Acetimidamide hydrochloride

Suppliers

Names

[ CAS No. ]:
124-42-5

[ Name ]:
Acetimidamide hydrochloride

[Synonym ]:
Acetimidamide hydrochloride
Acetamidine, monohydrochloride
Ethanimidamide, hydrochloride (1:1)
ethanimidamidhydrochlorid
MFCD00013016
Ethanimidamide hydrochloride (1:1)
α-Amino-α-iminoethane hydrochloride
EINECS 204-700-9
Acetamidine Hydrochloride

Chemical & Physical Properties

[ Boiling Point ]:
62.8ºC at 760mmHg

[ Melting Point ]:
165-170 °C(lit.)

[ Molecular Formula ]:
C2H7ClN2

[ Molecular Weight ]:
94.543

[ Flash Point ]:
26.1ºC

[ Exact Mass ]:
94.029778

[ PSA ]:
49.87000

[ LogP ]:
1.54430

[ Vapour Pressure ]:
176mmHg at 25°C

[ Index of Refraction ]:
1.458

[ Water Solubility ]:
1 g/mL

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 ]:
R36/38

[ Safety Phrases ]:
S26-S37/39

[ RIDADR ]:
NONH for all modes of transport

[ WGK Germany ]:
3

[ HS Code ]:
29252000

Synthetic Route

Precursor & DownStream

Precursor

  • N-hydroxyethanimidamide hydrochloride
  • Acetonitrile
  • Acetamide
  • Ethanol
  • acetamide oxime
  • Ethyl acetimidate hydrochloride
  • Ammonia

DownStream

  • 6-Bromo-2-methylquinazolin-4(3H)-one
  • (2-Methyl-1H-imidazol-4-yl)methanol
  • 1,1,3,3,3-Pentafluoro-2-trifluoromethylpropyl methyl ether
  • 4-fluoro-6-methoxy-2-methyl-5-(trifluoromethyl)pyrimidine
  • 4,6-Dihydroxy-2-methylpyrimidine
  • 5-Pyrimidineaceticacid, 3,4-dihydro-2-methyl-4-oxo-, ethyl ester
  • N'-phenylethanimidamide
  • 2-Methylpyrimidine
  • 2-Methylpyrimidine-5-carbaldehyde
  • 2,6-Dimethyl-4-pyrimidinamine

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

Selectivity of externally facing ion-binding sites in the Na/K pump to alkali metals and organic cations.

Proc. Natl. Acad. Sci. U. S. A. 107(43) , 18718-23, (2010)

The Na/K pump is a P-type ATPase that exchanges three intracellular Na(+) ions for two extracellular K(+) ions through the plasmalemma of nearly all animal cells. The mechanisms involved in cation sel...

Highly efficient copper-catalyzed cascade synthesis of quinazoline and quinazolinone derivatives.

Chem. Commun. (Camb.) (47) , 6333-5, (2008)

We have developed a general and highly efficient copper-catalyzed method for synthesis of quinazoline and quinazolinone derivatives, the target products were obtained in good to excellent yields via c...

A synthesis of acetamidines.

J. Org. Chem. 76(6) , 1683-91, (2011)

The condensation of primary amine with N,N-dimethylacetamide dimethyl acetal yields a mixture of acetamidine and imidate ester. The product distribution in this reaction depends on the temperature, so...


More Articles


Related Compounds

  • 2-chloroacetimidamide hydrochloride
  • 2-(Methylthio)acetimidamide hydrochloride
  • 2-(3-FLUOROPHENYL)ACETIMIDAMIDE HYDROCHLORIDE
  • 2-(3,4-difluorophenyl)acetimidamide hydrochloride
  • 2-(4-(TERT-BUTYL)PHENOXY)ACETIMIDAMIDE HYDROCHLORIDE
  • 2-(4-(Trifluoromethyl)phenyl)acetimidamide hydrochloride
  • 1-[3-(Trifluoromethoxy)phenyl]cyclopropane-1-carboxylic acid
  • 1-[2-(Trifluoromethoxy)phenyl]cyclopropane-1-carbonitrile
  • 1-[3-(Trifluoromethoxy)phenyl]cyclopropane-1-carbonitrile
  • 1-[4-(Trifluoromethyl)pyridin-3-yl]cyclopropan-1-amine
  • 1-(2-(Trifluoromethyl)pyridin-3-yl)cyclopropan-1-amine
  • 1-(3-(Trifluoromethyl)pyridin-4-yl)cyclopropan-1-amine
  • Cyclopropanecarbothioamide, 1-(3-pyridinyl)-
  • 1-(4-Fluorophenyl)cyclopropane-1-carbothioamide
  • 1-(4-Bromophenyl)cyclopropane-1-carbothioamide
  • 1-[3-(Trifluoromethoxy)phenyl]cyclobutane-1-carboxylic acid
The content on this webpage is sourced from various professional data sources. If you have any questions or concerns regarding the content, please feel free to contact service1@chemsrc.com.