| Weight | 42.041 g/mol |
|---|---|
| Formula | CH2N2 |
| Hydrogen Acceptors | 0 |
| Hydrogen Donors | 0 |
| Aromatic Rings | 0 |
| Rotatable Bonds | 0 |
DIAZOMETHANE (334-88-3)
Diazirine
Score:
#372 in Biochemistry
,
#529 in Physics
,
#1537 in Chemistry
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- Esterification of Fatty Acids with Diazomethane on a Small Scale (Analytical Chemistry, 1960)
- Photolabeling of Prostaglandin Endoperoxide H Synthase-1 with 3-Trifluoro-3-(m-Iiodophenyl)diazirine as a Probe of Membrane Association and the Cyclooxygenase Active Site (Journal of Biological Chemistry, 1996)
- Reactions of diazomethane on transition-metal surfaces and their relationship to the mechanism of the Fischer-Tropsch reaction (Journal of the American Chemical Society, 1980)
- Simple device for preparing ethereal diazomethane without resorting to codistillation (Analytical Chemistry, 1973)
- A new method for the preparation of diazomethane (Recueil des Travaux Chimiques des Pays-Bas, 2010)
- Cyclopropanation with Diazomethane and Bis(oxazoline)palladium(II) Complexes (Journal of Organic Chemistry, 1997)
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Predict GHS Hazards for Any Chemical in silico.
Including Acute Oral Tox, Skin Sensitization, Eye Irritation, Aquatic Tox, & more. - H220: Extremely flammable gas
Danger Flammable gases - Category 1 - H317: May cause an allergic skin reaction
Warning Sensitization, Skin - Category 1 - H334: May cause allergy or asthma symptoms or breathing difficulties if inhaled
Danger Sensitization, respiratory - Category 1 - H350: May cause cancer
Danger Carcinogenicity - Category 1A, 1B - Diazirine
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SMILESC=[N+]=[N-]
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- Pubchem - DIAZOMETHANE
- Wikipedia - diazomethane
Diazomethane is the chemical compound CH2N2, discovered by German chemist Hans von Pechmann in 1894. It is the simplest diazo compound. In the pure form at room temperature, it is an extremely sensitive explosive yellow gas; thus, it is almost universally used as a solution in diethyl ether.
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