4-Chloro-6-methoxypyrimidin-2-amine

Names

[ Name ]:
4-Chloro-6-methoxypyrimidin-2-amine

[Synonym ]:
4-chlor-6-methoxypyrimidin-2-amin
4-methoxy-6-chloro-2-aminopyrimidine
EINECS 410-050-9
MFCD00233535
4-Chloro-6-methoxypyrimidin-2-amine
2-amino-4-chloro-6-methoxypyrimidne
4-chloro-6-methoxypyrimidine-2-ylamine
2-Pyrimidinamine, 4-chloro-6-methoxy-
2-amino-4-methoxy-6-chloropyrimidine
4-Chloro-6-methoxy-2-pyrimidinamine
2-Amino-6-chloro-4-methoxypyrimidine
2-Amino-4-methoxy-6-chloropyri
2-amino-4-chloro-6-methoxypyri
ACMP
2-amino-4-chloro-6-methoxy-pyrimidine
4-chloro-6-methoxy-2-pyrimidinamin
4-chloro-6-methoxy-2-pyrmidylamine
2-AMINO-4-CHLORO-6-METHOXY PYRIMIDINE

Chemical & Physical Properties

[ Density]:
1.4±0.1 g/cm3

[ Boiling Point ]:
349.4±45.0 °C at 760 mmHg

[ Melting Point ]:
168-171 °C(lit.)

[ Molecular Formula ]:
C₅H₆ClN₃O

[ Molecular Weight ]:
159.574

[ Flash Point ]:
165.1±28.7 °C

[ Exact Mass ]:
159.019943

[ PSA ]:
61.03000

[ LogP ]:
1.64

[ Vapour Pressure ]:
0.0±0.8 mmHg at 25°C

[ Index of Refraction ]:
1.585

MSDS

Click to get detail MSDS

Safety Information

[ Symbol ]:

GHS07

[ Signal Word ]:
Warning

[ Hazard Statements ]:
H302

[ Personal Protective Equipment ]:
dust mask type N95 (US);Eyeshields;Gloves

[ Hazard Codes ]:
Xn:Harmful

[ Risk Phrases ]:
R22

[ Safety Phrases ]:
S22-S2

[ RIDADR ]:
UN 3077 9/PG 3

[ WGK Germany ]:
1

[ RTECS ]:
UV6260335

[ HS Code ]:
2933599090

Synthetic Route

Click to get detail 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

The infrared, Raman, NMR and UV spectra, ab initio calculations and spectral assignments of 2-amino-4-chloro-6-methoxypyrimidine.

.PubMed ID

The 2-amino-4-chloro-6-methoxypyrimidine abbreviated as ACMP have been investigated by both the experimental and theoretical methods; through this work we provide the essential fact about the structur...

Directed supramolecular assembly of infinite 1-D M(II)-containing chains (M = Cu, Co, Ni) using structurally bifunctional ligands.

Inorg. Chem. 44(14) , 4983-91, (2005)

The directed assembly of six different M(II) complexes (M = Cu, Co, and Ni) into infinite chains has been achieved by combining anionic chelating ligands (for controlling the coordination geometry) wi...

Fast separation of pyrimidine derivatives by capillary electrochromatography on ion-exchange/reversed-phase mixed-mode stationary phases.

J. Chromatogr. A. 911(2) , 277-83, (2001)

This work describes the use of mixed-mode stationary phases which exhibit both strong ion-exchange (either cation-exchange, SCX, or anion-exchange, SAX) and reversed-phase chromatographic characterist...