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2-Methyl-1,3-dioxole | 68882-31-5

中文名称
——
中文别名
——
英文名称
2-Methyl-1,3-dioxole
英文别名
2-Methyl-1,3-dioxolan;2-Methyl-2H-1,3-dioxole
2-Methyl-1,3-dioxole化学式
CAS
68882-31-5
化学式
C4H6O2
mdl
——
分子量
86.0904
InChiKey
WGHMWTYSXYBZSU-UHFFFAOYSA-N
BEILSTEIN
——
EINECS
——
  • 物化性质
  • 计算性质
  • ADMET
  • 安全信息
  • SDS
  • 制备方法与用途
  • 上下游信息
  • 反应信息
  • 文献信息
  • 表征谱图
  • 同类化合物
  • 相关功能分类
  • 相关结构分类

计算性质

  • 辛醇/水分配系数(LogP):
    0.8
  • 重原子数:
    6
  • 可旋转键数:
    0
  • 环数:
    1.0
  • sp3杂化的碳原子比例:
    0.5
  • 拓扑面积:
    18.5
  • 氢给体数:
    0
  • 氢受体数:
    2

SDS

SDS:fa9512329f13c625d13a6068bf1ad17e
查看

反应信息

  • 作为反应物:
    描述:
    2-Methyl-1,3-dioxole 生成 (1R,2R,3S,7R,8S,9S)-5-methyl-4,6-dioxatetracyclo[7.2.2.02,8.03,7]tridec-12-ene-10,10,11,11-tetracarbonitrile
    参考文献:
    名称:
    MATTAY J.; LEISMANN H.; SCHARF H.-D., CHEM. BER., 1979, 112, NO 2, 577-599
    摘要:
    DOI:
  • 作为产物:
    描述:
    17-methyl-16,18-dioxapentacyclo[6.6.5.02,7.09,14.015,19]nonadeca-2,4,6,9,11,13-hexaene 、 potassium carbonate对叔丁基邻苯二酚 以75%的产率得到
    参考文献:
    名称:
    OSSELTON, E. M.;CORNELISSE, J.;MATTAY, J., J. PHOTOCHEM., 1985, 31, N 2-3, 381-386
    摘要:
    DOI:
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文献信息

  • Atta, Ferial M.; Betz, Rainer; Schmid, Bruno, Chemische Berichte, 1986, vol. 119, # 2, p. 472 - 481
    作者:Atta, Ferial M.、Betz, Rainer、Schmid, Bruno、Schmidt, Richard R.
    DOI:——
    日期:——
  • ATTA, F. M.;BETZ, R.;SCHMID, B.;SCHMIDT, R. R., CHEM. BER., 1986, 119, N 2, 472-481
    作者:ATTA, F. M.、BETZ, R.、SCHMID, B.、SCHMIDT, R. R.
    DOI:——
    日期:——
  • OSSELTON, E. M.;CORNELISSE, J.;MATTAY, J., J. PHOTOCHEM., 1985, 31, N 2-3, 381-386
    作者:OSSELTON, E. M.、CORNELISSE, J.、MATTAY, J.
    DOI:——
    日期:——
  • MATTAY J.; LEISMANN H.; SCHARF H.-D., CHEM. BER., 1979, 112, NO 2, 577-599
    作者:MATTAY J.、 LEISMANN H.、 SCHARF H.-D.
    DOI:——
    日期:——
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同类化合物

1,4:6,9-二亚甲基吡啶联氮基[1,2-a]哒嗪(9CI) 1,3-苯并二氧戊环-4,7-二酮 1,3-二噁唑,4-甲基- 4,7-Dihydrobenzo[1,3]dioxole 1,3-Dioxole, 2,2-difluoro- 2,4-dimethyl-[1,3]dioxole 2-Methyl-1,3-dioxole 2,2,4-trifluoro-1,3-dioxole [1,3]Dioxolo[4,5-f][1,4]diazocine 2H-Thieno[3',4':3,4]cyclobuta[1,2-d][1,3]dioxole 2-tert-Butyl-4-methyl-2H-1,3-dioxole 2-(2H-1,3-Dioxol-2-ylidene)-2H-1,3-dioxole 1-(methoxycarbonyl)-2-methyl-4-isopropyl-3,5-dioxacyclopent-1-ene 5,6-Dimethyl-2H-1,3-benzodioxole-4,7-dione 4-Methyl-2-(1-methyl-butyl)-[1,3]dioxole 2-Hexyl-4-methyl-[1,3]dioxole 4-Methyl-2-pentyl-[1,3]dioxole 2-ethyl-4-methyl-1,3-dioxole ethyl 6H-cyclohepta[d][1,3]dioxole-6-carboxylate 2-acetyl-3-methyl-5-(2-furoyl)-3,5-dioxacyclopent-1-ene 4,5-dimethyl-1,3-dioxole (5aS)-5aH-[1,3]dioxolo[4,5-e]indazole (5aR)-5aH-[1,3]dioxolo[4,5-e]indazole 2-[(5R)-5-amino-4H-1,3-benzodioxol-5-yl]ethanol 2-[(5S)-5-amino-4H-1,3-benzodioxol-5-yl]ethanol methyl (2S)-2-methyl-1,3-dioxole-4-carboxylate N-[(2S)-2-(methoxymethyl)pyrrolidin-1-yl]-1,3-dioxole-4-carboxamide 3-(1,3-Dioxol-4-yl)prop-2-yn-1-ol Fluoroethane;fluoromethyl hypofluorite;2,2,4-trifluoro-5-(fluoromethoxy)-1,3-dioxole N-(oxolan-2-ylmethyl)-1,3-dioxole-4-carboxamide [(2,4-Difluoro-1,3-dioxol-2-yl)-difluoromethyl] hypofluorite;ethoxyethane [6-(1,3-Dioxol-4-ylmethylidene)cyclohexa-1,3-dien-1-yl]boronic acid 3,4-Dihydro-1,2-benzodioxol-7-one;hydrobromide methyl (2R)-2-methyl-1,3-dioxole-4-carboxylate 2,2-Difluoro-1,3-dioxole;ethane Difluoromethane;fluoroethane;fluoromethane;fluoromethyl hypofluorite;2,2,4-trifluoro-5-(fluoromethoxy)-1,3-dioxole 4-(2,3-Dihydrothiophen-2-yl)-1,3-dioxole 3-propyl-5,6,7,7a-tetrahydro-4H-1,2-benzodioxole-5-carboxylic acid 4-(3-Methoxybuta-1,3-dien-2-yl)-5-[1-(3-methoxy-2,4-dimethylpent-3-enoxy)ethenyl]-1,3-dioxole 4-Butyl-5-ethyl-1,3-dioxole 4-Ethyl-1,3-dioxole N-(1,3-dioxol-4-yl)acetamide Ethane;2-methylidene-1,3-dioxole 5-(2-Methylpropyl)-4,5-dihydro-1,3-benzodioxole 3-(1,3-Dioxol-2-yl)prop-2-enal (1-Carbamoylcyclobutyl) 1,3-dioxole-4-carboxylate 4-(Cyclohexa-1,3-dien-1-ylmethyl)-1,3-dioxole [Difluoro-(2,4,5-trifluoro-1,3-dioxol-2-yl)methyl] hypofluorite;2-ethoxy-1,1,1-trifluoroethane 2-Hepta-1,3-dienyl-1,3-dioxole 4-Methylsulfanyl-5-propan-2-yl-1,3-dioxole