摩熵化学
数据库官网
小程序
打开微信扫一扫
首页 分子通 化学资讯 化学百科 反应查询 关于我们
请输入关键词

(S)-2,3-dihydropyridine-2,6-dicarboxylic acid

中文名称
——
中文别名
——
英文名称
(S)-2,3-dihydropyridine-2,6-dicarboxylic acid
英文别名
(S)-2,3-dihydrodipicolinic acid;(2S)-2,3-dihydropyridine-2,6-dicarboxylic acid
(S)-2,3-dihydropyridine-2,6-dicarboxylic acid化学式
CAS
——
化学式
C7H7NO4
mdl
——
分子量
169.137
InChiKey
UWOCFOFVIBZJGH-YFKPBYRVSA-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):
    -0.1
  • 重原子数:
    12
  • 可旋转键数:
    2
  • 环数:
    1.0
  • sp3杂化的碳原子比例:
    0.29
  • 拓扑面积:
    87
  • 氢给体数:
    2
  • 氢受体数:
    5

文献信息

  • NON-AQUEOUS ELECTROLYTIC SOLUTION, ELECTROCHEMICAL ELEMENT USING SAME, AND ALKYNYL COMPOUND USED THEREFOR
    申请人:Abe Koji
    公开号:US20120301797A1
    公开(公告)日:2012-11-29
    The present invention provides an excellent nonaqueous electrolytic solution capable of improving low-temperature and high-temperature cycle properties and load characteristics after high-temperature charging storage, an electrochemical element using it, and an alkynyl compound used for it. The nonaqueous electrolytic solution of the present invention comprises containing at least one alkynyl compound represented by the following general formula (I) in an amount of from 0.01 to 10% by mass in the nonaqueous electrolytic solution. R 1 (O) n —X 1 —R 2 (I) (In the formula, X 1 represents a group —C(═O)—, a group —C(═O)—C(═O)—, a group —S(═O) 2 —, a group —P(═O) (—R 3 )—, or a group —X 2 —S(═O) 2 O—. R 1 represents an alkenyl group, a formyl group, an alkyl group, an acyl group, an arylcarbonyl, an alkanesulfonyl group, an alkynyloxysulfonyl group, an arylsulfonyl group, a dialkylphosphoryl group, an alkyl(alkoxy)phosphoryl group, or a dialkoxyphosphoryl group; R 2 represents an alkynyl group or an alkynyloxy group; R 3 represents an alkyl group, an alkenyl group, an alkynyl group, an aryl group, an alkoxy group, an alkenyloxy group, an alkynyloxy group, or an aryloxy group; n indicates 0 or 1.
    本发明提供了一种优秀的非电解质溶液,能够改善低温和高温循环性能以及高温充电存储后的负载特性,以及使用它的电化学元件和用于它的炔基化合物。本发明的非电解质溶液包括以下通式(I)表示的至少一种炔基化合物,其在非电解质溶液中的质量分数为0.01至10%。R1(O)n—X1—R2(I)(在式中,X1表示基团—C(═O)—,基团—C(═O)—C(═O)—,基团—S(═O)2—,基团—P(═O)(—R3)—,或基团—X2—S(═O)2O—。R1表示烯基基团,甲酰基团,烷基基团,酰基团,芳基羰基,烷烷基磺酰基,炔氧基磺酰基,芳基磺酰基,二烷基酰基,烷基(烷氧基)酰基,或二烷氧基酰基;R2表示炔基团或炔氧基团;R3表示烷基,烯基,炔基,芳基,烷氧基,烯氧基,炔氧基,或芳氧基;n表示0或1。
  • BIOLOGICAL SYNTHESIS OF DIFUNCTIONAL HEXANES AND PENTANES FROM CARBOHYDRATE FEEDSTOCKS
    申请人:Baynes Brian M.
    公开号:US20120301950A1
    公开(公告)日:2012-11-29
    Provided herein are methods for the production of difunctional alkanes in microorganisms. Also provided are enzymes and nucleic acids encoding such enzymes, associated with the difunctional alkane production from carbohydrates feedstocks in microorganisms. The invention also provides recombinant microorganisms and metabolic pathways for the production of difunctional alkanes.
    本文提供了在微生物中生产双官能基烷烃的方法。同时还提供了编码这种酶的核酸和酶,与从碳水化合物饲料中生产双官能基烷烃相关。本发明还提供了重组生物和代谢途径,用于生产双官能基烷烃
