60162-33-6 Usage
Uses
Used in Pharmaceutical and Agrochemical Industries:
METHYL P-METHYL-ALPHA-CHLORO PHENYLACETATE is used as a key intermediate in the synthesis of various pharmaceuticals and agrochemicals, contributing to the development of new drugs and pesticides.
Used in Perfumery and Flavoring Industry:
It is utilized as a building block in the creation of perfumes and flavorings, enhancing the aromatic profiles of these products and providing unique scents and tastes.
Used as an Artificial Fruit Flavoring Agent:
METHYL P-METHYL-ALPHA-CHLORO PHENYLACETATE is employed to mimic natural fruit flavors, offering a consistent and controlled flavor profile in food and beverage applications.
Used in Organic Synthesis as a Reagent:
It serves as a reagent in organic synthesis, facilitating various chemical reactions and contributing to the production of a wide range of organic compounds.
Used as a Solvent in Industrial Processes:
METHYL P-METHYL-ALPHA-CHLORO PHENYLACETATE is used as a solvent in various industrial processes, aiding in the dissolution and reaction of substances in manufacturing operations.
Check Digit Verification of cas no
The CAS Registry Mumber 60162-33-6 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 6,0,1,6 and 2 respectively; the second part has 2 digits, 3 and 3 respectively.
Calculate Digit Verification of CAS Registry Number 60162-33:
(7*6)+(6*0)+(5*1)+(4*6)+(3*2)+(2*3)+(1*3)=86
86 % 10 = 6
So 60162-33-6 is a valid CAS Registry Number.
InChI:InChI=1/C10H11ClO2/c1-7-3-5-8(6-4-7)9(11)10(12)13-2/h3-6,9H,1-2H3
60162-33-6Relevant academic research and scientific papers
Enantioselective α-Chlorination Reactions of in Situ Generated C1 Ammonium Enolates under Base-Free Conditions
Stockhammer, Lotte,Weinzierl, David,B?gl, Thomas,Waser, Mario
, p. 6143 - 6147 (2021/08/18)
The asymmetric α-chlorination of activated aryl acetic acid esters can be carried out with high levels of enantioselectivities utilizing commercially available isothiourea catalysts under base-free conditions. The reaction, which proceeds via the in situ formation of chiral C1 ammonium enolates, is best carried out under cryogenic conditions combined with a direct trapping of the activated α-chlorinated ester derivative to prevent epimerization, thus allowing for enantioselectivities of up to e.r. 99:1.
Polymorphs of bicifadine hydrochloride
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Page 4, (2008/06/13)
A new polymorphic crystalline form of bicifadine hydrochloride, designated form B, which is more thermodynamically stable than the previously known polymorphic form of bicifadine hydrochloride, designated as form A, methods for preparing said crystalline
