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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 articles and documents

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).

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

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

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