1. Home
  2. S-Phenylmercapturic Acid

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)-

S-Phenylmercapturic Acid

Request for Quotation
Chemical Name: S-Phenylmercapturic Acid
CAS Number: 4775-80-8
Product Number: AG00D90U(AGN-PC-0WAFZP)
Synonyms:
MDL No:
Molecular Formula:
Molecular Weight:

Identification/Properties

Properties
MP:
110-112°C
Storage:
-10 ℃;
Form:
Solid
Computed Properties
Molecular Weight:
239.289g/mol
XLogP3:
1.4
Hydrogen Bond Donor Count:
2
Hydrogen Bond Acceptor Count:
4
Rotatable Bond Count:
5
Exact Mass:
239.062g/mol
Monoisotopic Mass:
239.062g/mol
Topological Polar Surface Area:
91.7A^2
Heavy Atom Count:
16
Formal Charge:
0
Complexity:
252
Isotope Atom Count:
0
Defined Atom Stereocenter Count:
1
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


Phenylmercapturic acid, also known as PMA, plays a crucial role in chemical synthesis as a key intermediate in the production of various compounds. This versatile acid is commonly used in the pharmaceutical industry for the synthesis of drugs and pharmaceutical intermediates. Its unique chemical properties make it a valuable building block for creating complex molecules with specific biological activities. In addition, Phenylmercapturic acid is utilized in organic chemistry laboratories for research purposes, where it serves as a precursor in the synthesis of novel compounds and materials. Its ability to undergo various chemical reactions, such as esterification or oxidation, allows for the customization of molecular structures to meet specific requirements in diverse applications. Overall, Phenylmercapturic acid is an essential reagent in chemical synthesis, enabling the development of innovative compounds with potential benefits in various industries.