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3-[3-[4,4-二甲基-3-(环氧乙烷-2-基甲基)-2,5-二氧代咪唑烷-1-基]-2-(环氧乙烷-2-基甲氧基)丙基]-5,5-二甲基-1-(环氧乙烷-2-基甲基)咪唑烷-2,4-二酮 | 38304-52-8

中文名称
3-[3-[4,4-二甲基-3-(环氧乙烷-2-基甲基)-2,5-二氧代咪唑烷-1-基]-2-(环氧乙烷-2-基甲氧基)丙基]-5,5-二甲基-1-(环氧乙烷-2-基甲基)咪唑烷-2,4-二酮
中文别名
——
英文名称
1,3-Bis(1-glycidyl-5,5-dimethyl-hydantoin-3-yl)-2-propyl-2-glycidylether
英文别名
5,5,5',5'-tetramethyl-1,1'-bis-oxiranylmethyl-3,3'-(2-oxiranylmethoxy-propane-1,3-diyl)-bis-imidazolidine-2,4-dione;3,3'-[2-(oxiranylmethoxy)propane-1,3-diyl]bis[5,5-dimethyl-1-(oxiranylmethyl)imidazolidine-2,4-dione];1,3-Bis(5,5-dimethyl-1-glycidylhydantoin-3-yl)-2-glycidyloxypropane;3-[3-[4,4-dimethyl-3-(oxiran-2-ylmethyl)-2,5-dioxoimidazolidin-1-yl]-2-(oxiran-2-ylmethoxy)propyl]-5,5-dimethyl-1-(oxiran-2-ylmethyl)imidazolidine-2,4-dione
3-[3-[4,4-二甲基-3-(环氧乙烷-2-基甲基)-2,5-二氧代咪唑烷-1-基]-2-(环氧乙烷-2-基甲氧基)丙基]-5,5-二甲基-1-(环氧乙烷-2-基甲基)咪唑烷-2,4-二酮化学式
CAS
38304-52-8
化学式
C22H32N4O8
mdl
——
分子量
480.518
InChiKey
RXBBSTXUVVVWRC-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

物化性质

  • 沸点:
    578.55°C (rough estimate)
  • 密度:
    1.3311 (rough estimate)

计算性质

  • 辛醇/水分配系数(LogP):
    -1.4
  • 重原子数:
    34
  • 可旋转键数:
    11
  • 环数:
    5.0
  • sp3杂化的碳原子比例:
    0.82
  • 拓扑面积:
    128
  • 氢给体数:
    0
  • 氢受体数:
    8

