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2-allyl-5-methylpyrazine | 55138-63-1

中文名称
——
中文别名
——
英文名称
2-allyl-5-methylpyrazine
英文别名
2-methyl-5-prop-2-enylpyrazine
2-allyl-5-methylpyrazine化学式
CAS
55138-63-1
化学式
C8H10N2
mdl
——
分子量
134.181
InChiKey
JCZDTOUEQCNMKI-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

物化性质

  • 沸点:
    191.7±35.0 °C(Predicted)
  • 密度:
    0.982±0.06 g/cm3(Predicted)
  • 保留指数:
    1074

计算性质

  • 辛醇/水分配系数(LogP):
    1.3
  • 重原子数:
    10
  • 可旋转键数:
    2
  • 环数:
    1.0
  • sp3杂化的碳原子比例:
    0.25
  • 拓扑面积:
    25.8
  • 氢给体数:
    0
  • 氢受体数:
    2

反应信息

  • 作为产物:
    参考文献:
    名称:
    The effect of pH on the formation of aroma compounds produced by heating a model system containing l-ascorbic acid with l-threonine/l-serine
    摘要:
    The identification of aroma compounds, formed from the reactions of L-ascorbic acid with L-threonine/L-serine at five different pH values (5.00, 6.00, 7.00, 8.00, or 9.55) and 143 +/- 2 degrees C for 2 h, was performed using a SPME-GC-MS technique, and further use of LRI. The results showed 35 aroma compounds. The reaction between L-ascorbic acid and L-threonine/L-serine led mainly to the formation of pyrazines. Many of these were alkylpyrazines, such as 2-methylpyrazine, 2,5-dimethylpyrazine, 2-ethylpyrazine, 2-ethyl-6-methylpyrazine, 2-ethyl-5-methylpyrazine, 3-ethyl-2,5-dimethylpyrazine, 2,3-diethyl-5-methylpyrazine, and 3,5-diethyl-2-methylpyrazine; other compounds identified were furans and aldehydes. More volatiles were generated in L-ascorbic acid with L-threonine systems than in L-ascorbic acid with L-serine systems studies showed that furans such as furfural, 2-furanmethanol, benzofuran, 2,5-furandicar-boxaldehyde and 2-furfurylfuran were formed mainly at acidic pH. In contrast, higher pH values could promote the production of pyrazines. (C) 2009 Elsevier Ltd. All rights reserved.
    DOI:
    10.1016/j.foodchem.2009.06.026
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文献信息

  • The effect of pH on the formation of aroma compounds produced by heating a model system containing l-ascorbic acid with l-threonine/l-serine
    作者:Ai-Nong Yu、Ai-Dong Zhang
    DOI:10.1016/j.foodchem.2009.06.026
    日期:2010.3
    The identification of aroma compounds, formed from the reactions of L-ascorbic acid with L-threonine/L-serine at five different pH values (5.00, 6.00, 7.00, 8.00, or 9.55) and 143 +/- 2 degrees C for 2 h, was performed using a SPME-GC-MS technique, and further use of LRI. The results showed 35 aroma compounds. The reaction between L-ascorbic acid and L-threonine/L-serine led mainly to the formation of pyrazines. Many of these were alkylpyrazines, such as 2-methylpyrazine, 2,5-dimethylpyrazine, 2-ethylpyrazine, 2-ethyl-6-methylpyrazine, 2-ethyl-5-methylpyrazine, 3-ethyl-2,5-dimethylpyrazine, 2,3-diethyl-5-methylpyrazine, and 3,5-diethyl-2-methylpyrazine; other compounds identified were furans and aldehydes. More volatiles were generated in L-ascorbic acid with L-threonine systems than in L-ascorbic acid with L-serine systems studies showed that furans such as furfural, 2-furanmethanol, benzofuran, 2,5-furandicar-boxaldehyde and 2-furfurylfuran were formed mainly at acidic pH. In contrast, higher pH values could promote the production of pyrazines. (C) 2009 Elsevier Ltd. All rights reserved.
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表征谱图

  • 氢谱
    1HNMR
  • 质谱
    MS
  • 碳谱
    13CNMR
  • 红外
    IR
  • 拉曼
    Raman
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mass
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  • 峰位数据
  • 峰位匹配
  • 表征信息
Shift(ppm)
Intensity
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Assign
Shift(ppm)
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测试频率
样品用量
溶剂
溶剂用量
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