431046-87-6 Usage
Derivative
Phenoxypropanoic acid 2-(4-tert-butylphenoxy)propanoyl chloride is derived from phenoxypropanoic acid, which is a class of compounds used in organic synthesis and chemical research.
Physical state
Colorless liquid It is a liquid without any color, which is a common state for many organic compounds.
Odor
Strong and irritating The compound has a pungent and bothersome smell, which may cause discomfort or health issues upon exposure.
Reactivity
Highly reactive with water and air 2-(4-tert-butylphenoxy)propanoyl chloride readily reacts with moisture and oxygen, making it sensitive to environmental conditions and requiring proper storage and handling.
Primary use
Intermediate in pharmaceutical, agrochemical, and specialty chemical production The compound serves as a building block or starting material in the synthesis of various chemicals, including pharmaceuticals, agrochemicals, and other specialty products.
Acylating agent
Potent As a potent acylating agent, 2-(4-tert-butylphenoxy)propanoyl chloride is used to modify biologically active molecules, which can lead to the development of new drugs and compounds.
Importance
Versatile chemical in organic chemistry The compound is a valuable and adaptable reagent in the field of organic chemistry, with numerous potential applications in industry and research.
Check Digit Verification of cas no
The CAS Registry Mumber 431046-87-6 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 4,3,1,0,4 and 6 respectively; the second part has 2 digits, 8 and 7 respectively.
Calculate Digit Verification of CAS Registry Number 431046-87:
(8*4)+(7*3)+(6*1)+(5*0)+(4*4)+(3*6)+(2*8)+(1*7)=116
116 % 10 = 6
So 431046-87-6 is a valid CAS Registry Number.
431046-87-6Relevant articles and documents
Highly Enantioselective Hydrogenation of Amides via Dynamic Kinetic Resolution Under Low Pressure and Room Temperature
Rasu, Loorthuraja,John, Jeremy M.,Stephenson, Elanna,Endean, Riley,Kalapugama, Suneth,Clément, Roxanne,Bergens, Steven H.
, p. 3065 - 3071 (2017/03/11)
High-throughput screening and lab-scale optimization were combined to develop the catalytic system trans-RuCl2((S,S)-skewphos)((R,R)-dpen), 2-PrONa, and 2-PrOH. This system hydrogenates functionalized α-phenoxy and related amides at room temperature under 4 atm H2 pressure to give chiral alcohols with up to 99% yield and in greater than 99% enantiomeric excess via dynamic kinetic resolution.