文献信息

  • [EN] SULFONIUM DERIVATIVES AND THE USE THEROF AS LATENT ACIDS<br/>[FR] DÉRIVÉS DE SULFONIUM ET LEUR UTILISATION EN TANT QU'ACIDES LATENTS
    申请人:BASF SE
    公开号:WO2010046240A1
    公开(公告)日:2010-04-29
    Compounds of the formula (I), wherein Ar1 is for example phenylene or biphenylene both unsubstituted or substituted; Ar2 and Ar3 are for example independently of each other phenyl, naphthyl, biphenylylyl or heteroaryl, all optionally substituted; or Ar1 and Ar2 for example together with a direct bond, O, S or (CO), form a fused ring system; R is for example hydrogen, C3-C30cycloalkyl or C1-C18alkyl; and R1, R2 and R3 independently of each other are for example C1-C10haloalkyl; are effective photoacid generators (PAG).
    化合物的公式(I),其中Ar1例如是未取代或取代的苯基或联苯基; Ar2和Ar3例如是独立的苯基,萘基,联苯基或杂环基,均可选取代; 或者例如Ar1和Ar2与直接键,O,S或(CO)一起形成融合的环系统; R例如是氢,C3-C30环烷基或C1-C18烷基; R1,R2和R3独立地例如是C1-C10卤代烷基; 是有效的光酸发生剂(PAG)。
  • [EN] SULPHONIUM SALT INITIATORS<br/>[FR] INITIATEURS À BASE DE SELS DE SULFONIUM
    申请人:CIBA HOLDING INC
    公开号:WO2009047151A1
    公开(公告)日:2009-04-16
    Compounds of the formula (I), wherein X is a single bond, CRaRb O, S, NRC, NCORC, CO, SO or SO2; L, L1, L2, L3, L4, L5, L6, L7 and L8 are for example hydrogen, R1 or COT; T denotes T1 or O-T2; T1 and T2 for example are hydrogen, C1-C20alkyl, C3-C12cycloalkyl, C2-C20alkenyl, C5- C12cycloalkenyl, C6-C14aryl, C3-C12heteroaryl, C1-C20alkyl substituted by one or more D, C2- C20alkyl interrupted by one or more E, C2-C20alkyl substituted by one or more D and inter- rupted by one or more E or Q; R1, R2, R3, R4, Ra, Rb and Rc are T1; D is for example R5, OR5, SR5 or Q1; E is for example O, S, COO or Q2; R5 and R6 for example are hydrogen, C1- C12alkyl or phenyl; Q is for example C6-C12bicycloalkyl, C6-C12bicycloalkenyl or C6- C12tricycloalkyl; Q1 is for example, C6-C14aryl or C3-C12heteroaryl; Q2 is for example C6- C14arylene or C3-C12heteroarylene; Y is an anion; and M is a cation; provided that at least one of L, L1, L2, L3, L4, L5, L6, L7 and L8 is other than hydrogen; and provided that (i) at least one of T1 or T2 is a group Q; or (ii) at least one D is a group Q1; or (iii) at least one E is a group Q2; are suitable as photolatent catalysts.
