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

1-chloro-1,3,3-triphenylpropane | 70550-48-0

中文名称
——
中文别名
——
英文名称
1-chloro-1,3,3-triphenylpropane
英文别名
1-Chlor-1,3,3-triphenylpropan;(1-Chloro-3,3-diphenylpropyl)benzene
1-chloro-1,3,3-triphenylpropane化学式
CAS
70550-48-0
化学式
C21H19Cl
mdl
——
分子量
306.835
InChiKey
DKPVADYIAYWCGB-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):
    6.1
  • 重原子数:
    22
  • 可旋转键数:
    5
  • 环数:
    3.0
  • sp3杂化的碳原子比例:
    0.14
  • 拓扑面积:
    0
  • 氢给体数:
    0
  • 氢受体数:
    0

反应信息

点击查看最新优质反应信息

文献信息

  • Relative reactivities of alkenes toward the diphenylmethyl cation
    作者:Herbert Mayr、Rudolf Pock
    DOI:10.1016/s0040-4039(00)81869-9
    日期:——
    The relative reactivities of alkyl and phenyl substituted alkenes toward diphenylmethyl chloride/ZnCl2/Et2O in dichloromethane at −78°C have been determined by competition experiments. The transition state structure is discussed.
    通过竞争实验确定了烷基和苯基取代的烯烃在二氯甲烷中于-78℃下对二苯基甲基氯/ ZnCl 2 / Et 2 O的相对反应性。讨论了过渡状态结构。
  • NUCLEIC ACID, COMPOSITION AND CONJUGATE CONTAINING SAME, AND PREPARATION METHOD AND USE
    申请人:Suzhou Ribo Life Science Co., Ltd.
    公开号:EP3719125A1
    公开(公告)日:2020-10-07
    Provided are a siRNA for inhibiting the expression of hepatitis B virus gene, and a pharmaceutical composition and conjugate containing the siRNA. Each nucleotide in the siRNA is independently a modified nucleotide. The siRNA comprises a sense strand and an antisense strand. The sense strand of the siRNA comprises a nucleotide sequence 1 having the same length and no more than three nucleotides different from the nucleotide sequence shown in SEQ ID NO: 155, and the antisense strand of the siRNA comprises a nucleotide sequence 2 having the same length and no more than three nucleotides different from the nucleotide sequence shown in SEQ ID NO: 156.
    本文提供了一种用于抑制乙型肝炎病毒基因表达的 siRNA,以及含有该 siRNA 的药物组合物和共轭物。 siRNA 中的每个核苷酸都是独立的修饰核苷酸。 siRNA 包括有义链和反义链。 siRNA 的有义链包括与 SEQ ID NO: 155 所示核苷酸序列具有相同长度且相差不超过三个核苷酸的核苷酸序列 1,而 siRNA 的无义链包括与 SEQ ID NO: 156 所示核苷酸序列具有相同长度且相差不超过三个核苷酸的核苷酸序列 2。
  • NUCLEIC ACID, COMPOSITION AND CONJUGATE CONTAINING SAME, PREPARATION METHOD, AND USE
    申请人:Suzhou Ribo Life Science Co., Ltd.
    公开号:EP3719127A1
    公开(公告)日:2020-10-07
    The present disclosure provides a siRNA for inhibiting the expression of apolipoprotein C3 (ApoC3) gene, and a pharmaceutical composition and a conjugate comprising the siRNA; wherein each nucleotide in the siRNA is independently a modified nucleotide, and the siRNA comprises a sense strand and an antisense strand; the sense strand comprises a nucleotide sequence A, the nucleotide sequence A having the same length as the nucleotide sequence as represented by SEQ ID NO:1 with no more than 3 nucleotide differences; the antisense strand comprises a nucleotide sequence B, the nucleotide sequence B having the same length as the nucleotide sequence as represented by SEQ ID NO:2 with no more than 3 nucleotide differences.
