7250-87-5 Usage
Uses
Used in the Oil and Gas Industry:
1,3-Dimorpholinopropan-2-ol is utilized as a corrosion inhibitor, playing a crucial role in protecting equipment and infrastructure from the damaging effects of corrosive substances, thereby extending their service life and ensuring operational efficiency.
Used in the Production of Coatings:
1,3-Dimorpholinopropan-2-ol serves as a component in the formulation of coatings, contributing to their performance characteristics such as adhesion, durability, and resistance to environmental factors. Its inclusion enhances the protective and decorative qualities of the coatings.
Used in the Production of Adhesives:
As a component in adhesive formulations, 1,3-Dimorpholinopropan-2-ol improves the bonding properties of adhesives, ensuring strong and durable adhesion between various substrates. Its presence in adhesives contributes to their overall performance and reliability.
Used in the Production of Cleaning Products:
1,3-Dimorpholinopropan-2-ol is incorporated into cleaning products to enhance their effectiveness in removing dirt, grease, and other contaminants. Its presence in these products aids in improving cleaning efficiency and promoting a cleaner and more hygienic environment.
Used as an Intermediate in the Synthesis of Pharmaceuticals:
1,3-Dimorpholinopropan-2-ol is employed as a key intermediate in the synthesis of various pharmaceuticals, contributing to the development of new and innovative medications. Its unique chemical structure allows for its use in the creation of a wide range of therapeutic agents.
Used as an Intermediate in the Synthesis of Other Organic Compounds:
Beyond its applications in the pharmaceutical industry, 1,3-Dimorpholinopropan-2-ol also serves as an intermediate in the synthesis of other organic compounds, further expanding its utility in the chemical and materials science fields. Its versatility in chemical reactions makes it a valuable component in the development of new and improved materials.
Check Digit Verification of cas no
The CAS Registry Mumber 7250-87-5 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 7,2,5 and 0 respectively; the second part has 2 digits, 8 and 7 respectively.
Calculate Digit Verification of CAS Registry Number 7250-87:
(6*7)+(5*2)+(4*5)+(3*0)+(2*8)+(1*7)=95
95 % 10 = 5
So 7250-87-5 is a valid CAS Registry Number.
InChI:InChI=1/C11H22N2O3/c14-11(9-12-1-5-15-6-2-12)10-13-3-7-16-8-4-13/h11,14H,1-10H2
7250-87-5Relevant academic research and scientific papers
Regioselective ring opening in epoxides under the action of amines in water medium
Talybov,Abbasov,Mamedbeili,Kochetkov
experimental part, p. 1819 - 1824 (2011/02/24)
Amino(bis-amino)derivatives of 2-propanol were synthesized by ring opening in epoxides under the action of amines in water medium using environmentally safe methods. The structure of the compounds obtained was established by elemental analysis and the IR, 1H and 13C NMR spectroscopy. It was found that these substances are effective bactericides. They suppress the growth of the sulfate-reducing bacteria and exhibit high anticorrosive properties.
Reactions of amines with N-hydroxy-, N-(2,3-epoxypropoxy)succinimide and naphthalimide
Ranadive, V. B.,Samant, S. D.
, p. 102 - 106 (2007/10/02)
N-Hydroxynaphthalimide (1) and N-hydroxysuccinimide (2) have been prepared. 1 is stable towards alkali, while 2 undergoes hydrolysis at room temperature in the presence of alkali. 1 reacts with amines to form only the salts while 2 reacts with an equivalent amount of primary aliphatic amine to form monoamide of succinamic acid and with an excess of a primary aliphatic amine it forms diamide of succinic acid.It reacts with an aromatic primary amine, irrespective of its concentration, to form only the mono amide of succinamic acid.N-(2,3-Epoxypropoxy)naphthalimide (9) and -succinimide (13) have been prepared from 1 and 2, respectively. 9 on reaction with amines form N-(3-amino-2-hydroxypropoxy)naphthalimides (10). 13 reacts with secondary amines to form 1,3-bisamino-2-propanol, while with aniline it forms N-(3-phenylamino-2-hydroxypropoxy)succinimide.