    化合物的式子(I),其中X是单键,CRaRb O,S,NRC,NCORC,CO,SO或SO2; L,L1,L2,L3,L4,L5,L6,L7和L8例如是氢,R1或COT; T表示T1或O-T2; T1和T2例如是氢,C1-C20烷基,C3-C12环烷基,C2-C20烯基,C5-C12环烯基,C6-C14芳基,C3-C12杂芳基,被一个或多个D取代的C1-C20烷基,被一个或多个E中断的C2-C20烷基,被一个或多个D取代并被一个或多个E或Q中断的C2-C20烷基; R1,R2,R3,R4,Ra,Rb和Rc是T1; D例如是R5,OR5,SR5或Q1; E例如是O,S,COO或Q2; R5和R6例如是氢,C1-C12烷基或苯基; Q例如是C6-C12双环烷基,C6-C12双环烯基或C6-C12三环烷基; Q1例如是C6-C14芳基或C3-C12杂芳基; Q2例如是C6-C14芳撑基或C3-C12杂芳撑基; Y是阴离子; M是阳离子; 前提是L,L1,L2,L3,L4,L5,L6,L7和L8中至少有一个不是氢; 并且前提是(i)至少有一个T1或T2是Q组; 或(ii)至少有一个D是Q1组; 或(iii)至少有一个E是Q2组; 适用于光潜催化剂。
  • Latent acids and their use
    申请人:Yamato Hitoshi
    公开号:US20110217654A1
    公开(公告)日:2011-09-08
    The invention pertains to a compound generating an acid of the formula I or II, for instance corresponding sulfonium and iodonium salts, as well as corresponding sulfonyloximes wherein X is CH 2 or CO; Y is O, NR 4 , S, O(CO), O(CO)O, O(CO)NR 4 , OSO 2 , O(CS), or O(CS)NR 4 ; R 1 is for example C 1 -C 18 alkyl, C 1 -C 10 haloalkyl, C 2 -C 12 alkenyl, C 4 -C 30 cycloalkenyl, phenyl-C 1 -C 3 -alkyl, C 3 -C 30 cycloalkyl, C 3 -C 30 cycloalkyl-C 1 -C 18 alkyl, interrupted C 2 -C 18 alkyl, interrupted C 3 -C 30 cycloalkyl, interrupted C 3 -C 30 cycloalkyl-C 1 -C 18 alkyl, interrupted C 4 -C 30 cycloalkenyl, phenyl, naphthyl, anthracyl, phenanthryl, biphenylyl, fluorenyl or heteroaryl, all unsubstituted or are substituted; or R 1 is NR 12 R 13 ; R 2 and R 3 are for example C 3 -C 30 cycloalkylene, C 3 -C 30 cycloalkyl-C 1 -C 18 alkylene, C 1 -C 18 alkylene, C 1 -C 10 haloalkylene, C 2 -C 12 alkenylene, C 4 -C 30 cycloalkenylene, phenylene, naphthylene, anthracylene, phenanthrylene, biphenylene or heteroarylene; all unsubstituted or substituted; R 4 is for example C 3 -C 30 cycloalkyl, C 3 -C 30 cycloalkyl-C 1 -C 18 alkyl, C 1 -C 18 alkyl, C 1 -C 10 haloalkyl, C 2 -C 12 alkenyl, C 4 -C 30 cycloalkenyl, phenyl-C 1 -C 3 -alkyl; R 12 and R 13 are for example C 3 -C 30 cycloalkyl, C 3 -C 30 cycloalkyl-C 1 -C 18 alkyl, C 1 -C 18 alkyl, C 1 -C 10 haloalkyl, C 2 -C 12 alkenyl, C 4 -C 30 cycloalkenyl, phenyl-C 1 -C 3 -alkyl, Ar, (CO)R 15 , (CO)OR 15 or SO 2 R 15 ; and Ar is phenyl, biphenylyl, fluorenyl, naphthyl, anthracyl, phenanthryl or heteroaryl, all unsubstituted or substituted.
    本发明涉及一种生成公式I或II的酸的化合物,例如对应的磺鎓盐和碘鎓盐,以及对应的磺酰氧肟,其中X为CH2或CO;Y为O、NR4、S、O(CO)、O(CO)O、O(CO)NR4、OSO2、O(CS)或O(CS)NR4;R1例如为C1-C18烷基、C1-C10卤代烷基、C2-C12烯基、C4-C30环烯基、苯基-C1-C3-烷基、C3-C30环烷基、C3-C30环烷基-C1-C18烷基、中断的C2-C18烷基、中断的C3-C30环烷基、中断的C3-C30环烷基-C1-C18烷基、中断的C4-C30环烯基、苯基、萘基、蒽基、菲基、苯并二氢呋喃基或杂环基,全部未取代或被取代;或R1为NR12R13;R2和R3例如为C3-C30环烷基、C3-C30环烷基-C1-C18烷基、C1-C18烷基、C1-C10卤代烷基、C2-C12烯基、C4-C30环烯基、苯基、萘基、蒽基、菲基、苯并二氢呋喃基或杂环基,全部未取代或被取代;R4例如为C3-C30环烷基、C3-C30环烷基-C1-C18烷基、C1-C18烷基、C1-C10卤代烷基、C2-C12烯基、C4-C30环烯基、苯基-C1-C3-烷基;R12和R13例如为C3-C30环烷基、C3-C30环烷基-C1-C18烷基、C1-C18烷基、C1-C10卤代烷基、C2-C12烯基、C4-C30环烯基、苯基-C1-C3-烷基、Ar、(CO)R15、(CO)OR15或SO2R15;Ar为苯基、苯并二氢呋喃基、菲基、萘基、蒽基、苯并蒽基或杂环基,全部未取代或被取代。
