Produktname:(S)-3-(Hydroxymethyl)morpholine Hydrochloride

IUPAC Name:[(3S)-morpholin-3-yl]methanol hydrochloride

CAS:218594-79-7
Molekulare Formel:C5H12ClNO2
Reinheit:97%
Katalognummer:CM116109
Molekulargewicht:153.61

Packungseinheit Verfügbarer Vorrat Preis($) Menge
CM116109-1g in stock ǕɅ
CM116109-5g in stock ɅǕǧ
CM116109-10g in stock ƙŴȦ
CM116109-25g in stock ǕǕǕ

Nur für den Einsatz in Forschung und Entwicklung..

Anfrage-Formular

   refresh    

Produkt-Details

CAS-Nr.:218594-79-7
Molekulare Formel:C5H12ClNO2
Schmelzpunkt:-
SMILES-Code:OC[C@@H]1NCCOC1.[H]Cl
Dichte:
Katalognummer:CM116109
Molekulargewicht:153.61
Siedepunkt:
Mdl-Nr.:MFCD12547468
Lagerung:Store at 2-8°C.

Category Infos

Morpholines
Morpholine contains secondary amine groups and has all the typical reactive characteristics of secondary amine groups. It can react with inorganic acids to form salts, and react with organic acids to form salts or amides, which can be subjected to alkylation reaction, and can also be reacted with ethylene oxide, ketone or Willgerodt reaction. Morpholine is a six-membered ring containing oxygen and nitrogen, and its alkalinity is much lower than that of its parent piperidine. The marketed morpholine drugs are mainly distributed in the fields of tumors, cardiovascular and cerebrovascular diseases, respiratory system diseases, digestive system diseases, infectious diseases and mental disorders.
morpholine price
if you are interested in morpholine price, please feel free to contact us. More information of our products will be forwarded to you upon receipt of your specific inquiry.

Column Infos

Elinzanetant
On January 8, 2024, Bayer announced positive top-line results of the pivotal Phase III studies OASIS 1 and 2 evaluating the efficacy and safety of the investigational compound elinzanetant versus placebo. Elinzanetant successfully met all four primary endpoints and all three key secondary endpoints in both studies. Elinzanetant is a first dual neurokinin-1,3 (NK-1,3) receptor antagonist for the non-hormonal treatment of moderate to severe VMS associated with menopause. Elinzanetant may address moderate to severe VMS by modulating a group of estrogen sensitive neurons in the hypothalamus region of the brain (the KNDy neurons) which, with the decrease of estrogen, become hypertrophic and lead to a hyperactivation of the thermoregulatory pathway, consequently disrupting body heat control mechanisms resulting in VMS. Elinzanetant may also decrease sleep disturbances associated with menopause.