13081-17-9 Usage
General Description
4-CHLORO-2-CYCLOHEXYLPHENOL is a chemical compound with the molecular formula C12H15ClO. It is a white crystalline solid that is used as an antiseptic and disinfectant in various pharmaceutical and personal care products. The compound has antimicrobial properties and is effective against a wide range of bacteria and fungi. It is also used in the production of agricultural and veterinary products to control the growth of microorganisms. Additionally, 4-CHLORO-2-CYCLOHEXYLPHENOL is used as a preservative in cosmetic and personal care products, as well as in industrial cleaning and preservation applications. However, it is important to handle this chemical with care, as it can be harmful if ingested or comes into contact with the skin or eyes.
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 articles and documents
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.