  • Biological Synthesis of Difunctional Hexanes and Pentanes from Carbohydrate Feedstocks
    申请人:Baynes Brain M.
    公开号:US20130017593A1
    公开(公告)日:2013-01-17
    Provided herein are methods for the production of difunctional alkanes in microorganisms. Also provided are enzymes and nucleic acids encoding such enzymes, associated with the difunctional alkane production from carbohydrates feedstocks in microorganisms. The invention also provides recombinant microorganisms and metabolic pathways for the production of difunctional alkanes.
    本文提供了在微生物中生产二官能烷的方法。同时还提供了编码这些酶的酶和核酸,这些酶与从碳水化合物饲料中生产二官能烷有关。本发明还提供了重组生物和代谢途径,用于生产二官能烷。
  • Engineered CO2 fixing microorganisms producing carbon-based products of interest
    申请人:Joule Unlimited Technologies, Inc.
    公开号:EP2706111A1
    公开(公告)日:2014-03-12
    The present disclosure identifies pathways and mechanisms to confer production of carbon-based products of interest such as ethanol, ethylene, chemicals, polymers, n-alkanes, isoprenoids, pharmaceutical products or intermediates thereof in photoautotrophic organisms such that these organisms efficiently convert carbon dioxide and light into carbon-based products of interest, and in particular the use of such organisms for the commercial production of ethanol, ethylene, chemicals, polymers, n-alkanes, isoprenoids, pharmaceutical products or intermediates thereof.
    本公开确定了在光自养生物体中生产乙醇乙烯化学品、聚合物、正烷烃、异戊烯、医药产品或其中间体等相关碳基产品的途径和机制,从而使这些生物体有效地将二氧化碳和光转化为相关碳基产品,特别是利用这些生物体进行乙醇乙烯化学品、聚合物、正烷烃、异戊烯、医药产品或其中间体的商业化生产。
  • Non-aqueous electrolytic solution, electrochemical element using the same and alkynyl compound used therefor
    申请人:Ube Industries, Ltd.
    公开号:EP2883867A2
    公开(公告)日:2015-06-17
    The present invention provides an excellent nonaqueous electrolytic solution capable of improving low-temperature and high-temperature cycle properties and load characteristics after high-temperature charging storage, an electrochemical element using it, and an alkynyl compound used for it. The nonaqueous electrolytic solution of the present invention comprises at least one alkynyl compound represented by the following general formula (I) in an amount of from 0.01 to 10% by mass in the nonaqueous electrolytic solution.          R1(O)n-X1-R2     (I) In the formula, X1 represents a group -C(=O)-, a group -S(=O)2-, or a group -P(=O)(-R3)-. R1 represents an alkenyl group having from 2 to 8 carbon atoms; R2 represents an alkynyl group having from 3 to 8 carbon atoms or an alkynyloxy group having from 3 to 8 carbon atoms; R3 represents an alkyl group, an alkenyl group, an alkynyl group, an aryl group, an alkoxy group, an alkenyloxy group, an alkynyloxy group, or an aryloxy group; n indicates 0 or 1.
    本发明提供了一种能够改善低温和高温循环特性以及高温充电储存后负载特性的优良非基电解溶液、使用该溶液的电化学元件以及用于该溶液的炔基化合物。 本发明的非基电解溶液包含至少一种由下式通式(I)表示的炔基化合物,其在非基电解溶液中的含量为 0.01 至 10%(按质量计)。 R1(O)n-X1-R2 (I) 式中,X1 代表基团-C(=O)-、基团-S(=O)2-或基团-P(=O)(-R3)-。R1 代表具有 2 至 8 个碳原子的烯基;R2 代表具有 3 至 8 个碳原子的炔基或具有 3 至 8 个碳原子的炔氧基;R3 代表烷基、烯基、炔基、芳基、烷氧基、烯氧基、炔氧基或芳氧基;n 表示 0 或 1。
查看更多

