91244-27-8 Usage
Uses
Used in Pharmaceutical Industry:
1-(2-chloroethyl)-4-isopropylbenzene is used as an intermediate for the synthesis of various pharmaceuticals. Its unique chemical structure allows it to be a key component in the development of new drugs and medications.
Used in Pesticide Industry:
In the pesticide industry, 1-(2-chloroethyl)-4-isopropylbenzene is utilized as an intermediate in the production of different types of pesticides. Its properties make it suitable for creating effective and targeted pest control solutions.
Used in Organic Compounds Synthesis:
1-(2-chloroethyl)-4-isopropylbenzene is also used as an intermediate in the synthesis of other organic compounds. Its versatility in chemical reactions contributes to the creation of a wide range of products across various industries.
Check Digit Verification of cas no
The CAS Registry Mumber 91244-27-8 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 9,1,2,4 and 4 respectively; the second part has 2 digits, 2 and 7 respectively.
Calculate Digit Verification of CAS Registry Number 91244-27:
(7*9)+(6*1)+(5*2)+(4*4)+(3*4)+(2*2)+(1*7)=118
118 % 10 = 8
So 91244-27-8 is a valid CAS Registry Number.
91244-27-8Relevant academic research and scientific papers
Polymethylhydrosiloxane reduction of carbonyl function catalysed by titanium tetrachloride
Jumbam, Ndze D.,Makaluza, Siyavuya,Masamba, Wayiza
, p. 179 - 184 (2018/04/20)
Reduction of aromatic aldehydes and ketones into the corresponding methylene derivatives by polymethylhydrosiloxane in the presence of titanium tetrachloride as catalyst was achieved in good to excellent yields ranging from 55-90%. The reaction took place under relatively mild conditions and smoothly led to the desired target molecules in the presence of other functional groups such as halogens, hydroxyl, nitro and methoxy groups. However, in the reduction of the substrate with two methoxy groups in close proximity (1,2-positions), the reaction necessitated a larger amount of the titanium catalyst and a longer reaction time to complete the reduction of the carbonyl function due to a likely complex formation of titanium tetrachloride with the methoxy groups.
