Detail of "53416-46-9"
- CAS Number:
- 53416-46-9
- Name:
Oxazole,4,5-dihydro-2-(4-methoxyphenyl)-4,4-dimethyl-
- Molecular Structure:
- Formula:
- C12H15 N O2
- Molecular Weight:
- 205.25
- Synonyms:
- 2-(4-Methoxyphenyl)-4,4-dimethyl-2-oxazoline;4,4-Dimethyl-2-p-methoxyphenyl-2-oxazoline; 4,5-Dihydro-2-(4-methoxyphenyl)-4,4-dimethyloxazole;NSC 620123
Oxazole,4,5-dihydro-2-(4-methoxyphenyl)-4,4-dimethyl-
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Reference
- A new 7,12-dimethylbenz[a]anthracene synthesis: 9-methoxy- and 10-methoxy-7,12-dimethylbenz[a]anthracene
- A new 7,12-dimethylbenz[a]anthracene synthesis: 9-methoxy- and 10-methoxy-7,12-dimethylbenz[a]anthracene. Newman, Melvin S.In this article, certain chemicals are used. One of their cas registry numbers is 53416-46-9 ; Kumar, Subodh (Dep. Chem., Ohio State Univ., Columbus, Ohio, USA). J. Org. Chem., 43(2), 370-1 (English) 1978. CODEN: JOCEAH. DOCUMENT TYPE: Journal CA Section: 26 (Condensed Aromatic Compounds) Hydrolysis of the reaction product of 2-(2-lithio-4-methoxyphenyl)-4,4-dimethyl-2-oxazoline with Me 2-naphthyl ketone affords 5-methoxy-3-methyl-3-(2-naphthyl)phthalide which is converted by three known steps to 9-methoxy-7,12-dimethylbenz[a]anthracene (I). Similarly, Me 1-naphthyl ketone affords 10-methoxy-7,12-dimethylbenz[a]anthracene. Overall yields were 27-33%.In this study，53416-46-9 is also used. ..
- A new 7,12-dimethylbenz[a]anthracene synthesis: 9-methoxy- and 10-methoxy-7,12-dimethylbenz[a]anthracene
- A new 7,12-dimethylbenz[a]anthracene synthesis: 9-methoxy- and 10-methoxy-7,12-dimethylbenz[a]anthracene. Newman, Melvin S.In this article, certain chemicals are used. One of their cas registry numbers is 53416-46-9 ; Kumar, Subodh (Dep. Chem., Ohio State Univ., Columbus, Ohio, USA). J. Org. Chem., 43(2), 370-1 (English) 1978. CODEN: JOCEAH. DOCUMENT TYPE: Journal CA Section: 26 (Condensed Aromatic Compounds) Hydrolysis of the reaction product of 2-(2-lithio-4-methoxyphenyl)-4,4-dimethyl-2-oxazoline with Me 2-naphthyl ketone affords 5-methoxy-3-methyl-3-(2-naphthyl)phthalide which is converted by three known steps to 9-methoxy-7,12-dimethylbenz[a]anthracene (I). Similarly, Me 1-naphthyl ketone affords 10-methoxy-7,12-dimethylbenz[a]anthracene. Overall yields were 27-33%.In this study，53416-46-9 is also used. ..