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

methyl 1,4-dithia-5,8-diselenafulvalen-2-carboxylate | 135418-83-6

中文名称
——
中文别名
——
英文名称
methyl 1,4-dithia-5,8-diselenafulvalen-2-carboxylate
英文别名
Methyl 2-(1,3-diselenol-2-ylidene)-1,3-dithiole-4-carboxylate
methyl 1,4-dithia-5,8-diselenafulvalen-2-carboxylate化学式
CAS
135418-83-6
化学式
C8H6O2S2Se2
mdl
——
分子量
356.186
InChiKey
FHWMYLDACCCWHY-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):
    1.5
  • 重原子数:
    14
  • 可旋转键数:
    2
  • 环数:
    2.0
  • sp3杂化的碳原子比例:
    0.12
  • 拓扑面积:
    76.9
  • 氢给体数:
    0
  • 氢受体数:
    4

反应信息

  • 作为产物:
    描述:
    1,3-diselenole-2-selone2-oxo-1,3-dithiol-4-carboxylic acid methyl ester三苯基膦 作用下, 以 为溶剂, 以9.2%的产率得到methyl 1,4-dithia-5,8-diselenafulvalen-2-carboxylate
    参考文献:
    名称:
    Thia-and/or selenafulvalenyl group-containing compound
    摘要:
    具有以下结构的含有thia-和/或selenafulvalenyl基团的化合物(I):其中X.sub.1、X.sub.2、X.sub.3、X.sub.4、X'.sub.1、X'.sub.2、X'.sub.3和X'.sub.4中的每一个独立地是S或Se,Y是一个具有不会妨碍分子重叠的大小的电子给予或电子接受基团,m是0到4的整数,Z.sub.1、Z.sub.2、Z'.sub.1和Z'.sub.2中的每一个独立地是氢原子,C.sub.n H.sub.2n+1,其中n是1到5的整数,或者,Z.sub.1与Z.sub.2和Z'.sub.1与Z'.sub.2的组合是C.sub.n H.sub.2n,其中n是1到5的整数,或X(C.sub.n H.sub.2n).sub.n',其中X是S或Se,n'是1到3的整数,R.sub.1、R.sub.2、R.sub.3、R'.sub.1、R'.sub.2和R'.sub.3中的每一个独立地是氢原子或C.sub.n H.sub.2n+1,其中n是1到5的整数。该化合物具有电子给予性质,可用于制备电导性复合物。该化合物具有出色的热稳定性。
    公开号:
    US05175280A1
点击查看最新优质反应信息

文献信息

  • Thia-and/or selenafulvalenyl group-containing compound
    申请人:Idemitsu Kosan Co., Ltd.
    公开号:US05175280A1
    公开(公告)日:1992-12-29
    A thia- and/or selenafulvalenyl group-containing compound of the formula (I), ##STR1## wherein each of X.sub.1, X.sub.2, X.sub.3, X.sub.4, X'.sub.1, X'.sub.2, X'.sub.3 and X'.sub.4 is independently S or Se, Y is an electron donating or electron accepting group having a size which is not so large as to prevent molecular overlapping, m is an integer of 0 to 4, each of Z.sub.1, Z.sub.2, Z'.sub.1 and Z'.sub.2 is independently a hydrogen atom, C.sub.n H.sub.2n+1 in which n is an integer of 1 to 5, or alternatively, a combination of Z.sub.1 with Z.sub.2 and Z'.sub.1 with Z'.sub.2 is C.sub.n H.sub.2n in which n is an integer of 1 to 5, or X(C.sub.n H.sub.2n).sub.n', X in which X is S or Se and n' is an integer of 1 to 3, and each of R.sub.1, R.sub.2, R.sub.3, R'.sub.1, R'.sub.2 and R'.sub.3 is independently a hydrogen atom or C.sub.n H.sub.2n+1 in which n is an integer of 1 to 5. The compound has an electron donating nature and can be used to make electrically conductive complexes. The compound has an excellent thermal stability.
    具有以下结构的含有thia-和/或selenafulvalenyl基团的化合物(I):其中X.sub.1、X.sub.2、X.sub.3、X.sub.4、X'.sub.1、X'.sub.2、X'.sub.3和X'.sub.4中的每一个独立地是S或Se,Y是一个具有不会妨碍分子重叠的大小的电子给予或电子接受基团,m是0到4的整数,Z.sub.1、Z.sub.2、Z'.sub.1和Z'.sub.2中的每一个独立地是氢原子,C.sub.n H.sub.2n+1,其中n是1到5的整数,或者,Z.sub.1与Z.sub.2和Z'.sub.1与Z'.sub.2的组合是C.sub.n H.sub.2n,其中n是1到5的整数,或X(C.sub.n H.sub.2n).sub.n',其中X是S或Se,n'是1到3的整数,R.sub.1、R.sub.2、R.sub.3、R'.sub.1、R'.sub.2和R'.sub.3中的每一个独立地是氢原子或C.sub.n H.sub.2n+1,其中n是1到5的整数。该化合物具有电子给予性质,可用于制备电导性复合物。该化合物具有出色的热稳定性。
查看更多

