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78854-41-8

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78854-41-8 Usage

Molecular Weight

167.16 g/mol

Structure

A bicyclic compound with a nitrogen atom in the ring system, containing a carboxylic acid and an oxo group.

Stereochemistry

(5R)-configuration, indicating the position of functional groups or substituents in relation to a chiral center.

Functional Groups

Carboxylic acid (-COOH) and oxo (=O) groups.

Potential Applications

Pharmaceutical or chemical intermediate, organic chemistry, and drug development.

Solubility

Not explicitly mentioned, but likely soluble in polar solvents like water and methanol due to the presence of a carboxylic acid group.

Stability

Not explicitly mentioned, but the presence of a carboxylic acid group suggests that it may be stable under acidic conditions.

Reactivity

May undergo reactions typical of carboxylic acids, such as esterification, amide formation, and decarboxylation.

Hazards

Not explicitly mentioned, but due to its complex structure and potential pharmaceutical applications, it should be handled with care and proper safety precautions.

Check Digit Verification of cas no

The CAS Registry Mumber 78854-41-8 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 7,8,8,5 and 4 respectively; the second part has 2 digits, 4 and 1 respectively.
Calculate Digit Verification of CAS Registry Number 78854-41:
(7*7)+(6*8)+(5*8)+(4*5)+(3*4)+(2*4)+(1*1)=178
178 % 10 = 8
So 78854-41-8 is a valid CAS Registry Number.

78854-41-8SDS

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 (5R)-7-oxo-1-azabicyclo[3.2.0]hept-2-ene-2-carboxylic acid

1.2 Other means of identification

Product number -
Other names 1-Carbapen-2-em-3-carboxylic acid

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:78854-41-8 SDS

78854-41-8Downstream Products

78854-41-8Relevant articles and documents

Mechanistic insights into the bifunctional non-heme iron oxygenase carbapenem synthase by active site saturation mutagenesis

Phelan, Ryan M.,Townsend, Craig A.

, p. 7496 - 7502 (2013/07/11)

The carbapenem class of β-lactam antibiotics is known for its remarkable potency, antibacterial spectrum, and resistance to β-lactamase-mediated inactivation. While the biosynthesis of structurally complex carbapenems, such as thienamycin, share initial biochemical steps with carbapenem-3-carboxylate ( simple carbapenem), the requisite inversion at C5 and formation of the characteristic α,β-unsaturated carboxylate are different in origin between the two groups. Here, we consider carbapenem synthase, a mechanistically distinct bifunctional non-heme iron α-ketoglutarate-dependent enzyme responsible for the terminal reactions, C5 epimerization and desaturation, in simple carbapenem production. Interestingly, this enzyme accepts two stereoisomeric substrates and transforms each to a common active antibiotic. Owing both to enzyme and product instability, resorting to saturation mutagenesis of active site and selected second-sphere residues gave clearly differing profiles of CarC tolerance to structural modification. Guided by a crystal structure and the mutational data, in silico docking was used to suggest the positioning of each disastereomeric substrate in the active site. The two orientations relative to the reactive iron-oxo center are manifest in the two distinct reactions, C5-epimerization and C2/3-desaturation. These observations favor a two-step reaction scheme involving two complete oxidative cycles as opposed to a single catalytic cycle in which an active site tyrosine, Tyr67, after hydrogen donation to achieve bicyclic ring inversion, is further hypothesized to serve as a radical carrier.

2-Substituted thio carbapenem derivatives

-

, (2008/06/13)

A process for the preparation of an antibacterially active compound of the formula (I): STR1 and salts and esters thereof wherein R1 and R2 independently are hydrogen or an organic group, and R3 is an organic group bonded

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