Product Name:Methyl 7-oxa-2-azabicyclo[4.1.0]heptane-2-carboxylate

IUPAC Name:methyl 7-oxa-2-azabicyclo[4.1.0]heptane-2-carboxylate

CAS:286-25-9
Molecular Formula:C7H11NO3
Purity:95%+
Catalog Number:CM539011
Molecular Weight:157.17

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CM539011-1g 1-2 Weeks ŁţǎƏ

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Product Details

CAS NO:286-25-9
Molecular Formula:C7H11NO3
Melting Point:-
Smiles Code:O=C(N1CCCC2C1O2)OC
Density:
Catalog Number:CM539011
Molecular Weight:157.17
Boiling Point:
MDL No:
Storage:

Category Infos

Piperidines
Piperidine is an azacycloalkane that is cyclohexane in which one of the carbons is replaced by a nitrogen. Although piperidine is a common organic compound, it is an immensely important class of compounds medicinally: the piperidine ring is the most common heterocyclic subunit among FDA approved drugs.
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Bridged Compounds
Bridged ring compound refers to any two rings in the compound, which share two non-directly connected carbon atoms, and are classified into bicyclic hydrocarbons, tricyclic hydrocarbons, tetracyclic hydrocarbons, etc. Carbon atoms used in two or more rings are bridgehead carbon atoms, and the bond connecting the bridgehead carbon atoms is called a bridge. Bridged ring compounds are a class of organic compounds that are widely present in nature and usually have important physiological activities, such as the famous anticancer drug paclitaxel and antimalarial drug artemisinin.
bridged compounds,bridged bicyclic compounds
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Oxiranes
Oxirane is a three-membered ring compound consisting of one oxygen atom and two carbon atoms. Oxirane is present in natural products such as cryptocin, which has anticancer properties, and azidomycin, trienone, and epoxidomycin, which have shown activity against drug-resistant leukemias and AIDS-related lymphomas. Other oxirane containing bioactive molecules have anti-inflammatory, immunosuppressive, and antitumor activities. Oxiranes are a strained ring susceptible to various nucleophilic, ring-opening or rearrangement reactions, so they are considered to be one of the most important intermediates in organic synthesis.