1. Home
  2. 3-methyloxan-4-amine

Contact Angene

Tel: +852 8191 6999

Email: [email protected]

Brc1cnc(nc1)C
Pyrimidine, 5-bromo-2-methyl-
CCCP1(=O)OP(=O)(CCC)OP(=O)(O1)CCC
1,3,5,2,4,6-Trioxatriphosphorinane, 2,4,6-tripropyl-, 2,4,6-trioxide
CC1(C)OB(OC1(C)C)B1OC(C(O1)(C)C)(C)C
2,2'-Bi-1,3,2-dioxaborolane, 4,4,4',4',5,5,5',5'-octamethyl-
O=C(C=Cc1ccccc1)C=Cc1ccccc1.O=C(C=Cc1ccccc1)C=Cc1ccccc1.O=C(C=Cc1ccccc1)C=Cc1ccccc1.[Pd].[Pd]
Tris(dibenzylideneacetone)dipalladium
C1CCC(CC1)P(C1CCCCC1)C1CCCCC1.Cc1cc(C)c(c(c1)C)N1CCN(C1=[Ru](=Cc1ccccc1)(Cl)Cl)c1c(C)cc(cc1C)C
Ruthenium,[1,3-bis(2,4,6-trimethylphenyl)-2-imidazolidinylidene]dichloro(phenylmethylene)(tricyclohexylphosphine)-, (SP-5-41)-

3-methyloxan-4-amine

CC1COCCC1N Request for Quotation
Chemical Name: 3-methyloxan-4-amine
CAS Number: 1263378-30-8
Product Number: AG000SOP(AGN-PC-0352N3)
Synonyms:
MDL No:
Molecular Formula: C6H13NO
Molecular Weight: 115.1735

Identification/Properties

Safety Information

GHS Pictogram:
Signal Word:
Warning
UN#:
N/A
Hazard Statements:
H302-H315-H319-H335
Precautionary Statements:
P233-P260-P261-P264-P270-P271-P280-P301+P312-P302+P352-P304-P304+P340-P305+P351+P338-P312-P321-P330-P332+P313-P337+P313-P340-P362-P403-P403+P233-P405-P501
Class:
N/A
Packing Group:
N/A

NMR Spectrum

Other Analytical Data

Request for Quotation

Customer Feedback

Chemical Structure


3-Methyltetrahydro-2H-pyran-4-amine, also known as $name$, is a versatile compound widely utilized in chemical synthesis for its unique properties and reactivity. One key application of 3-Methyltetrahydro-2H-pyran-4-amine is in the synthesis of heterocyclic compounds. By incorporating this compound into reactions, chemists can access a diverse range of cyclic structures with potential applications in pharmaceuticals, agrochemicals, and materials science. Additionally, 3-Methyltetrahydro-2H-pyran-4-amine can serve as a valuable building block for the construction of complex molecules due to its ability to participate in various chemical transformations such as nucleophilic addition, alkylation, and cyclization reactions. By strategically harnessing the properties of this compound, chemists can efficiently create novel molecules with tailored properties and functionalities.