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Detail of "7244-78-2"

  • MSDS Download
  • CAS Number:
  • 7244-78-2
  • Name:
  • Benzene,1-butoxy-4-nitro-

  • Molecular Structure:
  • Formula:
  • C10H13NO3
  • Molecular Weight:
  • 195.22
  • Synonyms:
  • Ether,butyl p-nitrophenyl (7CI,8CI);1-Butoxy-4-nitrobenzene;4-Butoxynitrobenzene;Ba 2692;Butyl 4-nitrophenyl ether;Butyl p-nitrophenyl ether;NSC 86583;p-(Butoxy)nitrobenzene;p-Nitrobutoxybenzene;p-Nitrophenyl butyl ether;
  • Density:
  • 1.116 g/cm3
  • Boiling Point:
  • 308 °C at 760 mmHg
  • Flash Point:
  • 135.5 °C
  • Hazard Symbols:
  • IrritantXi

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CAS No.7244-78-2 Benzene,1-butoxy-4-nitro-

Supplier:Pfaltz & Bauer, Inc. [ United States]

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Reference

Metabolism of butyl p-nitrophenyl ether in vitro with rabbit liver preparations
Metabolism of butyl p-nitrophenyl ether in vitro with rabbit liver preparations. Tsuji, Hiroshi; Yoshimura, Hidetoshi; Tsukamoto, Hisao (Fac. Pharm. Sci., Kyushu Univ., Fukuoka, Japan). Xenobiotica, 8(4), 245-51 (English) 1978. CODEN: XENOBH. ISSN: 0049-8254. DOCUMENT TYPE: Journal CA Section: 3 (Biochemical Interactions) Metab. of Bu p-nitrophenyl ether [7244-78-2] by rabbit liver prepns. involved an initial microsomal hydroxylation at a, w-1, or the w positions of the Bu chain. w-Hydroxybutyl p-nitrophenyl ether (I) [60222-69-7] was oxidized by the sol. fraction to the corresponding (w-1)-oxo deriv. which spontaneously decompd. to give p-nitrophenol [100-02-7]. I was further oxidized by the sol. fraction to p-nitrophenoxybutyric acid [28341-54-0].
Azo compound
Azo compound. Murakami, Yasuo; Tanaka, Hideo; Torii, Shigeru (Nippon Kayaku Co., Ltd.In this study,7244-78-2 is also used., Japan). Jpn. Kokai Tokkyo Koho JP 61246392 A2 1 Nov 1986 Showa, 5 pp. (Japan) CODEN: JKXXAF. CLASS: ICM: C25B003-04. APPLICATION: JP 85-87454 25 Apr 1985. DOCUMENT TYPE: Patent CA Section: 72 (Electrochemistry) A method for prepg. an azo compd. (I) (R, R1 = H, halo, C1-4 alkyl, C1-4 alkoxy, Ph, OH, acyl, amino, or carboxyl) involves electrochem. redn. of II in an alk. alc. solvent. Thus, 2,2'-dimethoxyazobenzene was prepd. by reducing o-nitroanisole in MeOH-KOH soln. .
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