Ethoxymethaniminium chloride

Names

[ Name ]:
Ethoxymethaniminium chloride

[Synonym ]:
Ethoxymethaniminium chloride
HCl*HN=CHOEt
formimidic acid ethyl ester hydrochloride
Methaniminium, 1-ethoxy-, chloride (1:1)
ethyl formimidate.HCl
O-ethyl formimidate hydrochloride
Ethyl formalimidate HCl
MFCD00192154
Ethyl formimidate hydrochloride
ethyl methanimidate hydrochloride

Chemical & Physical Properties

[ Density]:
0.88g/cm3

[ Boiling Point ]:
31.7ºC at 760mmHg

[ Melting Point ]:
75ºC

[ Molecular Formula ]:
C₃H₈ClNO

[ Molecular Weight ]:
109.555

[ Exact Mass ]:
109.029442

[ PSA ]:
33.08000

[ LogP ]:
1.53170

[ Vapour Pressure ]:
597mmHg at 25°C

[ Index of Refraction ]:
1.388

[ Storage condition ]:
2-8°C

MSDS

Click to get detail 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-S37/39

[ RIDADR ]:
NONH for all modes of transport

[ WGK Germany ]:
3

[ HS Code ]:
2925290090

Synthetic Route

Click to get detail synthetic route

Precursor & DownStream

Precursor

DownStream

Customs

[ HS Code ]: 2925290090

[ Summary ]:
2925290090 other imines and their derivatives; salts thereof。Supervision conditions:None。VAT:17.0%。Tax rebate rate:9.0%。MFN tariff:6.5%。General tariff:30.0%

Articles

Purines, pyrimidines, and imidazoles. XL. A new synthesis of a D-ribofuranosylamine derivative and its use in the synthesis of pyrimidine and imidazole nucleosides.

J. Chem. Soc. Perkin Trans. I 16 , 1720-31, (1973)

Synthesis of the S-Triazine System. Iii. 1 Trimerization of Imidates. Schaefer FC and Peters GA.

J. Org. Chem. 26(8) , 2771-84, (1961)

Purines, pyrimidines, and imidazoles. Part XLI. Glycofuranosylamines derived from D-xylose, D-glucose, D-mannose, and L-rhamnose and their use in the synthesis of pyrimidine and imidazole nucleosides. Cusack NJ, et al.

J. Chem. Soc. Perkin Trans. I , 73-81, (1974)