C14H22BN3O3
291.16 g/mol
Research ReagentWarning
4-(5-(4,4,5,5-tetramethyl-1,3,2-dioxaborolan-2-yl)pyrimidin-2-yl)morpholine
CAS957198-30-0EC894-071-2
Category
Research Reagent
Compound Class
Heterocycle
Primary Use
Research Compound
This compound is a boronic acid pinacol ester building block, commonly used in organic synthesis and pharmaceutical research. It features a morpholine-substituted pyrimidine ring with a boronate ester group, making it a versatile reagent for cross-coupling reactions.
Organic synthesis building blockPharmaceutical research reagentCross-coupling reaction substrate
Content scope: Information here supports chemical identification and industrial supply, research, and manufacturing contexts. It is not a therapeutic claim, medical advice, or drug-use instructions.
Sourcing this compound?
Post a free purchase request — no account needed. It reaches suppliers of this product, and replies go straight to your inbox.
Related Compounds
ApplicationSame Use
5-(4,4,5,5-Tetramethyl-1,3,2-dioxaborolan-2-yl)pyridin-3-ol
CAS1171891-35-2
research compound
ReferenceSame Category
3,6-Dibromopyrazine-2-amine
CAS957230-70-5
research compound
ReferenceSame Category
1-Amino(¹³C₃)imidazolidine-2,4-dione
CAS957509-31-8
research compound
ReferenceSame Category
2-NP-SCA 13C,15N2
CAS957509-32-9
research compound
ReferenceSame Category
Fmoc-4-nitro-L-phenylalanine
CAS95753-55-2
research compound
Safety Reference
Warning
H302Harmful if swallowed
H315Causes skin irritation
H319Causes serious eye irritation
H335May cause respiratory irritation
Identifiers
IUPAC Name
4-[5-(4,4,5,5-tetramethyl-1,3,2-dioxaborolan-2-yl)pyrimidin-2-yl]morpholine
InChIKey
HNVAYPJNFUXYII-UHFFFAOYSA-N
SMILES
B1(OC(C(O1)(C)C)(C)C)C2=CN=C(N=C2)N3CCOCC3
Synonyms (8)
—
Sourcing this compound?
Post a free purchase request — no account needed. It reaches suppliers of this product, and replies go straight to your inbox.