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顺式-1-(羟甲基)-2-甲基-2-(4-甲基-3-戊烯基)环丙烷 | 499155-10-1

中文名称
顺式-1-(羟甲基)-2-甲基-2-(4-甲基-3-戊烯基)环丙烷
中文别名
——
英文名称
cis-1-(hydroxymethyl)-2-methyl-2-(4-methyl-3-pentenyl)cyclopropane
英文别名
(+)-(2R,3S)-2,3-methano-3,7-dimethyl-6-octen-1-ol;[(1R,2S)-2-Methyl-2-(4-methylpent-3-en-1-yl)cyclopropyl]methanol;[(1R,2S)-2-methyl-2-(4-methylpent-3-enyl)cyclopropyl]methanol
顺式-1-(羟甲基)-2-甲基-2-(4-甲基-3-戊烯基)环丙烷化学式
CAS
499155-10-1
化学式
C11H20O
mdl
——
分子量
168.279
InChiKey
XVBJCXHXYYFQKZ-QWRGUYRKSA-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:
    65 °C(Press: 20 Torr)
  • 密度:
    0.898±0.06 g/cm3(Predicted)

计算性质

  • 辛醇/水分配系数(LogP):
    3.1
  • 重原子数:
    12
  • 可旋转键数:
    4
  • 环数:
    1.0
  • sp3杂化的碳原子比例:
    0.82
  • 拓扑面积:
    20.2
  • 氢给体数:
    1
  • 氢受体数:
    1

SDS

SDS:523569aab5b23f16ac0658ed6b2dfaa3
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反应信息

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文献信息

  • Cyclopropanated Aromachemicals
    申请人:Turin Luca
    公开号:US20070259042A1
    公开(公告)日:2007-11-08
    A compound of formula (I): wherein R is —CH 2 OH, —C(O)H, —C(OR 3 ) 2 H, —C(OR 4 )(OH)H, —CH═NC 6 H 4 C(O)OR 5 or —CH═NR 6 ; R 1 and R 2 are each independently H or CH 3 ; R 3 and R 4 are each independently H or a straight or branched aliphatic group having from 1 to 12 carbon atoms, or each R 3 is covalently linked to the other R 3 to form a cyclic acetal having from 1 to 4 carbon atoms; R 5 is H or a straight or branched aliphatic group, or a cyclic, heterocyclic or aromatic group having from 1 to 12 carbon atoms; and R 6 has at least 10 carbon atoms and is an aliphatic group or an aromatic group. Mixtures of these compounds, methods for their preparation, their use as perfume materials for application to a variety of substrates and their use in flavouring and in articles of manufacture is also provided.
    化合物的式子为(I):其中R为—CH2OH,—C(O)H,—C(OR3)2H,—C(OR4)(OH)H,—CH═NC6H4C(O)OR5或—CH═NR6; R1和R2各自独立地为H或CH3; R3和R4各自独立地为H或具有1至12个碳原子的直链或支链脂肪基,或每个R3与另一个R3共价连接以形成具有1至4个碳原子的环状缩醛; R5为H或直链或支链脂肪基,或具有1至12个碳原子的环状,杂环或芳香族基; 而R6至少有10个碳原子,是脂肪族基或芳香族基。还提供了这些化合物的混合物,其制备方法,其用作香料材料以应用于各种基质以及其在调味和制造物品中的使用。
  • Aromachemicals
    申请人:Turin Luca
    公开号:US20070276152A1
    公开(公告)日:2007-11-29
    A compound or mixture of compounds of formulae: wherein R 1 and R 2 are each independently H or CH 3 .
    一个化学式为的化合物或混合物:其中R1和R2分别独立地为H或CH3
  • Samarium-promoted cyclopropanation of allylic alcohols
    作者:Gary A. Molander、Lori S. Harring
    DOI:10.1021/jo00276a008
    日期:1989.7
  • Synthesis and odor description of optically active cyclopropanated analogues of geraniol, nerol, nor-leaf alcohol, and matsutake alcohol
    作者:Hiroki Asao、Hiroyuki Sakauchi、Shigefumi Kuwahara、Hiromasa Kiyota
    DOI:10.1016/j.tetasy.2007.02.007
    日期:2007.3
    Both enantiomers of cyclopropanated analogues of geraniol, nerol, nor-leaf alcohol, and matsutake alcohol were synthesized and their odor properties evaluated. Odor characters in enantiomeric pairs were similar in the geraniol series. The (+)-(2R,3S)-nerol derivative showed various odor aspects. From the results of nor-leaf alcohol derivatives, an interaction between the (2-re,3-re)-face of nor-leaf alcohol and the human olfactory receptor was suggested. The odor of (3R)-matsutake alcohol derivative was superior to the enantiomer. (c) 2007 Elsevier Ltd. All rights reserved.
  • CITRAL AND CITRONELLAL DERIVATIVES
    申请人:Turin Luca
    公开号:US20090016976A1
    公开(公告)日:2009-01-15
    Improved citral and citronellal derivatives, and fragrance and flavorings including the derivatives, that have a longer useful shelf life than citral and citronellal and/or fragrances and flavoring including citral and citronellal, are disclosed. In particular, the derivatives maintain the fragrance characteristics of citral and citronellal, while lowering the allergic properties, and lemony flavors and fragrances with a longer shelf-life than citral and citronellal, are disclosed. Also discovered are methods of making the derivatives, and articles of manufacture including the derivatives. The derivatives replace the aldehyde group in citral or citronellal with a hydroxy group. In one embodiment, the derivatives also replaced one or more double bonds in citral or the double bond in citronellal with a cyclopropyl group, which can be unsubstituted, or substituted with one or two alkyl, preferably methyl, groups, or with an oxirane or thiirane ring or combinations thereof. The alkyl groups in the cyclopropyl groups can optionally be substituted, for example, with electron donating groups, electron withdrawing groups, groups which increase the hydrophilicity or hydrophobicity, and the like. Examples of suitable articles of manufacture include candles, air fresheners, perfumes, disinfectant compositions, hypochlorite (bleach) compositions, beverages such as beer and soda, denture cleanser tablets and flavored orally-delivered products such as lozenges, candies, and the like.
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