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(4-Methoxyphenyl)methyl (2S,5R,6R)-3,3-dimethyl-4,7-dioxo-6-[(2-phenylacetyl)amino]-4lambda4-thia-1-azabicyclo[3.2.0]heptane-2-carboxylate is a complex organic molecule with a molecular formula of C30H31NO6S. It features a 4-methoxyphenylmethyl group attached to a bicyclic amino acid backbone, which includes a 3,3-dimethyl-4,7-dioxo-6-[(2-phenylacetyl)amino]-4lambda4-thia-1-azabicyclo[3.2.0]heptane-2-carboxylate moiety. This ester derivative is characterized by its unique stereochemistry and the presence of a phenylacetyl group, indicating potential pharmaceutical applications, such as serving as a drug or pharmaceutical intermediate. Further experimental investigation is required to elucidate its specific biological and pharmacological properties.

53956-74-4

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53956-74-4 Usage

Uses

Used in Pharmaceutical Industry:
(4-Methoxyphenyl)methyl (2S,5R,6R)-3,3-dimethyl-4,7-dioxo-6-[(2-phenylacetyl)amino]-4lambda4-thia-1-azabicyclo[3.2.0]heptane-2-carboxylate is used as a potential drug or pharmaceutical intermediate for its unique structural features and the possibility of exhibiting specific biological activities. (4-Methoxyphenyl)methyl (2S,5R,6R)-3,3-dimethyl-4,7-dioxo-6-[(2-phenylacetyl)amino]-4lambda4-thia-1-azabicyclo[3.2.0]heptane-2-carboxylate's ester nature and the presence of a phenylacetyl group may contribute to its potential therapeutic effects, which need to be experimentally determined for various medical applications.

Check Digit Verification of cas no

The CAS Registry Mumber 53956-74-4 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 5,3,9,5 and 6 respectively; the second part has 2 digits, 7 and 4 respectively.
Calculate Digit Verification of CAS Registry Number 53956-74:
(7*5)+(6*3)+(5*9)+(4*5)+(3*6)+(2*7)+(1*4)=154
154 % 10 = 4
So 53956-74-4 is a valid CAS Registry Number.

53956-74-4SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 16, 2017

Revision Date: Aug 16, 2017

1.Identification

1.1 GHS Product identifier

Product name p-methoxybenzyl 6-phenacetamidopenicillanate-1-oxide

1.2 Other means of identification

Product number -
Other names GEO

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:53956-74-4 SDS

53956-74-4Relevant academic research and scientific papers

Preparation of 7-phenylacetamide-3-chloromethyl-cephalosporanic acid p-methoxybenzyl ester

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Paragraph 0024; 0025, (2017/09/02)

The invention belongs to the field of synthesis of cephalosporin drug intermediates and disclosesa preparation method of 7-phenylacetamide-3-chloromethyl-cephalosporanic acid p-methoxybenzyl ester (short for GCLE). According to the method, penicillin G potassium salt taken as an initial raw material reacts with 4-methoxybenzylchloride firstly, penicillin sulfoxide ester is prepared through oxidation with peracetic acid and reacts with 2-mercaptobenzothiazole firstly, then a product reacts with benzene sulfinic acid, a ring opening product is obtained and reacts with chlorine, sodium methoxide is used for ring closing under the action of a methanol solvent, and 7-phenylacetamide-3-chloromethyl-cephalosporanic acid p-methoxybenzyl ester is obtained. The solvent is simple and easy to recover, reaction conditions are mild, operation is simple and convenient, and industrial production is easy.

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