120800-89-7 Usage
Uses
Used in Pharmaceutical Industry:
(S)-4-benzyl-2-methylmorpholine is used as a catalyst and a reagent for [application reason] the synthesis of various pharmaceuticals. Its ability to enhance chemical reactions makes it a valuable component in the development and production of numerous medications.
Used in Agrochemical Industry:
In the agrochemical sector, (S)-4-benzyl-2-methylmorpholine is utilized as a catalyst and a reagent for [application reason] the synthesis of agrochemicals. Its role in facilitating chemical reactions is crucial for the creation of effective products in this industry.
Used as an Intermediate in Organic Synthesis:
(S)-4-benzyl-2-methylmorpholine is also used as an intermediate for [application reason] the production of other organic compounds. Its unique structure and functional groups make it a suitable candidate for use in the synthesis of a wide range of organic molecules.
Check Digit Verification of cas no
The CAS Registry Mumber 120800-89-7 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,2,0,8,0 and 0 respectively; the second part has 2 digits, 8 and 9 respectively.
Calculate Digit Verification of CAS Registry Number 120800-89:
(8*1)+(7*2)+(6*0)+(5*8)+(4*0)+(3*0)+(2*8)+(1*9)=87
87 % 10 = 7
So 120800-89-7 is a valid CAS Registry Number.
120800-89-7Relevant academic research and scientific papers
Preparation method of chiral morpholine compound
-
, (2018/10/11)
The invention provides a preparation method of a chiral morpholine compound. With chiral ethylene oxide as a raw material, the preparation method comprises the steps of ring opening, cyclization and deprotection reaction to obtain the chiral 2-substituted morpholine compound. The preparation process is simple and environmentally friendly, has mild reaction conditions, is free of irritation or allergens, has higher total yield and good safety and is suitable for industrial amplification.
Synthesis and Reaction of Optically Active Morpholinones
Kashima, Choji,Harada, Kazuo
, p. 1521 - 1526 (2007/10/02)
The reactions of variously substituted chiral morpholin-2-and-3-ones chemoselectively synthesized from chiral amino acids and lactic acid as the chiral source are described.
