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(2R,3E,5R)-3-(2-hydroxyethylidene)-7-oxo-4-oxa-1-azabicyclo[3.2.0]heptane-2-carboxylic acid is a complex organic compound with a unique molecular structure. It is characterized by a bicyclic ring system, with one ring being a three-membered aziridine ring and the other a seven-membered cycloheptane ring. The molecule contains several functional groups, including a carboxylic acid group, a hydroxyl group, and a double bond. The stereochemistry of the molecule is defined by the R configuration at the 2nd, 3rd, and 5th carbon atoms, with the 3rd carbon also featuring a trans (E) double bond. (2R,3E,5R)-3-(2-hydroxyethylidene)-7-oxo-4-oxa-1-azabicyclo[3.2.0]heptane-2-carboxylic acid is of interest in the field of organic chemistry and may have potential applications in pharmaceuticals or other industries, although its specific uses are not detailed in the provided information.

62319-53-3

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62319-53-3 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 62319-53-3 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 6,2,3,1 and 9 respectively; the second part has 2 digits, 5 and 3 respectively.
Calculate Digit Verification of CAS Registry Number 62319-53:
(7*6)+(6*2)+(5*3)+(4*1)+(3*9)+(2*5)+(1*3)=113
113 % 10 = 3
So 62319-53-3 is a valid CAS Registry Number.

62319-53-3SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 20, 2017

Revision Date: Aug 20, 2017

1.Identification

1.1 GHS Product identifier

Product name (2R,5R)-3-(2-hydroxyethylidene)-7-oxo-4-oxa-1-azabicyclo[3.2.0]heptane-2-carboxylic acid

1.2 Other means of identification

Product number -
Other names Acide clavulanique

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:62319-53-3 SDS

62319-53-3Upstream product

62319-53-3Downstream Products

62319-53-3Relevant academic research and scientific papers

The Roles of Clavaminic Acid and Proclavaminic Acid in Clavunalic Acid Biosynthesis

Elson, Stephen W.,Baggaley, Keith H.,Gillett, Janet,Holland, Susan,Nicholson, Neville H.,et al.

, p. 1739 - 1740 (1987)

Clavunalic acid samples isolated from fermentations of Streptomyces clavuligerus ATCC 27064 fed with 13C-clavaminic acid or 13C-proclavaminic acid were found to be appropriately labelled, indicating that the title compounds are biosynthetic precursors of clavunalic acid.

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