Weight | 105.524 g/mol |
---|---|
Formula | C3H4ClNO |
Hydrogen Acceptors | 2 |
Hydrogen Donors | 0 |
Aromatic Rings | 0 |
Rotatable Bonds | 2 |
2-Chloroethyl isocyanate (1943-83-5)
NSC-87418 · NSC 87418
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LabBot
- Inhibition of DNA repair by the 1,3-bis(2-chloroethyl)-1-nitrosourea breakdown product, 2-chloroethyl isocyanate. (Cancer Research, 1974)
- Inhibition of the Ligase Step of Excision Repair by 2-Chloroethyl Isocyanate, a Decomposition Product of 1,3-Bis(2-chloroethyl)-1-nitrosourea (Cancer Research, 1978)
- Glutathione and N-acetylcysteine conjugates of 2-chloroethyl isocyanate. Identification as metabolites of N,N'-bis(2-chloroethyl)-N-nitrosourea in the rat and inhibitory properties toward glutathione reductase in vitro (Chemical Research in Toxicology, 1993)
- Active site specific inactivation of chymotrypsin by cyclohexyl isocyanate formed during degradation of the carcinostatic 1-(2-chloroethyl)-3-cyclohexyl-1-nitrosourea. (Biochemistry, 1977)
- Effect of carbamate thioester derivatives of methyl- and 2-chloroethyl isocyanate on glutathione levels and glutathione reductase activity in isolated rat hepatocytes (Biochemical Pharmacology, 1994)
- Marquage par 14C du Chloro-2 Ethyl Isocyanate. Application au Marquage de Chloroethyl Tetrazinone et de Chloroethylnitrosourees (Journal of Labelled Compounds and Radiopharmaceuticals, 1988)
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Including Acute Oral Tox, Skin Sensitization, Eye Irritation, Aquatic Tox, & more. - NSC-87418
- NSC 87418
-
SMILESC(CCl)N=C=O
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InChIKeyBCMYXYHEMGPZJN-UHFFFAOYSA-N
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Similar Compounds
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