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CasNo: 26787-78-0
MF: C16H19N3O5S
Appearance: solid
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Amoxicillin is solid, while it's Molecular Formula is C16H19N3O5S. Amoxicillin is an antibiotic used in the treatment of various bacterial infections.
The CAS number of Amoxicillin is 26787-78-0.
More information of Amoxicillin 26787-78-0 are:
Synonyms |
4-Thia-1-azabicyclo[3.2.0]heptane-2-carboxylicacid, 6-[2-amino-2-(p-hydroxyphenyl)acetamido]-3,3-dimethyl-7-oxo-, D- (8CI);Eupensol;Excillin;Farconcil;Fisamox;Foxolin;Fullcilina;Gemox;Gimalxina;Gomcillin;Gramidil;Grunamox;Hiconcil;Hipen;Histocillin;Hosboral;Imacillin;Imaxilin;Imox;Imoxil;Intermox;Jerramcil;4-Thia-1-azabicyclo[3.2.0]heptane-2-carboxylic acid,6-[[amino(4-hydroxyphenyl)acetyl]amino]-3,3-dimethyl-7-oxo-, [2S-[2a,5a,6b(S*)]]-;6-[D-(-)-p-Hydroxy-a-aminobenzyl]penicillin;6-[D-a-Amino-a-(4-hydroxyphenyl)acetamido]penicillanicacid;A-Gram;Actimoxi;Agerpen;Alfamox;Almodan;Alphamox;Amagesen Solutab;Amodex;Amoflux;Amopenixin;Amoxa;Amoxal;Amoxapen;Amoxaren;Amoxi;Amoxi-Mast;Amoxicilina;Amoxidal;Amoxiden;Amoxil;Amoxin;Amoxipen;Amoxtrex;Amoxy;Amoxypen;Ampidroxyl;Ampy-Penyl;Anemol;Anemolin;Apitart;Apo-Amoxi;Ardine;Aspenil;Audumic;BLP1410;BRL 2333;Bactox;Betamox;Bimox;Biomox;Bioxidona;Bioxyllin;Cabermox;Cilamox;Clamox;Clamoxyl;Coamoxin;Comoxyl;D-(-)-a-Amino-p-hydroxybenzyl penicillin;D-2-Amino-2-(4-hydroxyphenyl)acetamidopenicillanic acid;D-Amoxicillin;Delacillin;Efpenix;Efpinex;Eupen; |
CAS Number |
26787-78-0 |
Molecular Formula |
C16H19N3O5S |
Molecular Weight |
365.41 |
Density |
1.54 g/cm3 |
Melting Point |
140 °C |
Boiling Point |
743.2 °C at 760 mmHg |
Flash Point |
403.3 °C |
HS CODE |
H19N3O5S-3H2O MOL WT. 419.45 |
PSA |
158.26000 |
LogP |
1.05280 |
Pka |
pKa 2.4 (Uncertain) |
Amoxicillin, also known as Amoxycillin, is a semi-synthetic antibiotic from the penicillin group. It is characterized by a 2-amino-2-(4-hydroxyphenyl)acetamido group at the 6 position of the penam ring. Amoxicillin is a solid substance and is known for its effectiveness in treating various bacterial infections.
InChI:InChI=1/C16H19N3O5S.3H2O/c1-16(2)11(15(23)24)19-13(22)10(14(19)25-16)18-12(21)9(17)7-3-5-8(20)6-4-7;;;/h3-6,9-11,14,20H,17H2,1-2H3,(H,18,21)(H,23,24);3*1H2/t9-,10-,11+,14-;;;/m1.../s1
Articles related to Amoxicillin:
Article |
Source |
Enzymatic synthesis of amoxicillin by the cell-bound α-amino acid ester hydrolase of Xanthomonas citri |
Kato,Kawahara,Takahashi,Igarasi , p. 821 - 825 (1980) |
Amoxicillin Inactivation by Thiol-Catalyzed Cyclization Reduces Protein Haptenation and Antibacterial Potency |
Ariza, Adriana,Blanca, Miguel,Ca?ada, F. Javier,Monta?ez, María I.,Pérez-Sala, Dolores,Pajares, María A.,Sánchez-Gómez, Francisco J.,Torres, María J.,Zimmerman, Tahl , (2020) |
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