Ethoxymethaniminium chloride

Suppliers

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

Ethanol
(Z)-Methanimidic acid
HYDROGEN CYANIDE
Hydrochloric acid
Diethyl ether

DownStream

N-Methylformanilide
N-formylacetamide
Benzene,1-(diethoxymethyl)-3-nitro-
Benzene,1-(diethoxymethyl)-4-methoxy-
3-Ethoxyandrosta-3,5-dien-17-one
4H-1,2,4-Triazol-4-amine
FORMAMIDOXIME
Cinnamaldehyde, diethyl acetal
Basic Red 12

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)

Strontium chloride-Sr82
Benzenebutanoyl chloride, 3-chloro-
cyclopentadienylmagnesium chloride
Benzoyl chloride, 4-(1-methylpropyl)- (9CI)
methylsulfanylformyl chloride
dodecanoyl chloride,hydrofluoride
2-(1H-indol-1-yl)-1-((1R,5S)-3-(phenylsulfonyl)-8-azabicyclo[3.2.1]octan-8-yl)ethanone
2-(cyclopentylthio)-1-((1R,5S)-3-(phenylsulfonyl)-8-azabicyclo[3.2.1]octan-8-yl)ethanone
(5-methylpyrazin-2-yl)((1R,5S)-3-(phenylsulfonyl)-8-azabicyclo[3.2.1]octan-8-yl)methanone
(1-(3-(Cyclopropylamino)quinoxalin-2-yl)pyrrolidin-2-yl)methanol
tert-Butyl 2-((2,5-dichlorobenzyl)(methyl)carbamoyl)piperidine-1-carboxylate
4-(Prop-2-yn-1-yl)oxane-4-carboxylic acid
tert-Butyl 4-((3-chlorobenzyl)(methyl)carbamoyl)piperidine-1-carboxylate
(1-((6-Chloropyridazin-3-yl)methyl)pyrrolidin-2-yl)methanol
2-(2-oxo-2-((1R,5S)-3-(phenylsulfonyl)-8-azabicyclo[3.2.1]octan-8-yl)ethyl)pyridazin-3(2H)-one
(4-methyl-2-(1H-pyrrol-1-yl)thiazol-5-yl)((1R,5S)-3-(phenylsulfonyl)-8-azabicyclo[3.2.1]octan-8-yl)methanone

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