14863-58-2 Usage
Uses
Used in Agricultural Applications:
2,6-dichlorophenyl dimethylcarbamate is used as a pesticide for controlling pests on crops. It is effective in protecting agricultural produce from damage caused by insects and mites, ensuring higher yields and quality of the produce.
Used in Public Health Applications:
In the realm of public health, 2,6-dichlorophenyl dimethylcarbamate is used as an insecticide to combat vectors of disease, such as mosquitoes and ticks. Its application helps in reducing the transmission of diseases like malaria, dengue, and Lyme disease, thereby contributing to improved public health.
Used in Household and Commercial Pest Control:
2,6-dichlorophenyl dimethylcarbamate is also utilized in household and commercial settings for pest control. It is effective in eliminating insects and mites that can cause discomfort, health issues, and damage to property.
However, it is important to note that due to concerns about the potential toxicity of 2,6-dichlorophenyl dimethylcarbamate to humans and non-target organisms, it has been banned in some countries. The use of this chemical should always be carried out with caution and in accordance with the relevant regulations and safety guidelines.
Check Digit Verification of cas no
The CAS Registry Mumber 14863-58-2 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 1,4,8,6 and 3 respectively; the second part has 2 digits, 5 and 8 respectively.
Calculate Digit Verification of CAS Registry Number 14863-58:
(7*1)+(6*4)+(5*8)+(4*6)+(3*3)+(2*5)+(1*8)=122
122 % 10 = 2
So 14863-58-2 is a valid CAS Registry Number.
14863-58-2Relevant articles and documents
Room-temperature Pd-catalyzed C-H chlorination by weak coordination: One-pot synthesis of 2-chlorophenols with excellent regioselectivity
Sun, Xiuyun,Sun, Yonghui,Zhang, Chao,Rao, Yu
, p. 1262 - 1264 (2014/02/14)
A room-temperature Pd(ii)-catalyzed regioselective chlorination reaction has been developed for a facile one-pot synthesis of a broad range of 2-chlorophenols. The reaction demonstrates an excellent regioselectivity and reactivity for C-H chlorination. This reaction represents one of the rare examples of mild C-H functionalization at ambient temperature.
