1. Home
  2. 2-[(2-fluorophenyl)sulfonylamino]acetic acid

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)-

2-[(2-fluorophenyl)sulfonylamino]acetic acid

OC(=O)CNS(=O)(=O)c1ccccc1F Request for Quotation
Chemical Name: 2-[(2-fluorophenyl)sulfonylamino]acetic acid
CAS Number: 554438-95-8
Product Number: AG00DBBY(AGN-PC-0JV3CH)
Synonyms:
MDL No: MFCD03618982
Molecular Formula: C8H8FNO4S
Molecular Weight: 233.2168

Identification/Properties

Computed Properties
Molecular Weight:
233.213g/mol
XLogP3:
0.6
Hydrogen Bond Donor Count:
2
Hydrogen Bond Acceptor Count:
6
Rotatable Bond Count:
4
Exact Mass:
233.016g/mol
Monoisotopic Mass:
233.016g/mol
Topological Polar Surface Area:
91.8A^2
Heavy Atom Count:
15
Formal Charge:
0
Complexity:
324
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

NMR Spectrum

Other Analytical Data

Request for Quotation

Customer Feedback

Chemical Structure


The compound N-[(2-Fluorophenyl)sulfonyl]glycine plays a crucial role in chemical synthesis as a versatile building block. Its unique structure containing a sulfonyl group and a glycine moiety enables it to participate in various synthetic reactions. This compound can be utilized as a key intermediate in the creation of pharmaceuticals, agrochemicals, and other fine chemicals. In organic synthesis, N-[(2-Fluorophenyl)sulfonyl]glycine is commonly employed for introducing the sulfonyl functionality into target molecules, facilitating further derivatization and modification. Its compatibility with a range of reaction conditions and its ability to selectively react with specific functional groups make it a valuable tool for chemists striving to develop new compounds with tailored properties.