FORMAMIDOXIME structure
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Common Name | FORMAMIDOXIME | ||
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CAS Number | 624-82-8 | Molecular Weight | 60.05530 | |
Density | 1.29g/cm3 | Boiling Point | 224ºC at 760 mmHg | |
Molecular Formula | CH4N2O | Melting Point | 112-115ºC(lit.) | |
MSDS | Chinese USA | Flash Point | 89.3ºC | |
Symbol |
GHS07, GHS08 |
Signal Word | Warning |
Name | formamidoxime |
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Synonym | More Synonyms |
Density | 1.29g/cm3 |
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Boiling Point | 224ºC at 760 mmHg |
Melting Point | 112-115ºC(lit.) |
Molecular Formula | CH4N2O |
Molecular Weight | 60.05530 |
Flash Point | 89.3ºC |
Exact Mass | 60.03240 |
PSA | 58.61000 |
LogP | 0.06290 |
Index of Refraction | 1.471 |
Storage condition | 2-8°C |
CHEMICAL IDENTIFICATION
HEALTH HAZARD DATAACUTE TOXICITY DATA
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Symbol |
GHS07, GHS08 |
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Signal Word | Warning |
Hazard Statements | H302 + H312 + H332-H351 |
Precautionary Statements | P280 |
Personal Protective Equipment | dust mask type N95 (US);Eyeshields;Gloves |
Hazard Codes | Xn |
Risk Phrases | 20/21/22-40 |
Safety Phrases | 22-36 |
RIDADR | NONH for all modes of transport |
WGK Germany | 3 |
RTECS | LQ4632000 |
HS Code | 2925290090 |
~% FORMAMIDOXIME CAS#:624-82-8 |
Literature: Justus Liebigs Annalen der Chemie, , vol. 280, p. 325 |
~% FORMAMIDOXIME CAS#:624-82-8 |
Literature: Liebigs Annalen der Chemie, , vol. 166, p. 295 - 320 |
~% FORMAMIDOXIME CAS#:624-82-8 |
Literature: Justus Liebigs Annalen der Chemie, , vol. 166, p. 295 |
~% FORMAMIDOXIME CAS#:624-82-8 |
Literature: Justus Liebigs Annalen der Chemie, , vol. 166, p. 295 |
~%
Detail
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Literature: Journal fuer Praktische Chemie (Leipzig), , vol. <2>105, p. 24 |
~%
Detail
|
Literature: Journal fuer Praktische Chemie (Leipzig), , vol. <2>105, p. 24 |
Precursor 8 | |
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DownStream 10 | |
HS Code | 2925290090 |
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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% |
Antitumor activity of amidoximes (hydroxyurea analogs) in murine tumor systems.
Cancer Res. 38(5) , 1291-5, (1978) A series of amidoximes was prepared and evaluated for possible antitumor activity against L1210 leukemia. Three of the most active compounds in the L1210 system, formamidoxime, acetamidoxime, and 2-am... |
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Nitric oxide synthesis by tracheal smooth muscle cells by a nitric oxide synthase-independent pathway.
Am. J. Physiol. 275(5 Pt 1) , L895-901, (1998) Nitric oxide (NO) is known to be synthesized from L-arginine in a reaction catalyzed by NO synthase. Liver cytochrome P-450 enzymes also catalyze the oxidative cleavage of C==N bonds of compounds cont... |
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Effects of phenobarbital, beta-naphthoflavone, dexamethasone, and formamidoxime on the turnover of inducible microsomal proteins in cultured hepatocytes.
J. Biol. Chem. 256(24) , 13079-84, (1981) Microsomal proteins from cultured chick embryo hepatocytes were separated by polyacrylamide gel electrophoresis and their rate constants of degradation (Kd) were estimated using double isotope techniq... |
EINECS 210-865-8 |
carboxamidoxime |
Aminoformaldehyde oxime |
formamideoxime |
N-hydroxycarboximidamide |
n-hydroxy-methanimidamid |
formamidoxim |
n-hydroxymethanimidamide |
isuretin |
MFCD00008125 |
isouretin |