nitroanisidinen.

Brit.

/ˌnʌɪtrəʊəˈnɪsᵻdiːn/, U.S.

/ˈˌnaɪtroʊəˈnɪsᵻdin/

Forms: 1800s nitranisidine, 1900s– nitroanisidine.

Origin: Formed within English, by compounding; modelled on a German lexical item. Etymons: nitro- comb. form, anisidine n. at anis- comb. form .

Etymology: < nitro- comb. form + anisidine n. at anis- comb. form , after German Nitranisidin (A. Cahours 1850, in Ann. der Chem. u. Pharm. 74 301), itself after French anisidine nitrique (A. Cahours 1849, in Ann. de chim. et de physique 27 439).

Chemistry.

Any of various yellow or orange crystalline compounds, C₆H₃(OCH₃₎(NO₂)(NH₂), which are amino derivatives of nitroanisole.

ΘΚΠ

the world > matter > chemistry > crystallography (general) > crystal (general) > [noun] > crystalline compound > specific

alcoholate1816

alcoate1828

absinthin1834

nitroaniline1848

nitroanisidine1850

purpurein1864

quinizarin1873

phenazoxine1887

phenanthridine1890

1850 Philos. Trans. (Royal Soc.) 140 111 (table) Anisidine..Nitranisidine..Dinitranisidine.

1852 W. Gregory Handbk. Org. Chem. (ed. 3) 152 Nitranisole..when acted on by sulphuret of ammonium, yields the base anisidine, C₁₄H₉NO₂; and dinitranisole yields the base nitranisidine.

1879 H. Watts Dict. Chem. I. 304 Nitranisidine dissolves readily in acids, and with many of them forms crystalline salts.

1953 A. G. E. Pearse Histochem. iv. 64 I have attempted to get rid of tyrosine and histidine by initial coupling with a diazonium compound, using, for convenience, a stable diazotate of 5-nitroanisidine.

1998 Biochimica et Biophysica Acta 1379 391 All three substituents (amino, methoxyl and nitro groups) are necessary components of nitroanisidines for induction of CYP1A enzymes.

This entry has been updated (OED Third Edition, December 2003; most recently modified version published online March 2022).

单词	nitroanisidine
释义	nitroanisidinen. Brit. /ˌnʌɪtrəʊəˈnɪsᵻdiːn/, U.S. /ˈˌnaɪtroʊəˈnɪsᵻdin/ Forms: 1800s nitranisidine, 1900s– nitroanisidine. Origin: Formed within English, by compounding; modelled on a German lexical item. Etymons: nitro- comb. form, anisidine n. at anis- comb. form . Etymology: < nitro- comb. form + anisidine n. at anis- comb. form , after German Nitranisidin (A. Cahours 1850, in Ann. der Chem. u. Pharm. 74 301), itself after French anisidine nitrique (A. Cahours 1849, in Ann. de chim. et de physique 27 439). Chemistry. Any of various yellow or orange crystalline compounds, C₆H₃(OCH₃₎(NO₂)(NH₂), which are amino derivatives of nitroanisole. ΘΚΠ the world > matter > chemistry > crystallography (general) > crystal (general) > [noun] > crystalline compound > specific alcoholate1816 alcoate1828 absinthin1834 nitroaniline1848 nitroanisidine1850 purpurein1864 quinizarin1873 phenazoxine1887 phenanthridine1890 1850 Philos. Trans. (Royal Soc.) 140 111 (table) Anisidine..Nitranisidine..Dinitranisidine. 1852 W. Gregory Handbk. Org. Chem. (ed. 3) 152 Nitranisole..when acted on by sulphuret of ammonium, yields the base anisidine, C₁₄H₉NO₂; and dinitranisole yields the base nitranisidine. 1879 H. Watts Dict. Chem. I. 304 Nitranisidine dissolves readily in acids, and with many of them forms crystalline salts. 1953 A. G. E. Pearse Histochem. iv. 64 I have attempted to get rid of tyrosine and histidine by initial coupling with a diazonium compound, using, for convenience, a stable diazotate of 5-nitroanisidine. 1998 Biochimica et Biophysica Acta 1379 391 All three substituents (amino, methoxyl and nitro groups) are necessary components of nitroanisidines for induction of CYP1A enzymes. This entry has been updated (OED Third Edition, December 2003; most recently modified version published online March 2022). < n.1850
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