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Detail of "5076-19-7"

  • MSDS Download
  • CAS Number:
  • 5076-19-7
  • Name:
  • Oxirane,2,2,3-trimethyl-

  • Molecular Structure:
  • Formula:
  • C5H10 O
  • Molecular Weight:
  • 86.15
  • Synonyms:
  • Butane,2,3-epoxy-2-methyl- (6CI,7CI,8CI); Oxirane, trimethyl- (9CI); (?à)-2,2,3-Trimethyloxirane;2,2,3-Trimethyloxirane; 2,3-Epoxy-2-methylbutane; 2-Isopentene oxide;2-Methyl-2,3-epoxybutane; 2-Methyl-2-butene oxide; Trimethylethylene oxide;Trimethyloxacyclopropane; Trimethyloxirane; b-Isoamylene oxide
  • Density:
  • 0.838g/cm3
  • Boiling Point:
  • 60.5°Cat760mmHg
  • Flash Point:
  • °C
  • Hazard Symbols:
  • FXi
  • Risk Codes:
  • R11;R36/37/38;
  • Safety:
  • Moderately toxic by ingestion and intraperitoneal routes. When heated to decomposition it emits acrid smoke and irritating fumes. Details

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Reference

Oxirane compounds by autoxidation
Oxirane compounds by autoxidation. Barone, Bruno J. (Petro-Tex Chemical Corp., USA). U.S. US 3987069 19 Oct 1976, 4 pp. (English). (United States of America). CODEN: USXXAM. CLASS: IC: C07D301-22. NCL: 260348500V. APPLICATION: US 71-170283 9 Aug 1971.Several substances with their cas registry numbers 5076-19-7 and 513-35-9 may be metioned in this study. DOCUMENT TYPE: Patent CA Section: 27 (Heterocyclic Compounds (One Hetero Atom)) B phosphate and Li phosphate were used as catalysts for oxidn. of Me2C:CHMe (I) with air to 2,3-epoxy-2-methylbutane (II). In a typical run, using B phosphate as a catalyst at 90.degree. and 400 psi air for 3.33 hr, conversion of I was 13.8 mole% and selectivity for II was 65.8%. .
2-Methyl-2,3-epoxybutane
2-Methyl-2,3-epoxybutane. Yurzhenko, S. A. (Lvov Polytechnic Institute, USSR). U.S.S.R. SU 533595 30 Oct 1976 From: Otkrytiya, Izobret., Prom. Obraztsy, Tovarnye Znaki 1976, 53(40), 63. (Russian).There are some reagents with their cas registry numbers 5076-19-7 and 7440-48-4 are used in this study. (Union of Soviet Socialist Republics). CODEN: URXXAF. CLASS: IC: C07D303-04. APPLICATION: SU 74-2041516 5 Jun 1974. DOCUMENT TYPE: Patent CA Section: 27 (Heterocyclic Compounds (One Hetero Atom)) The title compd. was prepd. by oxidn. of 2-methyl-2-butene (I) with O or an O-contg. gas at 120-35.degree. in the presence of a Mo-contg. catalyst, e.g., Co naphthenate and Mo resinate. The selectivity of the process and yield of product were improved by using a I-isopentane mixt. at 40-50 atm. and a 30 l./h gas feed rate. .
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