    本发明公开了一种用于抑制载脂蛋白C3(ApoC3)基因表达的siRNA,以及包含该siRNA的药物组合物和共轭物;其中,该siRNA中的每个核苷酸都是独立的修饰核苷酸,该siRNA包括有义链和反义链;该有义链包括核苷酸序列A,该核苷酸序列A与SEQ ID NO:1 所代表的核苷酸序列具有相同的长度,但核苷酸差异不超过 3 个;反义链包括核苷酸序列 B,核苷酸序列 B 与 SEQ ID NO:2 所代表的核苷酸序列具有相同的长度,但核苷酸差异不超过 3 个。
  • NUCLEIC ACID, COMPOSITION AND CONJUGATE CONTAINING NUCLEIC ACID, PREPARATION METHOD AND USE
    申请人:Suzhou Ribo Life Science Co., Ltd.
    公开号:EP3718572A1
    公开(公告)日:2020-10-07
    Provided are an siRNA for inhibiting expression of a Hepatitis B virus gene, and a pharmaceutical composition and conjugate containing the siRNA. Each nucleotide in the siRNA is an independently modified or unmodified nucleotide; the siRNA comprises a sense strand and an antisense strand; the sense strand comprises a nucleotide sequence A; the length of the nucleotide sequence A is the same as that of a nucleotide sequence as shown in SEQ ID NO: 1, and the number of the nucleotide differences is not more than three; the antisense strand comprises a nucleotide sequence B; and the length of the nucleotide sequence B is the same as that of a nucleotide sequence as shown in SEQ ID NO: 2, and number of nucleotide differences is not more than three.
    本发明提供了一种用于抑制乙型肝炎病毒基因表达的 siRNA,以及含有该 siRNA 的药物组合物和共轭物。siRNA 中的每个核苷酸都是独立修饰或未修饰的核苷酸;siRNA 包括有义链和反义链;有义链包括核苷酸序列 A;核苷酸序列 A 的长度与 SEQ ID NO:1 所示的核苷酸序列相同,且核苷酸差异数目不超过三个;反义链包括核苷酸序列 B;核苷酸序列 B 的长度与 SEQ ID NO: 2 所示的核苷酸序列相同,且核苷酸差异数目不超过三个。
  • NUCLEIC ACID, COMPOSITION AND CONJUGATE CONTAINING NUCLEIC ACID, PREPARATION METHOD THEREFOR AND USE THEREOF
    申请人:Suzhou Ribo Life Science Co., Ltd.
    公开号:EP3719126A1
    公开(公告)日:2020-10-07
    Provided are a siRNA for inhibiting the expression of an angiopoietin-like protein 3 (ANGPTL3) gene, and a pharmaceutical composition and a conjugate comprising the siRNA; wherein each nucleotide in the siRNA is independently a modified or unmodified nucleotide, and the siRNA comprises a sense strand and an antisense strand; the sense strand comprises a nucleotide sequence A, the nucleotide sequence A having the same length as the nucleotide sequence as represented by SEQ ID NO:1 with no more than 3 nucleotide differences; the antisense strand comprises a nucleotide sequence B, the nucleotide sequence B having the same length as the nucleotide sequence as represented by SEQ ID NO:2 with no more than 3 nucleotide differences.
    提供了一种用于抑制血管生成素样蛋白3(ANGPTL3)基因表达的siRNA,以及包含该siRNA的药物组合物和共轭物;其中,siRNA中的每个核苷酸独立地为修饰或未修饰的核苷酸,且siRNA包括有义链和反义链;有义链包括核苷酸序列A,该核苷酸序列A与SEQ ID NO.1所代表的核苷酸序列具有相同的长度,且核苷酸差异不超过3个;反义链包括核苷酸序列B,该核苷酸序列B与SEQ ID NO:1所代表的核苷酸序列具有相同的长度,且核苷酸差异不超过3个;反义链包括核苷酸序列C,该核苷酸序列C与SEQ ID NO:1所代表的核苷酸序列具有相同的长度,且核苷酸差异不超过3个:1 所代表的核苷酸序列具有相同的长度,但核苷酸差异不超过 3 个;反义链包括核苷酸序列 B,核苷酸序列 B 与 SEQ ID NO:2 所代表的核苷酸序列具有相同的长度,但核苷酸差异不超过 3 个。
查看更多