同类化合物

(甲基3-(二甲基氨基)-2-苯基-2H-azirene-2-羧酸乙酯) (±)-盐酸氯吡格雷 (±)-丙酰肉碱氯化物 (d(CH2)51,Tyr(Me)2,Arg8)-血管加压素 (S)-(+)-α-氨基-4-羧基-2-甲基苯乙酸 (S)-阿拉考特盐酸盐 (S)-赖诺普利-d5钠 (S)-2-氨基-5-氧代己酸,氢溴酸盐 (S)-2-[[[(1R,2R)-2-[[[3,5-双(叔丁基)-2-羟基苯基]亚甲基]氨基]环己基]硫脲基]-N-苄基-N,3,3-三甲基丁酰胺 (S)-2-[3-[(1R,2R)-2-(二丙基氨基)环己基]硫脲基]-N-异丙基-3,3-二甲基丁酰胺 (S)-1-(4-氨基氧基乙酰胺基苄基)乙二胺四乙酸 (S)-1-[N-[3-苯基-1-[(苯基甲氧基)羰基]丙基]-L-丙氨酰基]-L-脯氨酸 (R)-乙基N-甲酰基-N-(1-苯乙基)甘氨酸 (R)-丙酰肉碱-d3氯化物 (R)-4-N-Cbz-哌嗪-2-甲酸甲酯 (R)-3-氨基-2-苄基丙酸盐酸盐 (R)-1-(3-溴-2-甲基-1-氧丙基)-L-脯氨酸 (N-[(苄氧基)羰基]丙氨酰-N〜5〜-(diaminomethylidene)鸟氨酸) (6-氯-2-吲哚基甲基)乙酰氨基丙二酸二乙酯 (4R)-N-亚硝基噻唑烷-4-羧酸 (3R)-1-噻-4-氮杂螺[4.4]壬烷-3-羧酸 (3-硝基-1H-1,2,4-三唑-1-基)乙酸乙酯 (2S,4R)-Boc-4-环己基-吡咯烷-2-羧酸 (2S,3S,5S)-2-氨基-3-羟基-1,6-二苯己烷-5-N-氨基甲酰基-L-缬氨酸 (2S,3S)-3-((S)-1-((1-(4-氟苯基)-1H-1,2,3-三唑-4-基)-甲基氨基)-1-氧-3-(噻唑-4-基)丙-2-基氨基甲酰基)-环氧乙烷-2-羧酸 (2S)-2,6-二氨基-N-[4-(5-氟-1,3-苯并噻唑-2-基)-2-甲基苯基]己酰胺二盐酸盐 (2S)-2-氨基-N,3,3-三甲基-N-(苯甲基)丁酰胺 (2S)-2-氨基-3-甲基-N-2-吡啶基丁酰胺 (2S)-2-氨基-3,3-二甲基-N-(苯基甲基)丁酰胺, (2S)-2-氨基-3,3-二甲基-N-2-吡啶基丁酰胺 (2S,4R)-1-((S)-2-氨基-3,3-二甲基丁酰基)-4-羟基-N-(4-(4-甲基噻唑-5-基)苄基)吡咯烷-2-甲酰胺盐酸盐 (2R,3'S)苯那普利叔丁基酯d5 (2R)-2-氨基-3,3-二甲基-N-(苯甲基)丁酰胺 (2-氯丙烯基)草酰氯 (1S,3S,5S)-2-Boc-2-氮杂双环[3.1.0]己烷-3-羧酸 (1R,5R,6R)-5-(1-乙基丙氧基)-7-氧杂双环[4.1.0]庚-3-烯-3-羧酸乙基酯 (1R,4R,5S,6R)-4-氨基-2-氧杂双环[3.1.0]己烷-4,6-二羧酸 齐特巴坦 齐德巴坦钠盐 齐墩果-12-烯-28-酸,2,3-二羟基-,苯基甲基酯,(2a,3a)- 齐墩果-12-烯-28-酸,2,3-二羟基-,羧基甲基酯,(2a,3b)-(9CI) 黄酮-8-乙酸二甲氨基乙基酯 黄荧菌素 黄体生成激素释放激素(1-6) 黄体生成激素释放激素 (1-5) 酰肼 黄体瑞林 麦醇溶蛋白 麦角硫因 麦芽聚糖六乙酸酯 麦根酸