N-Boc-hydroxylamine

CAS: 36016-38-3

Ref. TR-B656470

Produktinformation

• Name: N-Boc-hydroxylamine
• Synonyme: N-Hydroxycarbamic Acid 1,1-Dimethylethyl Ester, Hydroxycarbamic Acid 1,1-Dimethylethyl Ester, Hydroxycarbamic Acid tert-Butyl Ester, 1,1-Dimethylethyl N-Hydroxycarbamate, N-(tert-Butoxycarbonyl)hydroxylamine, N-(tert-Butyloxycarbonyl)hydroxylamine, N-Hydroxycarbamic Acid tert-Butyl Ester, N-t-Butyloxycarbonyl Hydroxylamine, NSC 131086, NSC 144620, tert-Butoxycarbonylhydroxylamine, tert-Butoxyhydroxamic Acid, tert-Butyl N-Hydroxycarbamate, tert-Butyl Hydroxycarbamate, 1,1-Dimethylethyl N-hydroxycarbamate, Benzotriazol-1-YL 9-Fluorenylmethyl Carbonate, Carbamic acid, N-hydroxy-, 1,1-dimethylethyl ester, Carbamic acid, hydroxy-, 1,1-dimethylethyl ester, Carbamic acid, hydroxy-, tert-butyl ester, Hydroxycarbamic acid 1,1-dimethylethyl ester, N-Boc-hydroxyamine, N-Hydroxycarbamic acid tert-butyl ester, N-t-Butyloxycarbonyl hydroxylamine, Tert-Butyl Hydroxycarbamate, t-Butyl N-hydroxycarbomate, tert-Butoxyhydroxamic acid, tert-Butyl N-hydroxycarbamate, N-Boc hydroxylamine

Beschreibung

Applications N-Boc-hydroxylamine is the protected form of Hydroxylamine (HCl: H943705). Hydroxylamine is used as an inhibitor between Z and P680 in photosystem II within plant chloroplasts. Hydroxylamine is also known to induce chromosomal damage in mammalian cells, inducing mutagenesis.
References Ghanotakis, D. & Babcock, G.: FEBS Lett., 153, 231 (1983); Somers, C. & Hsu, T.: P. Natl. Acad. Sci. USA, 48, 937 (1962)

• Marke: TRC

Chemische Eigenschaften

• Molekulargewicht: 133.15
• Formel: C₅H₁₁NO₃
• Farbe/Form: Neat
• InChl: InChI=1S/C5H11NO3/c1-5(2,3)9-4(7)6-8/h8H,1-3H3,(H,6,7)
• InChI Key: InChIKey=DRDVJQOGFWAVLH-UHFFFAOYSA-N
• SMILES: CC(C)(C)OC(=O)NO