同类化合物

甲酰四硫富瓦烯 环己酮,2-[二(甲硫基)亚甲基]- 5-乙基-2-甲基-噻吩-3-酮 4-羟基-2,5-二甲基噻吩-3(2H)-酮 4-乙基硫烷基-丁-3-烯-2-酮 4,4-二甲基-1,1-双(甲基硫代)-1-戊烯-3-酮 3-[双(甲基磺酰基)亚甲基]-2,4-戊二酮 3,3-双(甲硫基)-2-氰基丙烯酸乙酯 2-氰基-3,3-双(甲基硫代)丙烯酰胺 2-氰-3,3-二(甲硫基)丙烯酸甲酯 2-氯-3-氧代-2,3-二氢-2-噻吩羧酸甲酯 2-氨基-4,5-二氢-3-噻吩甲酰胺 2-乙酰基-3-氨基-3-甲基硫代丙烯腈 2-丙烯酸,3-(十六烷基硫代)-,甲基酯,(Z)- 2-(环丙基羰基)-3,3-二(甲基硫代)丙烯腈 2-(1,3-二噻戊环-2-亚基)环戊酮 2-(1,3-二噻戊环-2-亚基)环己酮 2,2-二甲基噻吩-3-酮 1-己烯-3-酮,1,1-二(甲硫基)-2-硝基- 1,3-二硫杂环戊烯-4-羧酸 (3Z)-1,1,1-三氟-4-(甲硫基)-3-丁烯-2-酮 (3E)-4-(甲硫基)-3-戊烯-2-酮 (2Z)-[3-(2-溴乙基)-4-氧代-1,3-噻唑烷-2-亚基]乙酸乙酯 (2Z)-2-(3-乙基-4-氧代-1,3-噻唑烷-2-亚基)乙酸乙酯 (2Z)-(3-甲基-4-氧代-1,3-噻唑烷-2-亚基)乙酸乙酯 (2E)-2-(4-氧代噻唑烷-2-亚基)乙酸丁酯 2-[bis(methylthio)methylene]-5-([13C]-methyl)cyclohexanone 2-Cyan-2-(2,3,4,5,6,7-hexahydrobenzothiazol-2-yliden)essigsaeuremethylester 2-(chlorodifluoromethylcarbonylmethylene)-1,3-thiazolidine 2,3-bis((S)-2-dodecyloxy-propanylthio)-6-(carboxy)tetrathiafulvalene 3-Amino-2-cyan-3-(ethylthio)acrylsaeuremethylester 5-dimethylaminomethylene-3-ethoxycarbonyl-2-methyl-4-oxo-4,5-dihydrothiophene 2-(1-methoxycarbonyl)trifluoroethylidene-1,3-dithiolane 2-(1-methoxycarbonyl)trifluoroethylidene-1,3-oxathiolane (Z)-4-(1-Butylthio)-but-3-en-2-one methyl 3-(butylthio)acrylate 3-Methylamino-3-methylmercapto-2-cyan-acrylsaeure-methylester 2-sec-butoxy-3,5-dimethylthiotetronic acid ethyl 2-amino-4-hydroxy-5-methyl-4-(trifluoromethyl)-4,5-dihydrothiophene-3-carboxylate cyano-(3-ethyl-4-oxo-thiazolidin-2-yliden)-acetic acid allyl ester 2‑(3,3‑dimethyl‑2‑oxobutylidene)‑1,3‑thiazolidin‑4‑one isopropyl 1,3-dithiol-2-ylidenemethylsulfonylacetate (E)-5-(furan-2-yl)-1,1-bis(methylthio)penta-1,4-dien-3-one ethyl 3-cyclohexylamino-3-methylthio-2-cyanoacrylate ethyl 2-ethoxy-4,5-dihydrothiophene-3-carboxylate 2,4-dimethyl-2,3-dihydro-thiophen-3-one isopropyl 2-(1,3-dithiol-2-ylidene)-2-(N-cyclohexylcarbamoyl)acetate 4,4-bis(methylthio)but-3-en-2-one-1,1,1,3-d4 N-(2-aminoethyl)-benzo[b]thieno[2,3-c]pyridine-3-carboamide.hydrochloride 3-(1,3-dithiolan-2-ylidene)butan-2-one