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4-(乙酰基氧基)-7,8-二甲氧基-2-萘羧酸甲酯 | 31206-84-5

中文名称
4-(乙酰基氧基)-7,8-二甲氧基-2-萘羧酸甲酯
中文别名
——
英文名称
Methyl-4-acetoxy-7,8-dimethoxy-2-naphthoat
英文别名
methyl 4-acetoxy-7,8-dimethoxy2-naphthoate;4-(Acetyloxy)-7,8-dimethoxy-2-naphthalenecarboxylic acid methyl ester;methyl 4-acetyloxy-7,8-dimethoxynaphthalene-2-carboxylate
4-(乙酰基氧基)-7,8-二甲氧基-2-萘羧酸甲酯化学式
CAS
31206-84-5
化学式
C16H16O6
mdl
——
分子量
304.299
InChiKey
DVMOYFLANXQVCR-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):
    2.7
  • 重原子数:
    22
  • 可旋转键数:
    6
  • 环数:
    2.0
  • sp3杂化的碳原子比例:
    0.25
  • 拓扑面积:
    71.1
  • 氢给体数:
    0
  • 氢受体数:
    6

文献信息

  • PHOTOCHROMIC 2H-NAPHTHOPYRANS
    申请人:TRANSITIONS OPTICAL, INC.
    公开号:EP1963918A1
    公开(公告)日:2008-09-03
  • Photochromic 2H-naphthopyrans
    申请人:Chopra Anu
    公开号:US20070145337A1
    公开(公告)日:2007-06-28
    Described are photochromic 2H-naphtho[1,2-b]pyrans characterized by two adjacent moderate to strong electron donor substituents at the 7 and 8 positions, a moderate to strong electron withdrawing substituent at the 5 position, and at the 2 position, one substituent that is a weak electron donor and another substituent that is a weak to moderate electron donor. An optional substituent is located at the 6 position and each of the positions may have reactive substituents that enable the photochromic material to be more compatible with the host polymer. The selection and placement of the aforementioned substituents being done on the naphthopyran to demonstrate a lambda max of less than 490 nanometers in the Photochromic Performance Test. The selection and placement of substituents also enables the balancing of photochromic properties, such as the intensity, as measured in the Photochromic Performance Test. Also described are polymeric organic host materials that contain or that are coated with such naphthopyrans or combinations thereof with complementary photochromic compounds to produce photochromic articles such as ophthalmic lenses.
  • US4975463A
    申请人:——
    公开号:US4975463A
    公开(公告)日:1990-12-04
  • [EN] PHOTOCHROMIC 2H-NAPHTHOPYRANS<br/>[FR] COMPOSES 2H-NAPHTOPYRANNES PHOTOCHROMIQUES
    申请人:TRANSITIONS OPTICAL INC
    公开号:WO2007073463A1
    公开(公告)日:2007-06-28
    [EN] Described are photochromic 2H-naphtho[1,2-b]pyrans characterized by two adjacent moderate to strong electron donor substituents at the 7 and 8 positions, a moderate to strong electron withdrawing substituent at the 5 position, and at the 2 position, one substituent that is a weak electron donor and another substituent that is a weak to moderate electron donor. An optional substituent is located at the 6 position and each of the positions may have reactive substituents that enable the photochromic material to be more compatible with the host polymer. The selection and placement of the aforementioned substituents being done on the naphthopyran to demonstrate a lambda max of less than 490 nanometers in the Photochromic Performance Test. The selection and placement of substituents also enables the balancing of photochromic properties, such as the intensity, as measured in the Photochromic Performance Test. Also described are polymeric organic host materials that contain or that are coated with such naphthopyrans or combinations thereof with complementary photochromic compounds to produce photochromic articles such as ophthalmic lenses.
    [FR] L'invention concerne des composés 2H-naphto[1,2-b]pyrannes photochromiques caractérisés par deux substituants donneurs d'électron adjacents modérés à forts aux positions 7 et 8, un substituant accepteur d'électron modéré à fort en position 5, et, en position 2, un substituant qui est un faible donneur d'électron et un autre substituant qui est un donneur d'électron faible à modéré. Un substituant facultatif est prévu en position 6, et chacune des positions peut comporter des substituants réactifs qui rendent la matière photochromique plus compatible avec le polymère hôte. La sélection et le placement des substituants mentionnés est mise en oeuvre sur le naphtopyranne de sorte que celui-ci présente une valeur lambda maximale inférieure à 490 nanomètres dans le test d'efficacité photochromique. La sélection et le placement des substituants permet aussi d'équilibrer des propriétés photochromiques telles que l'intensité, mesurée par le test d'efficacité photochromique. L'invention concerne également des matières organiques polymères hôtes qui contiennent de tels naphtopyrannes ou sont revêtues de ceux-ci, ou des combinaisons de celles-ci avec des composés photochomiques complémentaires qui permettent de produire des articles photochromiques tels que des lentilles ophtalmiques.
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