel free to contact service1@chemsrc.com.