13081-17-9 Usage
Uses
Used in Pharmaceutical and Personal Care Products:
4-CHLORO-2-CYCLOHEXYLPHENOL is used as an antiseptic and disinfectant for its ability to combat microorganisms, ensuring the safety and efficacy of pharmaceutical products and personal care items.
Used in Agricultural and Veterinary Products:
In this industry, 4-CHLORO-2-CYCLOHEXYLPHENOL is used as a microbiological control agent to manage the growth of unwanted microorganisms, thereby preserving the quality and safety of agricultural and veterinary products.
Used in Cosmetic Preservation:
4-CHLORO-2-CYCLOHEXYLPHENOL is utilized as a preservative in cosmetic products to prevent the proliferation of bacteria and fungi, thereby extending the shelf life and maintaining the integrity of these products.
Used in Industrial Cleaning and Preservation:
4-CHLORO-2-CYCLOHEXYLPHENOL is also employed in industrial settings as a cleaning and preservation agent, leveraging its antimicrobial properties to keep surfaces and equipment free from microbial contamination.
It is crucial to handle 4-CHLORO-2-CYCLOHEXYLPHENOL with care due to its potential harmful effects if ingested or upon contact with skin or eyes, emphasizing the need for proper safety measures during its use.
Check Digit Verification of cas no
The CAS Registry Mumber 13081-17-9 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 1,3,0,8 and 1 respectively; the second part has 2 digits, 1 and 7 respectively.
Calculate Digit Verification of CAS Registry Number 13081-17:
(7*1)+(6*3)+(5*0)+(4*8)+(3*1)+(2*1)+(1*7)=69
69 % 10 = 9
So 13081-17-9 is a valid CAS Registry Number.
InChI:InChI=1/C12H15ClO/c13-10-6-7-12(14)11(8-10)9-4-2-1-3-5-9/h6-9,14H,1-5H2
13081-17-9Relevant academic research and scientific papers
Iodoarene-Catalyzed Stereospecific Intramolecular sp3 C-H Amination: Reaction Development and Mechanistic Insights
Zhu, Chendan,Liang, Yong,Hong, Xin,Sun, Heqing,Sun, Wei-Yin,Houk,Shi, Zhuangzhi
supporting information, p. 7564 - 7567 (2015/06/30)
A new strategy is reported for intramolecular sp3 C-H amination under mild reaction conditions using iodoarene as catalyst and m-CPBA as oxidant. This C-H functionalization involving iodine(III) reagents generated in situ occurs readily at sterically hindered tertiary C-H bonds. DFT (M06-2X) calculations show that the preferred pathway involves an iodonium cation intermediate and proceeds via an energetically concerted transition state, through hydride transfer followed by the spontaneous C-N bond formation. This leads to the experimentally observed amination at a chiral center without loss of stereochemical information.
