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3-Isocyanato-6-[(4-isocyanato-2,2,3,3,4,5,5,6,6-nonamethylcyclohexyl)methyl]-1,1,2,2,3,4,4,5,5-nonamethylcyclohexane

中文名称
——
中文别名
——
英文名称
3-Isocyanato-6-[(4-isocyanato-2,2,3,3,4,5,5,6,6-nonamethylcyclohexyl)methyl]-1,1,2,2,3,4,4,5,5-nonamethylcyclohexane
英文别名
3-isocyanato-6-[(4-isocyanato-2,2,3,3,4,5,5,6,6-nonamethylcyclohexyl)methyl]-1,1,2,2,3,4,4,5,5-nonamethylcyclohexane
3-Isocyanato-6-[(4-isocyanato-2,2,3,3,4,5,5,6,6-nonamethylcyclohexyl)methyl]-1,1,2,2,3,4,4,5,5-nonamethylcyclohexane化学式
CAS
——
化学式
C33H58N2O2
mdl
——
分子量
514.8
InChiKey
IHBPYAPCMZERIL-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):
    12.3
  • 重原子数:
    37
  • 可旋转键数:
    4
  • 环数:
    2.0
  • sp3杂化的碳原子比例:
    0.94
  • 拓扑面积:
    58.9
  • 氢给体数:
    0
  • 氢受体数:
    4

文献信息

  • SILANE END CAPPED SUBSTITUTED UREA RESINS AND COATINGS THEREOF
    申请人:Webb Arthur A.
    公开号:US20140249273A1
    公开(公告)日:2014-09-04
    The below compound, which may be made by reacting a 3-trialkoxysilylpropyl amine with an acrylic acid ester, a methacrylic acid ester, a diester of maleic acid, a diester of fumaric acid, or acrylonitrile to form a secondary amino propylalkoxysilane, and reacting the secondary amino propylalkoxysilane with an isocyanate. R 1 is an alkyl group, X is —CHR 3 —CHR 4 —CO—O—R 2 or —CH 2 —CH 2 —CN, R 2 is an organic group, R 3 is —H or —CO—O—R 2 , R 4 is —H or —CH 3 , but R 4 is —H if R 3 is —CO—O—R 2 , R 5 is an aliphatic group or a residue of hexamethylene diisocyanate cyclic trimer or hexamethylene diisocyanate cyclic dimer, and n is 2 or 3. The below compound, which may be made by reacting a 3-trialkoxysilylpropyl amine with acrylonitrile. R 1 is an alkyl group.
  • US20140272437A1
    申请人:——
    公开号:US20140272437A1
    公开(公告)日:2014-09-18
  • [EN] SILANE END CAPPED SUBSTITUTED UREA RESINS AND COATINGS THEREOF<br/>[FR] RÉSINES D'URÉE SUBSTITUÉES COIFFÉES PAR SILANE ET REVÊTEMENTS CORRESPONDANTS
    申请人:US GOVERNMENT
    公开号:WO2014137694A1
    公开(公告)日:2014-09-12
    The compound below. R1 is an alkyl group or -(SiR72-O)m-R8. R7 is an alkoxy group. The value m is a nonnegative integer. R8 is an alkyl group or R3 and R4 are organic groups. R5 is an aliphatic group or a residue of a homopolymer of an aliphatic polyisocyanate. R6 has an electron withdrawing group that is bound to a carbon atom that is bound to the CHR4 group. The value n is an integer greater than or equal to 2. A method of: reacting a 3-trialkoxysilylpropyl amine with an organic compound having a carbon-carbon double bond activated by an electron withdrawing group to form a secondary amino propylalkoxysilane, and reacting the secondary amino propylalkoxysilane with an aliphatic polyisocyanate or a polymer thereof.
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同类化合物

(5β,6α,8α,10α,13α)-6-羟基-15-氧代黄-9(11),16-二烯-18-油酸 (3S,3aR,8aR)-3,8a-二羟基-5-异丙基-3,8-二甲基-2,3,3a,4,5,8a-六氢-1H-天青-6-酮 (2Z)-2-(羟甲基)丁-2-烯酸乙酯 (2S,4aR,6aR,7R,9S,10aS,10bR)-甲基9-(苯甲酰氧基)-2-(呋喃-3-基)-十二烷基-6a,10b-二甲基-4,10-dioxo-1H-苯并[f]异亚甲基-7-羧酸盐 (1aR,4E,7aS,8R,10aS,10bS)-8-[((二甲基氨基)甲基]-2,3,6,7,7a,8,10a,10b-八氢-1a,5-二甲基-氧杂壬酸[9,10]环癸[1,2-b]呋喃-9(1aH)-酮 (+)顺式,反式-脱落酸-d6 龙舌兰皂苷乙酯 龙脑香醇酮 龙脑烯醛 龙脑7-O-[Β-D-呋喃芹菜糖基-(1→6)]-Β-D-吡喃葡萄糖苷 龙牙楤木皂甙VII 龙吉甙元 齿孔醇 齐墩果醛 齐墩果酸苄酯 齐墩果酸甲酯 齐墩果酸溴乙酯 齐墩果酸二甲胺基乙酯 齐墩果酸乙酯 齐墩果酸3-O-alpha-L-吡喃鼠李糖基(1-3)-beta-D-吡喃木糖基(1-3)-alpha-L-吡喃鼠李糖基(1-2)-alpha-L-阿拉伯糖吡喃糖苷 齐墩果酸 beta-D-葡萄糖酯 齐墩果酸 beta-D-吡喃葡萄糖基酯 齐墩果酸 3-乙酸酯 齐墩果酸 3-O-beta-D-葡吡喃糖基 (1→2)-alpha-L-吡喃阿拉伯糖苷 齐墩果酸 齐墩果-12-烯-3b,6b-二醇 齐墩果-12-烯-3,24-二醇 齐墩果-12-烯-3,21,23-三醇,(3b,4b,21a)-(9CI) 齐墩果-12-烯-3,21,23-三醇,(3b,4b,21a)-(9CI) 齐墩果-12-烯-3,11-二酮 齐墩果-12-烯-2α,3β,28-三醇 齐墩果-12-烯-29-酸,3,22-二羟基-11-羰基-,g-内酯,(3b,20b,22b)- 齐墩果-12-烯-28-酸,3-[(6-脱氧-4-O-b-D-吡喃木糖基-a-L-吡喃鼠李糖基)氧代]-,(3b)-(9CI) 齐墩果-12-烯-28-酸,3,7-二羰基-(9CI) 齐墩果-12-烯-28-酸,3,21,29-三羟基-,g-内酯,(3b,20b,21b)-(9CI) 鼠特灵 鼠尾草酸醌 鼠尾草酸 鼠尾草酚酮 鼠尾草苦内脂 黑蚁素 黑蔓醇酯B 黑蔓醇酯A 黑蔓酮酯D 黑海常春藤皂苷A1 黑檀醇 黑果茜草萜 B 黑五味子酸 黏黴酮 黏帚霉酸