1005-04-5 Usage
Uses
Used in Pharmaceutical Industry:
(2-morpholin-4-ylpropyl)amine(SALTDATA: FREE) is used as a pharmaceutical intermediate for the synthesis of amine-based drugs. It plays a critical role in the production of medications such as antihistamines, which are used to treat allergic reactions, antitussives for suppressing cough, and antihypertensives to manage high blood pressure.
Used in Chemical Industry:
In the chemical industry, (2-morpholin-4-ylpropyl)amine(SALTDATA: FREE) is used as a building block in the synthesis of various organic compounds. Its applications extend to the creation of polymers, which are large molecules composed of repeating structural units, and surfactants, which are compounds that lower the surface tension of a liquid, making it useful in a wide range of products from detergents to paints.
As a salt in its free form, (2-morpholin-4-ylpropyl)amine(SALTDATA: FREE) offers flexibility in its applications across different sectors, making it a valuable component in the development and manufacturing of diverse products in the pharmaceutical and chemical industries.
Check Digit Verification of cas no
The CAS Registry Mumber 1005-04-5 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 1,0,0 and 5 respectively; the second part has 2 digits, 0 and 4 respectively.
Calculate Digit Verification of CAS Registry Number 1005-04:
(6*1)+(5*0)+(4*0)+(3*5)+(2*0)+(1*4)=25
25 % 10 = 5
So 1005-04-5 is a valid CAS Registry Number.
1005-04-5Relevant academic research and scientific papers
NEW RENIN-INHIBITORY OLIGOPEPTIDES, THEIR PREPARATION AND THEIR USE
-
, (2008/06/13)
Oligopeptides of formula (I): STR1 where R 1-R 5 are various organic groups, and A represents a group of formula--NH--or--(CH 2) n--, in which n represents an integer of from 1 to 3, have renin-inhibitory activity and are particularly suitable for oral administration. They may be prepared by condensing their component amino acids or lower oligopeptides using conventional peptide synthesis reactions.
DIRECT NUCLEOPHILIC SUBSTITUTION IN 2-HALOALKYLAMINES: NEW ROUTE TO SUBSTITUTED ETHYLENEDIAMINES
Chechik, V. O.,Bobylev, V. A.
, p. 1501 - 1502 (2007/10/03)
Nucleophilic substitution in 2-haloalkylamines in weakly polar media was found to proceed partially without intermediate formation of aziridines.This makes it possible to obtain pure substituted ethylenediamines.
