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2-Chloromethyl-3,4-dimethoxypyridinium chloride

Names

[ CAS No. ]:
72830-09-2

[ Name ]:
2-Chloromethyl-3,4-dimethoxypyridinium chloride

[Synonym ]:
2-(Chloromethyl)-3,4-dimethoxypyridine hydrochloride (1:1)
2-Chloromethyl-3,4-dimethoxypyridinium chloride
EINECS 416-440-5
MFCD02181083
Pyridine, 2-(chloromethyl)-3,4-dimethoxy-, hydrochloride (1:1)
T6NJ B1G CO1 DO1 &&HCl
2-(Chloromethyl)-3,4-dimethoxypyridinium hydrochloride
2-CHLORO METHYL- 3-4 DIMETHOXY PYRIDINE HCL

Biological Activity

[Description]:

2-(Chloromethyl)-3,4-dimethoxypyridine hydrochloride 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

Chemical & Physical Properties

[ Boiling Point ]:
293.9ºC at 760 mmHg

[ Melting Point ]:
155 °C (dec.)(lit.)

[ Molecular Formula ]:
C8H11Cl2NO2

[ Molecular Weight ]:
224.08

[ Flash Point ]:
131.6ºC

[ Exact Mass ]:
223.016678

[ PSA ]:
32.60000

MSDS

Safety Information

[ Symbol ]:

GHS05, GHS07, GHS08, GHS09

[ Signal Word ]:
Danger

[ Hazard Statements ]:
H302 + H312-H315-H317-H318-H373-H411

[ Precautionary Statements ]:
P273-P280-P305 + P351 + P338

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

[ Hazard Codes ]:
Xi:Irritant

[ Risk Phrases ]:
R21/22;R38;R41;R43;R48/22;R51/53

[ Safety Phrases ]:
S26-S36/37/39-S61-S2

[ RIDADR ]:
UN 3077 9/PG 3

[ WGK Germany ]:
3

[ Hazard Class ]:
9.0

[ HS Code ]:
2933399090

Synthetic Route

Precursor & DownStream

Customs

[ HS Code ]: 2933399090

[ Summary ]:
2933399090. other compounds containing an unfused pyridine ring (whether or not hydrogenated) in the structure. VAT:17.0%. Tax rebate rate:13.0%. . MFN tariff:6.5%. General tariff:20.0%

Articles

The Synthesis of 2-chloromethyl-3,4-dimethoxypyridine Hydrochloride. L DL, et al.

J. Jiangxi Normal Univ. (Nat. Sci. Ed.) , 42-45, (2003)

Validated chromatographic methods for the determination of process related toxic impurities in pantoprazole sodium. Raman NVVSS, et al.

Chromatographia 68(5-6) , 481-484, (2008)

fac-Cobalt (III)-azido complexes derived from substituted pyridyl-based tridentate amines. Massoud SS, et al.

Transition Met. Chem. (London) 39(5) , 585-591, (2014)


More Articles


Related Compounds

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