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1,2,3,4-Tetrabromo-5-[1,4-dibromo-2,2-bis[bromo-(2,3,4,5-tetrabromophenyl)methyl]-3,3-diphenyl-4-(2,3,4,5-tetrabromophenyl)butyl]benzene

中文名称
——
中文别名
——
英文名称
1,2,3,4-Tetrabromo-5-[1,4-dibromo-2,2-bis[bromo-(2,3,4,5-tetrabromophenyl)methyl]-3,3-diphenyl-4-(2,3,4,5-tetrabromophenyl)butyl]benzene
英文别名
1,2,3,4-tetrabromo-5-[1,4-dibromo-2,2-bis[bromo-(2,3,4,5-tetrabromophenyl)methyl]-3,3-diphenyl-4-(2,3,4,5-tetrabromophenyl)butyl]benzene
1,2,3,4-Tetrabromo-5-[1,4-dibromo-2,2-bis[bromo-(2,3,4,5-tetrabromophenyl)methyl]-3,3-diphenyl-4-(2,3,4,5-tetrabromophenyl)butyl]benzene化学式
CAS
——
化学式
C42H18Br20
mdl
——
分子量
2120.7
InChiKey
RQVRXEVFNBDVEK-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):
    24
  • 重原子数:
    62
  • 可旋转键数:
    11
  • 环数:
    6.0
  • 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

文献信息

  • PREPARATION OF BROMINE-CONTAINING AROMATIC COMPOUNDS AND THEIR APPLICATION AS FLAME RETARDANTS
    申请人:BROMINE COMPOUNDS LTD.
    公开号:US20150329447A1
    公开(公告)日:2015-11-19
    The invention relates to compounds of the formula Ar(—CH2C6Br5)y, wherein Ar indicates a structure comprising one or more six-membered aromatic ring(s) and —CH 2 C 6 Br 5 indicates a pentabromobenzyl group, characterized in that at least one carbon atom of said six-membered aromatic ring(s) is bonded to the benzylic carbon of said —CH 2 C 6 Br 5 group, wherein y, which indicates the number of the —CH 2 C 6 Br 5 groups in said compound, is not less than 1. Processes for preparing the compounds and their use as flame retardants are also disclosed.
    该发明涉及公式 Ar(—CH2C6Br5)y 的化合物,其中 Ar 表示一个结构,包括一个或多个六元芳环,—CH2C6Br5 表示一个五溴苄基团,其特征在于所述六元芳环中至少有一个碳原子与所述—CH2C6Br5基团的苄基碳键合,其中 y 表示所述化合物中—CH2C6Br5基团的数量不少于1。还公开了制备该化合物的方法以及其用作阻燃剂的用途。
  • US9481621B2
    申请人:——
    公开号:US9481621B2
    公开(公告)日:2016-11-01
  • US9988332B2
    申请人:——
    公开号:US9988332B2
    公开(公告)日:2018-06-05
  • [EN] PREPARATION OF BROMINE-CONTAINING AROMATIC COMPOUNDS AND THEIR APPLICATION AS FLAME RETARDANTS<br/>[FR] PRÉPARATION DE COMPOSÉS AROMATIQUES CONTENANT DU BROME ET LEUR APPLICATION COMME IGNIFUGEANTS
    申请人:BROMINE COMPOUNDS LTD
    公开号:WO2014106841A1
    公开(公告)日:2014-07-10
    The invention relates to compounds of the formula Ar(- CH2C6Br5)y, wherein Ar indicates a structure comprising one or more six-membered aromatic ring(s) and -CH2C6Br5 indicates a pentabromobenzyl group, characterized in that at least one carbon atom of said six-membered aromatic ring(s) is bonded to the benzylic carbon of said -CH2C6Br5 group, wherein y, which indicates the number of the -CH2C6Br5 groups in said compound, is not less than 1. Processes for preparing the compounds and their use as flame retardants are also disclosed.
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同类化合物

