177545-13-0 Usage
Uses
Used in Chemical Synthesis:
5-(TRIFLUOROMETHYL)-2,3-DIHYDRO-1H-1,4-DIAZEPINE is used as a chemical intermediate for the synthesis of other compounds in the field of organic chemistry. Its unique molecular structure, featuring a trifluoromethyl group, makes it a valuable building block for creating more complex molecules with potential applications in various industries.
Used in Research and Development:
In the academic and research community, 5-(TRIFLUOROMETHYL)-2,3-DIHYDRO-1H-1,4-DIAZEPINE is employed as a subject of study to understand its chemical properties and reactivity. This knowledge can contribute to the development of new synthetic methods, reaction mechanisms, and potential applications in various fields, such as pharmaceuticals or materials science.
Used in Pharmaceutical Industry:
Although not widely commercialized, 5-(TRIFLUOROMETHYL)-2,3-DIHYDRO-1H-1,4-DIAZEPINE may be used as a precursor or component in the development of new pharmaceutical compounds. Its diazepine structure and trifluoromethyl group could potentially contribute to the creation of novel drugs with improved efficacy, selectivity, or pharmacokinetic properties.
Used in Materials Science:
5-(TRIFLUOROMETHYL)-2,3-DIHYDRO-1H-1,4-DIAZEPINE could be explored for its potential use in the development of new materials with unique properties. Its incorporation into polymers or other materials could lead to advancements in areas such as electronics, coatings, or advanced materials with tailored characteristics.
Check Digit Verification of cas no
The CAS Registry Mumber 177545-13-0 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,7,7,5,4 and 5 respectively; the second part has 2 digits, 1 and 3 respectively.
Calculate Digit Verification of CAS Registry Number 177545-13:
(8*1)+(7*7)+(6*7)+(5*5)+(4*4)+(3*5)+(2*1)+(1*3)=160
160 % 10 = 0
So 177545-13-0 is a valid CAS Registry Number.
InChI:InChI=1/C6H7F3N2/c7-6(8,9)5-1-2-10-3-4-11-5/h1-2,10H,3-4H2
177545-13-0Relevant articles and documents
One pot synthesis of 5-per(poly)fluoroalkyl-2,3-dihydro-1,4-diazepines
Wang, Quan-Fu,Mao, Yun-Yu,Hu, Chang-Ming
, p. 79 - 81 (1999)
A series of 5-per(poly)fluoroalkyl-2,3-dihydro-1,4-diazepines have been synthesized from reaction of RfCF2I with vinyl ethyl ether and ethylenediamine. A possible reaction pathway is suggested.
Fluoro organics: A facile and exclusive synthesis of novel 2- or 4-trifluoromethyl(1H,5)arylodiazepines
Chandra Sheker Reddy,Shanthan Rao,Venkataratnam
, p. 2845 - 2848 (1996)
Exclusive formation of either 2- or 4-trifluoromethyl(1H,5)arylodiazepines 4/3 was observed in the condensation of 1,1,1-trifluoro-3-(isobutoxymethylene)-2-propanones (R = H,COCF3) 2 with o-arylenediamines 1 under microwave irradiation conditio
Synthesis of 5-per(poly)fluoroalkyl-2,3-dihydro-1,4-diazepines
Wang, Quan-Fu,Hu, Bin,Luo, Bing-Hao,Hu, Chang-Ming
, p. 2377 - 2380 (1998)
A series of 5-per(poly)fluoroalkyl-2,3-dihydro-1,4-diazepines were synthesized from α-per(poly)fluoroalkyl aldehydes and ethylenediamine. A possible reaction pathway was suggested.
A novel method for preparation of trifluoromethyl substituted 2,3- dihydro-1,4-diazepine and benzimidazole
Chu, Qianli,Wang, Yanli,Zhu, Shizheng
, p. 677 - 687 (2007/10/03)
Ethylenediamine reacted readily with 4-ethoxy-1,1,1-trifluoro-3-butene- 2-one to form 5-trifluoromethyl-2,3-dihydro-1,4-diazepine in good yield. Under the same reaction conditions o-phenylene diamine gave 2-trifluoromethyl benzimidazole and benzimidazole.
