1. Home
  2. 1H-Indole-3-carboxaldehyde, 2-phenyl-

Contact Angene

Tel: +852 8191 6999

Email: sales@angenechemical.com

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)-

1H-Indole-3-carboxaldehyde, 2-phenyl-

N1CC2(C1)COC2.OC(=O)C(=O)O Request for Quotation
Chemical Name: 1H-Indole-3-carboxaldehyde, 2-phenyl-
CAS Number: 1159599-99-1
Product Number: AG000H7I(AGN-PC-0JTSWO)
Synonyms:
MDL No:
Molecular Formula: C7H11NO5
Molecular Weight: 189.1659

Identification/Properties

Computed Properties
Molecular Weight:
189.167g/mol
Hydrogen Bond Donor Count:
3
Hydrogen Bond Acceptor Count:
6
Rotatable Bond Count:
1
Exact Mass:
189.064g/mol
Monoisotopic Mass:
189.064g/mol
Topological Polar Surface Area:
95.9A^2
Heavy Atom Count:
13
Formal Charge:
0
Complexity:
154
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:
2
Compound Is Canonicalized:
Yes

Safety Information

NMR Spectrum

Other Analytical Data

Request for Quotation

Customer Feedback

Chemical Structure


2-Oxa-6-azaspiro[3.3]heptane oxalate, a versatile compound used in chemical synthesis, serves as a crucial building block in the creation of various organic molecules. This unique substance plays a pivotal role in the development of synthetic routes for the synthesis of complex compounds with diverse applications. By incorporating 2-Oxa-6-azaspiro[3.3]heptane oxalate into chemical reactions, researchers can access novel structural motifs and facilitate the formation of intricate molecular frameworks. Its strategic use in synthetic chemistry enables the efficient construction of biologically active compounds, pharmaceutical intermediates, and advanced materials. This compound acts as a key precursor in the synthesis of specialized molecules, showcasing its significance in the realm of organic chemistry.