1. Home
  2. 5-phenylmethoxy-1H-pyrrolo[2,3-c]pyridine

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)-

5-phenylmethoxy-1H-pyrrolo[2,3-c]pyridine

c1ccc(cc1)COc1ncc2c(c1)cc[nH]2 Request for Quotation
Chemical Name: 5-phenylmethoxy-1H-pyrrolo[2,3-c]pyridine
CAS Number: 17288-54-9
Product Number: AG007CB3(AGN-PC-07ZRU1)
Synonyms:
MDL No:
Molecular Formula: C14H12N2O
Molecular Weight: 224.2579

Identification/Properties

Computed Properties
Molecular Weight:
224.263g/mol
XLogP3:
2.8
Hydrogen Bond Donor Count:
1
Hydrogen Bond Acceptor Count:
2
Rotatable Bond Count:
3
Exact Mass:
224.095g/mol
Monoisotopic Mass:
224.095g/mol
Topological Polar Surface Area:
37.9A^2
Heavy Atom Count:
17
Formal Charge:
0
Complexity:
240
Isotope Atom Count:
0
Defined Atom Stereocenter Count:
0
Undefined Atom Stereocenter Count:
0
Defined Bond Stereocenter Count:
0
Undefined Bond Stereocenter Count:
0
Covalently-Bonded Unit Count:
1
Compound Is Canonicalized:
Yes

Safety Information

GHS Pictogram:
Signal Word:
Warning
UN#:
N/A
Hazard Statements:
H302-H315-H319-H335
Precautionary Statements:
P261-P305+P351+P338
Class:
N/A
Packing Group:
N/A

NMR Spectrum

Other Analytical Data

Request for Quotation

Customer Feedback

Chemical Structure


5-(Benzyloxy)-1H-pyrrolo[2,3-c]pyridine is a versatile chemical compound commonly used in chemical synthesis. Its unique structure makes it a valuable building block in the creation of various organic compounds. In chemical synthesis, this compound serves as a key intermediate in the preparation of heterocyclic compounds and pharmaceuticals. Its substituted pyrrolopyridine core provides a solid foundation for the introduction of different functional groups, enabling chemists to modify its structure according to the desired properties of the final product.Moreover, the presence of the benzyloxy group makes this compound particularly useful in cross-coupling reactions and as a protecting group in organic synthesis. By selective manipulation of the benzyloxy group, chemists can control the reactivity and selectivity of reactions, leading to efficient and precise synthesis of complex molecules.Overall, 5-(Benzyloxy)-1H-pyrrolo[2,3-c]pyridine plays a crucial role in the development of new chemical entities and the advancement of synthetic methodologies in the field of organic chemistry. Its applications extend across various research areas, making it a valuable tool for chemists seeking to create novel compounds with diverse functionalities.