1. Home
  2. 4-Benzofurancarbonitrile

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)-

4-Benzofurancarbonitrile

N#Cc1cccc2c1cco2 Request for Quotation
Chemical Name: 4-Benzofurancarbonitrile
CAS Number: 95333-17-8
Product Number: AG003O26(AGN-PC-00LZHJ)
Synonyms:
MDL No: MFCD10699413
Molecular Formula: C9H5NO
Molecular Weight: 143.1421

Identification/Properties

Properties
BP:
260.8°C at 760 mmHg
Storage:
Room Temperature;
Form:
Solid

Safety Information

GHS Pictogram:
Signal Word:
Warning
UN#:
N/A
Hazard Statements:
H302-H315-H319-H332-H335
Precautionary Statements:
P280-P305+P351+P338-P310
Class:
N/A
Packing Group:
N/A

NMR Spectrum

Other Analytical Data

Request for Quotation

Customer Feedback

Chemical Structure


4-Benzofurancarbonitrile is a versatile building block that finds widespread applications in chemical synthesis. Its unique chemical structure allows it to serve as a valuable intermediate in the preparation of various organic compounds. This compound is commonly used in the pharmaceutical industry to synthesize complex molecules with therapeutic properties. Furthermore, it can be employed in the synthesis of agrochemicals, dyes, and materials with specialized properties. Its presence in chemical reactions often leads to the formation of diverse products with enhanced characteristics. In academic research, 4-Benzofurancarbonitrile is frequently utilized to explore new reaction pathways and develop novel synthetic strategies. Its reactivity and compatibility with different functional groups make it a valuable tool for chemists working in the field of organic synthesis.