3508-84-7 Usage
Description
1-(trichloromethyl)cyclohexan-1-ol, a chlorinated cyclohexanol with the molecular formula C7H11Cl3O, is a colorless liquid characterized by a strong, pungent odor. This chemical compound serves as a versatile intermediate in the synthesis of various pharmaceuticals, agrochemicals, and other organic compounds. Additionally, it functions as a solvent in select chemical processes. Due to its toxic nature upon ingestion or inhalation, it is crucial to handle and store 1-(trichloromethyl)cyclohexan-1-ol with appropriate safety measures to prevent exposure.
Uses
Used in Pharmaceutical Industry:
1-(trichloromethyl)cyclohexan-1-ol is utilized as a key intermediate in the production of pharmaceuticals, playing a critical role in the synthesis of various medicinal compounds. Its unique chemical structure allows for the development of drugs with specific therapeutic properties.
Used in Agrochemical Industry:
In the agrochemical sector, 1-(trichloromethyl)cyclohexan-1-ol is employed as an intermediate for the synthesis of pesticides and other agricultural chemicals. Its contribution to the development of these products helps enhance crop protection and yield.
Used in Organic Compounds Synthesis:
1-(trichloromethyl)cyclohexan-1-ol is used as an intermediate in the synthesis of a range of organic compounds, contributing to the creation of diverse chemical products with various applications across different industries.
Used as a Solvent in Chemical Processes:
1-(trichloromethyl)cyclohexan-1-ol also serves as a solvent in certain chemical processes, facilitating reactions and aiding in the production of specific chemical entities. Its solvent properties are valuable in achieving desired outcomes in chemical synthesis.
Check Digit Verification of cas no
The CAS Registry Mumber 3508-84-7 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 3,5,0 and 8 respectively; the second part has 2 digits, 8 and 4 respectively.
Calculate Digit Verification of CAS Registry Number 3508-84:
(6*3)+(5*5)+(4*0)+(3*8)+(2*8)+(1*4)=87
87 % 10 = 7
So 3508-84-7 is a valid CAS Registry Number.
InChI:InChI=1/C7H11Cl3O/c8-7(9,10)6(11)4-2-1-3-5-6/h11H,1-5H2
3508-84-7Relevant articles and documents
Pd(II)-catalyzed enantioselective C-H activation of cyclopropanes
Wasa, Masayuki,Engle, Keary M.,Lin, David W.,Yoo, Eun Jeong,Yu, Jin-Quan
supporting information; experimental part, p. 19598 - 19601 (2012/01/17)
Systematic ligand development has led to the identification of novel mono-N-protected amino acid ligands for Pd(II)-catalyzed enantioselective C-H activation of cyclopropanes. A diverse range of organoboron reagents can be used as coupling partners, and the reaction proceeds under mild conditions. These results provide a new retrosynthetic disconnection for the construction of enantioenriched cis-substituted cyclopropanecarboxylic acids.
Ring expansion/homologation-aldehyde condensation cascade using tert-trihalomethylcarbinols
Falck,He, Anyu,Manmohan Reddy,Kundu, Abhijit,Barma, Deb K.,Bandyopadhyay,Kamila, Sukanta,Akella, Radha,Bejot, Romain,Mioskowski, Charles
, p. 4645 - 4647 (2007/10/03)
Treatment of cyclic tert-trihalomethylcarbinols with CrCl2 in THF/HMPA in the presence of aryl or aliphatic aldehydes initiates a cascade sequence of one carbon ring expansion-olefination affording conjugated exocyclic ketones. Acyclic tert-trihalomethylcarbinols undergo a comparable cascade of one carbon homologation-olefination.
Direct electroreduction or use of an electrogenerated base : Two ways for the coupling of polyhalogenated compounds with aldehydes or ketones
Barhdadi, Rachid,Simsen, Blandine,Troupel, Michel,Nedelec, Jean-Yves
, p. 1721 - 1728 (2007/10/03)
The electrochemical coupling of polyhalogenated compounds with carbonyl compounds is achieved in two ways. A carbanion RX(n)- is generated either by the direct electroreduction of RX(n)Cl or by deprotonation of RX(n)H. In this latter case the base Ph- is electrogenerated by reduction of iodobenzene. All electrolysis were carried out in an undivided cell fitted with a cadmium-coated cathode and an aluminium or magnesium sacrificial anode.