苯基(2,4,5-三苯基-2-环戊烯-1-基)甲酮 肠二醇 珠子草素 开环异落叶松树脂酚 安五脂素 外消旋肠二醇-13C3 去甲二氢愈创木酸 半去甲二氢愈创木酸 二甲基2,5-二苯基-3,4-二氢-2H-吡咯-3,4-二羧酸酯 二氢荜澄茄脂素 9,9'-二-O-(E)-阿魏酰开环异落叶松脂素 4-[4-(4-羟基-3-甲氧基苯基)-2,3-二甲基丁基]-2-甲氧基苯酚 2,6-二甲氧基-4-羟基苯甲醛 2,6-二甲氧基-4-[(2R,3R)-4-甲氧基-3-[(7-甲氧基-1,3-苯并二噁唑-5-基)甲基]-2-(甲氧基甲基)丁基]苯酚 2,3-双[(4-羟基-3-甲氧基苯基)甲基]丁烷-1,4-二醇 2,3-双[(3,4-二甲氧基苯基)甲基]丁烷-1,4-二醇 2,3-双[(3,4-二甲氧基苯基)甲基]丁二酸 2,3-双(4-羟基-3-甲氧基苄基)琥珀酸二甲酯 2,3-双(3,4-二甲氧基苄基)-4-甲氧基-4-氧代丁酸 2,3-二苄基丁烷-1,4-二醇 2,3-二甲基-1,4-二苯基丁烷-2,3-二醇 2,3-二甲基-1,4-二苯基丁烷-1,4-二酮 2,3-二异丙基-1,2-二苯基-1,4-丁二酮 2,3-二[(3-羟基苯基)甲基]丁烷-1,4-二醇 2,2,3,3-四甲基-1,4-二苯基丁烷-1,4-二酮 1,4-丁烷二酮 1,2,3,4-四苯基环戊烷 1,2,3,4-四苯基丁烷 1,2,3,4-四苯基-1,4-丁烷二酮 1,2,3,4-四-(4-甲氧基-苯基)-丁烷-1,4-二酮 1,1'-[(2S,3S)-2,3-双(甲氧基甲基)-1,4-丁二基]双[3,4-二甲氧基苯] 1,1'-(2,3-二甲基-1,4-丁烷二基)二(3,4-二甲氧基苯) 1,1',2,2',3,3'-六苯基-1,1'-联(2-环丙烯) (3,3,4,4-四甲基-2-苯基环丁烯-1-基)苯 (2R,3S)-1,4-二(4-羟基-3-甲氧基苯基)-2,3-二甲基丁烷-1-酮 (-)-二氢愈创木脂酸 (+)-开环异落叶松树脂酚 1,4-difluoro-1,2,34,-tetrahydrophenylbutane (1R*,2R*,3R*,4S*)-2,3-bis(hydroxymethyl)-1-(3,4-dimethoxyphenyl)-4-<3,4-(methylenedioxy)phenyl>butane-1,4-diol 2,5-diphenyl-3,4-dimethylhexa-1,5-diene meso-1,4-bis-(3,4-dihydroxyphenyl)-2,3-dimethylbutane bis-cyclic carbonate (2R,3R)-2-(4'-hydroxy-3'-methoxybenzyl)-3-(3'',4''-dimethoxybenzyl)-4-hydroxy-N-benzylbutyramide (2R,3R)-2-(3',4'-dihydroxybenzyl)-3-(3'',4''-dimethoxybenzyl)-4-hydroxy-N-benzylbutyramide 2,5-di(3-nitrophenyl)-3,3,4,4-tetracyanopyrrolidine 4,5-dihydroxy-2,4,5-triphenyl-3-(2-pyridyl)-1-pyrroline (+/-)-(1R,2S,3R,4R)-2,3-bis(hydroxymethyl)-1,4-bisphenyl-2-hydroxybutane-1,4-diol α,β-dimethyl-γ-phenylbutyrophenone meso-2,3-bis(3,4-dihydroxybenzyl)succinic acid (±)-1-(4-hydroxy-3-methoxyphenyl)-(2R,3S)-dimethyl-4-[3-methoxy-4-(picolinoyloxy)phenyl]butane meso-1,4-bis[3-methoxy-4-(picolinoyloxy)phenyl]-(2R,3S)-dimethylbutane