41063-30-3 Usage
Description
N-(2-Hydroxypropyl)propylamine, also known as 1-(2-hydroxypropyl)propan-2-amine, is an organic compound that serves as a synthetic intermediate in the chemical industry. It is characterized by its amine functional group and hydroxyl group, which contribute to its reactivity and versatility in various chemical reactions.
Uses
N-(2-Hydroxypropyl)propylamine is used as a synthetic intermediate for various organic syntheses due to its unique chemical structure and reactivity. It can be employed in the production of various chemicals, pharmaceuticals, and other specialty products.
Used in Pharmaceutical Industry:
N-(2-Hydroxypropyl)propylamine is used as a building block for the synthesis of various pharmaceutical compounds. Its ability to form amide and ester linkages makes it a valuable component in the development of new drugs and drug candidates.
Used in Chemical Industry:
In the chemical industry, N-(2-Hydroxypropyl)propylamine is used as a versatile intermediate for the production of a wide range of chemicals, including surfactants, polymers, and specialty chemicals. Its reactivity and functional groups allow for the creation of diverse products with specific properties and applications.
Used in Cosmetics Industry:
N-(2-Hydroxypropyl)propylamine can also be found in the cosmetics industry, where it is used as a component in the formulation of personal care products. Its properties make it suitable for use in products that require emulsification, solubilization, or stabilization.
Check Digit Verification of cas no
The CAS Registry Mumber 41063-30-3 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 4,1,0,6 and 3 respectively; the second part has 2 digits, 3 and 0 respectively.
Calculate Digit Verification of CAS Registry Number 41063-30:
(7*4)+(6*1)+(5*0)+(4*6)+(3*3)+(2*3)+(1*0)=73
73 % 10 = 3
So 41063-30-3 is a valid CAS Registry Number.
41063-30-3Relevant articles and documents
Method for preparing 2-amino-4-methyl-1-propyl-1H-pyrrole-3-carbonitrile
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Paragraph 0034-0036; 0041; 0042; 0047; 0048, (2021/01/28)
The invention discloses a method for preparing 2-amino-4-methyl-1-propyl-1H-pyrrole-3-carbonitrile, and belongs to the technical field of organic synthesis. The preparation method comprises the following steps: taking epoxypropane and n-propylamine as raw materials; after hydrogen on a nitrogen atom is protected, oxidizing, removing a protecting group, and cyclizing with malononitrile to obtain the 2-amino-4-methyl-1-propyl-1H-pyrrole-3-carbonitrile. The method has the advantages of high product yield, high purity, accessible raw materials and simple operation, and is beneficial to industrialproduction.
Syntheses of five- and seven-membered ring sultam derivatives by Michael addition and Baylis-Hillman reactions
Tong, Kun,Tu, Jinchang,Qi, Xueyong,Wang, Min,Wang, Yanjie,Fu, Haizhen,Pittman Jr., Charles U.,Zhou, Aihua
supporting information, p. 2369 - 2375 (2013/03/29)
Five- and seven-membered sultam derivatives were conveniently synthesized via intra- or intermolecular Michael additions and an improved vinyl sulfonamide Baylis-Hillman reaction. Two different cyclization pathways were explored for the oxa-Michael reaction. A good solvent was discovered for an otherwise sluggish ketone-type Baylis-Hillman reaction in which vinyl sulfonamide ketones were used as the precursors. Furthermore, a strong base caused vinyl sulfonamide ketones to undergo 5-endo-trig intramolecular cyclizations, which are disfavored according to Baldwin's rule. Finally Baylis-Hillman reaction products were used as scaffolds for diversity-oriented sultam syntheses.