同类化合物

(βS)-β-氨基-4-(4-羟基苯氧基)-3,5-二碘苯甲丙醇 (S,S)-邻甲苯基-DIPAMP (S)-(-)-7'-〔4(S)-(苄基)恶唑-2-基]-7-二(3,5-二-叔丁基苯基)膦基-2,2',3,3'-四氢-1,1-螺二氢茚 (S)-盐酸沙丁胺醇 (S)-3-(叔丁基)-4-(2,6-二甲氧基苯基)-2,3-二氢苯并[d][1,3]氧磷杂环戊二烯 (S)-2,2'-双[双(3,5-三氟甲基苯基)膦基]-4,4',6,6'-四甲氧基联苯 (S)-1-[3,5-双(三氟甲基)苯基]-3-[1-(二甲基氨基)-3-甲基丁烷-2-基]硫脲 (R)富马酸托特罗定 (R)-(-)-盐酸尼古地平 (R)-(-)-4,12-双(二苯基膦基)[2.2]对环芳烷(1,5环辛二烯)铑(I)四氟硼酸盐 (R)-(+)-7-双(3,5-二叔丁基苯基)膦基7''-[((6-甲基吡啶-2-基甲基)氨基]-2,2'',3,3''-四氢-1,1''-螺双茚满 (R)-(+)-7-双(3,5-二叔丁基苯基)膦基7''-[(4-叔丁基吡啶-2-基甲基)氨基]-2,2'',3,3''-四氢-1,1''-螺双茚满 (R)-(+)-7-双(3,5-二叔丁基苯基)膦基7''-[(3-甲基吡啶-2-基甲基)氨基]-2,2'',3,3''-四氢-1,1''-螺双茚满 (R)-(+)-4,7-双(3,5-二-叔丁基苯基)膦基-7“-[(吡啶-2-基甲基)氨基]-2,2”,3,3'-四氢1,1'-螺二茚满 (R)-3-(叔丁基)-4-(2,6-二苯氧基苯基)-2,3-二氢苯并[d][1,3]氧杂磷杂环戊烯 (R)-2-[((二苯基膦基)甲基]吡咯烷 (R)-1-[3,5-双(三氟甲基)苯基]-3-[1-(二甲基氨基)-3-甲基丁烷-2-基]硫脲 (N-(4-甲氧基苯基)-N-甲基-3-(1-哌啶基)丙-2-烯酰胺) (5-溴-2-羟基苯基)-4-氯苯甲酮 (5-溴-2-氯苯基)(4-羟基苯基)甲酮 (5-氧代-3-苯基-2,5-二氢-1,2,3,4-oxatriazol-3-鎓) (4S,5R)-4-甲基-5-苯基-1,2,3-氧代噻唑烷-2,2-二氧化物-3-羧酸叔丁酯 (4S,4''S)-2,2''-亚环戊基双[4,5-二氢-4-(苯甲基)恶唑] (4-溴苯基)-[2-氟-4-[6-[甲基(丙-2-烯基)氨基]己氧基]苯基]甲酮 (4-丁氧基苯甲基)三苯基溴化磷 (3aR,8aR)-(-)-4,4,8,8-四(3,5-二甲基苯基)四氢-2,2-二甲基-6-苯基-1,3-二氧戊环[4,5-e]二恶唑磷 (3aR,6aS)-5-氧代六氢环戊基[c]吡咯-2(1H)-羧酸酯 (2Z)-3-[[(4-氯苯基)氨基]-2-氰基丙烯酸乙酯 (2S,3S,5S)-5-(叔丁氧基甲酰氨基)-2-(N-5-噻唑基-甲氧羰基)氨基-1,6-二苯基-3-羟基己烷 (2S,2''S,3S,3''S)-3,3''-二叔丁基-4,4''-双(2,6-二甲氧基苯基)-2,2'',3,3''-四氢-2,2''-联苯并[d][1,3]氧杂磷杂戊环 (2S)-(-)-2-{[[[[3,5-双(氟代甲基)苯基]氨基]硫代甲基]氨基}-N-(二苯基甲基)-N,3,3-三甲基丁酰胺 (2S)-2-[[[[[((1S,2S)-2-氨基环己基]氨基]硫代甲基]氨基]-N-(二苯甲基)-N,3,3-三甲基丁酰胺 (2S)-2-[[[[[[((1R,2R)-2-氨基环己基]氨基]硫代甲基]氨基]-N-(二苯甲基)-N,3,3-三甲基丁酰胺 (2-硝基苯基)磷酸三酰胺 (2,6-二氯苯基)乙酰氯 (2,3-二甲氧基-5-甲基苯基)硼酸 (1S,2S,3S,5S)-5-叠氮基-3-(苯基甲氧基)-2-[(苯基甲氧基)甲基]环戊醇 (1S,2S,3R,5R)-2-(苄氧基)甲基-6-氧杂双环[3.1.0]己-3-醇 (1-(4-氟苯基)环丙基)甲胺盐酸盐 (1-(3-溴苯基)环丁基)甲胺盐酸盐 (1-(2-氯苯基)环丁基)甲胺盐酸盐 (1-(2-氟苯基)环丙基)甲胺盐酸盐 (1-(2,6-二氟苯基)环丙基)甲胺盐酸盐 (-)-去甲基西布曲明 龙蒿油 龙胆酸钠 龙胆酸叔丁酯 龙胆酸 龙胆紫-d6 龙胆紫