- 英文名称4-Chloro-3,5-Bis(Trifluoromethyl)Benzonitrile
- 中文名称4-氯-3,5-双(三氟甲基)苯甲腈
- IUPAC名称4-chloro-3,5-bis(trifluoromethyl)benzonitrile
- 其它别名4-Chloro-3,5-Bis-Trifluoromethyl-Benzonitrile; 3,5-Bis(Trifluoromethyl)-4-Chlorobenzonitrile; 3,5-Bis(Trifluoromethyl)-4-Chlorobenzonitrile, Tech; 3,5-Bis(Trifluoromethyl)-4-Chlorobenzonitrile 93%; 3,5-Bis(Trifluoromethyl)-4-Chlorobenzonitrile; 4-Chloro-3,5-Bis(Trifluoromethyl)Benzonitrile, Technical Grade
- CAS编号62584-30-9
- MFCD编号:MFCD03412181
- EINECS号:690-457-8
- 分子式:C9H2ClF6N
- 分子量:273.56
- 产品CID: 1607294
- 产品分类有机原料→分子砌块→芳环类化合物→苯类化合物
欧盟法规
ECHA物质C&L通报海关参考信息
- 2902300000-甲苯
2903919090-氯苯
2903991000-对氯甲苯
2903399090-其他无环烃卤化衍生物 - 💡 提示:海关信息按照顺序优先匹配,如需确认的海关信息,请参考相关资料。
- 详情请参考:📖 海关编码查询和海关进出口税则
专利信息
专利号:US-9714226-B2
优先权日:2011-07-29
标题:Hydrazide containing nuclear transport modulators and uses thereof
发明人:SANDANAYAKA VINCENT P; SHACHAM SHARON; MCCAULEY DILARA; SHECHTER SHARON
权利人:KARYOPHARM THERAPEUTICS INC
摘要:The invention generally relates to nuclear transport modulators, e.g., CRM1 inhibitors, and more particularly to a compound represented by structural formula I: n nor a pharmaceutically acceptable salt thereof, wherein the values and alternative values for the variables are as defined and described herein. The invention also includes the synthesis and use of a compound of structural formula I, or a pharmaceutically acceptable salt or composition thereof, e.g., in the treatment, modulation and/or prevention of physiological conditions associated with CRM1 activity.
专利号:US-9428490-B2
优先权日:2011-07-29
标 题 :Nuclear transport modulators and uses thereof
发明人:SANDANAYAKA VINCENT P; SHACHAM SHARON; KAUFFMAN MICHAEL; SHECHTER SHARON; MCCAULEY DILARA; LANDESMAN YOSEF; SENAPEDIS WILLIAM; SAINT-MARTIN JEAN-RICHARD
权利人:SANDANAYAKA VINCENT P; SHACHAM SHARON; KAUFFMAN MICHAEL; SHECHTER SHARON; MCCAULEY DILARA; LANDESMAN YOSEF; SENAPEDIS WILLIAM; SAINT-MARTIN JEAN-RICHARD; KARYOPHARM THERAPEUTICS INC
摘要:The invention generally relates to nuclear transport modulators, e.g CRM1 inhibitors, and more particularly to a compound represented by formula (I): or a pharmaceutically acceptable salt thereof, wherein the variables are as defined and described herein. The invention also includes the synthesis and use of a compound of structural formula (I), or a pharmaceutically acceptable salt or composition thereof, e.g, in the treatment, modulation and/or prevention of physiological conditions associated with CRM1 activity.