530301
2-(Chloromethyl)-3,4-dimethoxypyridine hydrochloride
97%
Synonym(s):
2-(Chloromethyl)-3,4-dimethoxypyridinium hydrochloride
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About This Item
Empirical Formula (Hill Notation):
C8H11Cl2NO2
CAS Number:
Molecular Weight:
224.08
Beilstein:
5360726
EC Number:
MDL number:
UNSPSC Code:
12352100
PubChem Substance ID:
NACRES:
NA.22
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Quality Level
Assay
97%
mp
155 °C (dec.) (lit.)
SMILES string
Cl[H].COc1ccnc(CCl)c1OC
InChI
1S/C8H10ClNO2.ClH/c1-11-7-3-4-10-6(5-9)8(7)12-2;/h3-4H,5H2,1-2H3;1H
InChI key
YYRIKJFWBIEEDH-UHFFFAOYSA-N
General description
2-(Chloromethyl)-3,4-dimethoxypyridine hydrochloride (CDP) can be synthesized using maltol as a starting material. CDP and DMS (dimethyl sulfate) are used in the preparation of pantoprazole sodium (PPS), an antiulcerative drug. The quantification of CDP and DMS in PPS can be done simultaneously by gas chromatography–mass spectrometry (GC-MS) method.
Application
2-(Chloromethyl)-3,4-dimethoxypyridine hydrochloride may be used as a precursor for the preparation [(2-pyridyl)-2-ethyl]-[3,4-dimethoxy-(2-pyridylmethyl)]-N-methylamine.
Signal Word
Danger
Hazard Statements
Precautionary Statements
Hazard Classifications
Acute Tox. 4 Dermal - Acute Tox. 4 Oral - Aquatic Chronic 2 - Eye Dam. 1 - Skin Irrit. 2 - Skin Sens. 1 - STOT RE 2
Storage Class Code
11 - Combustible Solids
WGK
WGK 3
Flash Point(F)
Not applicable
Flash Point(C)
Not applicable
Personal Protective Equipment
dust mask type N95 (US), Eyeshields, Gloves
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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)
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)
The Synthesis of 2-chloromethyl-3,4-dimethoxypyridine Hydrochloride.
L DL, et al.
Journal of Jiangxi Normal University (Natural Science Edition), 42-45 (2003)
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