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Benzylpenicillin, also known as penicillin G, is a naturally occurring antibiotic derived from the Penicillium notatum mold. It was the first penicillin to be discovered and is still widely used today. Benzylpenicillin works by inhibiting bacterial cell wall synthesis, leading to cell lysis and death. It is effective against a broad range of gram-positive bacteria, including Streptococcus, Staphylococcus, and Clostridium species. Due to its effectiveness and low toxicity, benzylpenicillin is commonly used to treat various bacterial infections such as pneumonia, meningitis, and skin infections. However, its use has been limited by the increasing prevalence of antibiotic resistance and the need for more targeted therapies.

7005-30-3

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7005-30-3 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 7005-30-3 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 7,0,0 and 5 respectively; the second part has 2 digits, 3 and 0 respectively.
Calculate Digit Verification of CAS Registry Number 7005-30:
(6*7)+(5*0)+(4*0)+(3*5)+(2*3)+(1*0)=63
63 % 10 = 3
So 7005-30-3 is a valid CAS Registry Number.

7005-30-3SDS

SAFETY DATA SHEETS

According to Globally Harmonized System of Classification and Labelling of Chemicals (GHS) - Sixth revised edition

Version: 1.0

Creation Date: Aug 15, 2017

Revision Date: Aug 15, 2017

1.Identification

1.1 GHS Product identifier

Product name 3,3-dimethyl-7-oxo-6-[(2-phenylacetyl)amino]-4-thia-1-azabicyclo[3.2.0]heptane-2-carboxylic acid

1.2 Other means of identification

Product number -
Other names Penicillin G,Benzylpenicillin

1.3 Recommended use of the chemical and restrictions on use

Identified uses For industry use only.
Uses advised against no data available

1.4 Supplier's details

1.5 Emergency phone number

Emergency phone number -
Service hours Monday to Friday, 9am-5pm (Standard time zone: UTC/GMT +8 hours).

More Details:7005-30-3 SDS

7005-30-3Upstream product

7005-30-3Relevant academic research and scientific papers

MILD PALLADIUM(0)-CATALYZED DEPROTECTION OF ALLYL ESTERS. A USEFUL APPLICATION IN THE SYNTHESIS OF CARBAPENEMS AND OTHER β-LACTAM DERIVATIVES.

Deziel, Robert

, p. 4371 - 4372 (2007/10/02)

Carbapenem and other β-lactam allyl ester derivatives are efficiently deprotected with pyrrolidine in the presence of catalytic amount of Pd(0).

6-beta-Halopenicillanic acid 1,1-dioxides as beta-lactamase inhibitors

-

, (2008/06/13)

6-beta-Halopenicillanic acid 1,1-dioxides, physiologically acceptable salts thereof and esters thereof readily hydrolyzable; pharmaceutical compositions containing a 6-beta-halopenicillanic acid 1,1-dioxide, a physiologically acceptable salt thereof or an ester thereof readily hydrolyzable; and a method for enhancing the effectiveness of a beta-lactam antibiotic, using a 6-beta-halopenicillanic acid 1,1-dioxide, a physiologically acceptable salt thereof or an ester thereof readily hydrolyzable.

ACETOXYMETHYL PENAM COMPOUNDS AS BETA-LACTAMASE INHIBITORS

-

, (2008/06/13)

2-beta-Acetoxymethyl-2-alpha-methyl-(5R)penam-3-alpha-carboxylic acid 1,1-dioxide, pharmaceutically-acceptable salts thereof and esters thereof readily hydrolyzable in vivo; pharmaceutical compositions containing 2-beta-acetoxymethyl-2-alpha-methyl-(5R)penam-3-alpha-carboxylic acid 1,1-dioxide or salt or ester thereof; and method of enhancing the effectiveness of a beta-lactam antibiotic using 2-beta-acetoxymethyl-2-alpha-methyl-(5R)penam-3-alpha-carboxylic acid 1,1-dioxide or salt or ester thereof

Method for increasing antibacterial effectiveness of a β-lactam antibiotic

-

, (2008/06/13)

6-Aminopenicillanic acid 1,1-dioxide, esters thereof readily hydrolyzable in vivo, and the pharmaceutically-acceptable salts of these compounds, are useful for enhancing the effectiveness of certain β-lactam antibiotics against certain β-lactamase producing bacteria. Derivatives of 6-aminopenicillanic acid 1,1-dioxide protected by a conventional carboxy protecting group are useful intermediates to 6-aminopenicillanic acid 1,1-dioxide and esters thereof readily hydrolyzable in vivo.

DERIVATIVES OF 6BETA-HYDROXYALKYLPENICILLANIC ACIDS AS BETA-LACTAMASE INHIBITORS

-

, (2008/06/13)

6beta-Hydroxyalkylpenicillanic acids and derivatives thereof as useful enhancers of the effectiveness of several beta-lactam antibiotics against many beta-lactamase producing bacteria, and 6beta-substituted penicillanic acid benzyl ester derivatives as useful intermediates leading to said agents which enhance the effectiveness of beta-lactam antibiotics

Penam 1,1-dioxides as beta-lactamase inhibitors

-

, (2008/06/13)

(3S, 5R)-Penam-3-carboxylic acid 1,1-dioxide, optionally having a methyl group at the 2-position, and esters thereof readily hydrolyzable in vivo, are useful for enhancing the effectiveness of several beta-lactam antibiotics against many beta-lactamase producing bacteria.

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