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BACAMPICILLIN HYDROCHLORIDE
  • Chemical Name: BACAMPICILLIN HYDROCHLORIDE
  • CAS No.: 37661-08-8

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What is the BACAMPICILLIN HYDROCHLORIDE ?

BACAMPICILLIN HYDROCHLORIDE is , while it's Molecular Formula is C21H27 N3 O7 S . Cl H. Bacampicillin is a penicillin class of antibiotic. Bacampicillin is a prodrug of ampicillin (A634300) with improved oral bioavailability.

What is the CAS number for BACAMPICILLIN HYDROCHLORIDE ?

The CAS number of BACAMPICILLIN HYDROCHLORIDE is 37661-08-8.

More information of BACAMPICILLIN HYDROCHLORIDE 37661-08-8 are:

Synonyms

4-Thia-1-azabicyclo[3.2.0]heptane-2-carboxylicacid, 6-[(aminophenylacetyl)amino]-3,3-dimethyl-7-oxo-,1-[(ethoxycarbonyl)oxy]ethyl ester, monohydrochloride, [2S-[2a,5a,6b(S*)]]-; 4-Thia-1-azabicyclo[3.2.0]heptane-2-carboxylic acid,6-[[(2R)-aminophenylacetyl]amino]-3,3-dimethyl-7-oxo-,1-[(ethoxycarbonyl)oxy]ethyl ester, monohydrochloride, (2S,5R,6R)- (9CI);Ambacamp; Ambaxin; Bacacil; Bacampicillin-hydrochloride; Bacampicine;Becampicillin hydrochloride; Penglobe; Spectrobid

CAS?Number

37661-08-8

Molecular Formula

C21H27 N3 O7 S . Cl H

Molecular Weight

501.988

Melting Point

171-176° (dec)

Boiling Point

695.4°C at 760 mmHg

Flash Point

374.3°C

PSA

162.56000

LogP

3.12690

What is BACAMPICILLIN HYDROCHLORIDE (37661-08-8) used for?

Bacampicillin Hydrochloride is a semi-synthetic antibiotic belonging to the penicillin class. It is a prodrug of ampicillin, which means it is converted into ampicillin after administration, providing improved oral bioavailability. This allows for effective treatment of various bacterial infections when taken orally.

InChI:InChI=1/C21H27N3O7S.ClH/c1-5-29-20(28)31-11(2)30-19(27)15-21(3,4)32-18-14(17(26)24(15)18)23-16(25)13(22)12-9-7-6-8-10-12;/h6-11,13-15,18H,5,22H2,1-4H3,(H,23,25);1H/t11?,13-,14?,15?,18?;/m1./s1

Articles related to BACAMPICILLIN HYDROCHLORIDE:

Article

Source

Preparation of 1'-ethoxycarbonyl-oxyethyl esters of penicillins

-

, (2008/06/13)

Studies on prodrugs. III. A convenient and practical preparation of ampicillin prodrugs

Ikeda,Sakamoto,Kondo,et al.

, p. 4316 - 4322 (2007/10/02)

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