  • [EN] SULPHONIUM SALT INITIATORS<br/>[FR] INITIATEURS DE SEL DE SULFONIUM
    申请人:CIBA HOLDING INC
    公开号:WO2009047105A1
    公开(公告)日:2009-04-16
    Compounds of the Formula (I), wherein L1, L'1, L'1, L2, L'2, L'2, L3, L'3, L'3, L4, L'4 and L'4 for example are hydrogen or COT; R, R' and R' for example are hydrogen,C6-C12aryl or C3-C20heteroaryl; X, X' and X' for exampleare O, S, single bond, NRa or NCORa, T is for example hydrogen, C1-C20alkyl, C3-C12cycloalkyl, C2- C20alkenyl, C5-C12cycloalkenyl, C7-C18cycloalkylenaryl, C5-C18cycloalkylenheteroaryl, C6- C14aryl, providedthat at least one of R, R' or R' is unsubstitutedor substituted C3- C20heteroaryl; and Y is an inorganic or organic anion; are suitable as photolatent acid generators.
    式(I)的化合物,其中L1,L'1,L'1,L2,L'2,L'2,L3,L'3,L'3,L4,L'4和L'4例如是氢或COT;R,R'和R'例如是氢,C6-C12芳基或C3-C20杂环芳基;X,X'和X'例如是O,S,单键,NRa或NCORa,T例如是氢,C1-C20烷基,C3-C12环烷基,C2-C20烯基,C5-C12环烯基,C7-C18环烷基芳基,C5-C18环烷基杂环芳基,C6-C14芳基,前提是至少有一个R,R'或R'是未取代或取代的C3-C20杂环芳基;而Y是无机或有机阴离子;适用于光酸发生剂。
  • Curable composition
    申请人:CIBA-GEIGY AG
    公开号:EP0462060A2
    公开(公告)日:1991-12-18
    A heat-curable composition comprising: a) an epoxide resin; and b) as curing agent, at least one aromatic amine derivative having the formula I: in which A is an n-valent aromatic residue and n is a number ranging from 2 to 400, and A is connected to a moiety CO-O- via aromatic carbon atoms. Most of the compounds of formula I are new.
    一种热固性组合物,包括:a)环氧树脂;和b)作为固化剂,至少一种具有公式I的芳香胺衍生物:其中A是n价芳香残基,n是2至400之间的数字,并且A通过芳香碳原子连接到一个CO-O-基团。公式I的大多数化合物是新的。
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(R)-4-异丙基-2-恶唑烷硫酮 麻黄恶碱 顺-八氢-2H-苯并咪唑-2-酮 顺-1-(4-氟苯基)-4-[1-(4-氟苯基)-4-羰基-1,3,8-三氮杂螺[4.5]癸-8-基]环己甲腈 非达司他 降冰片烯缩醛3-((1S,2S,4S)-双环[2.2.1]庚-5-烯-2-羰基)恶唑烷-2-酮 阿齐利特 阿那昔酮 阿洛双酮 阿帕鲁胺 阿帕他胺杂质2 铟烷-2-YL-甲基胺盐酸 钠2-{[4,5-二羟基-3-(羟基甲基)-2-氧代-1-咪唑烷基]甲氧基}乙烷磺酸酯 重氮烷基脲 詹氏催化剂 解草恶唑 解草噁唑 表告依春 螺莫司汀 螺立林 螺海因氮丙啶 螺[1-氮杂双环[2.2.2]辛烷-8,5'-咪唑烷]-2',4'-二酮 苯甲酸,4-氟-,2-[5,7-二(三氟甲基)-1,8-二氮杂萘-2-基]-2-甲基酰肼 苯氰二硫酸,1-氰基-1-甲基-4-氧代-4-(2-硫代-3-噻唑烷基)丁酯 苯妥英钠杂质8 苯妥英-D10 苯妥英 苯基硫代海因半胱氨酸钠盐 苯基硫代乙内酰脲-谷氨酸 苯基硫代乙内酰脲-蛋氨酸 苯基硫代乙内酰脲-苯丙氨酸 苯基硫代乙内酰脲-色氨酸 苯基硫代乙内酰脲-脯氨酸 苯基硫代乙内酰脲-缬氨酸 苯基硫代乙内酰脲-异亮氨酸 苯基硫代乙内酰脲-天冬氨酸 苯基硫代乙内酰脲-亮氨酸 苯基硫代乙内酰脲-丙氨酸 苯基硫代乙内酰脲-D-苏氨酸 苯基硫代乙内酰脲-(NΕ-苯基硫代氨基甲酰)-赖氨酸 苯基乙内酰脲-甘氨酸 苏氨酸-1-(苯基硫基)-2,4-咪唑烷二酮(1:1) 色氨酸标准品002 膦酸,(2-羰基-1-咪唑烷基)-,二(1-甲基乙基)酯 脱氢-1,3-二甲基尿囊素 聚(d(A-T)铯) 羟甲基-5,5-二甲基咪唑烷-2,4-二酮 羟基香豆素 美芬妥英 美芬妥英