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Purpuromycin is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

53969-01-0

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53969-01-0 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 53969-01-0 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 5,3,9,6 and 9 respectively; the second part has 2 digits, 0 and 1 respectively.
Calculate Digit Verification of CAS Registry Number 53969-01:
(7*5)+(6*3)+(5*9)+(4*6)+(3*9)+(2*0)+(1*1)=150
150 % 10 = 0
So 53969-01-0 is a valid CAS Registry Number.

53969-01-0SDS

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 methyl 4,4',9',10-tetrahydroxy-7'-methoxy-5',8',9-trioxospiro[3,4-dihydropyrano[4,3-g]chromene-2,2'-3H-benzo[f][1]benzofuran]-7-carboxylate

1.2 Other means of identification

Product number -
Other names Purpuromycin

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:53969-01-0 SDS

53969-01-0Relevant academic research and scientific papers

Synthesis and antimicrobial activities of 4-purpuromycin derivatives

Trani,Dallanoce,Ferrari,Goldstein,Ripamonti,Ciabatti

, p. 503 - 512 (2007/10/03)

Purpuromycin (1) is a natural antibiotic with a broad spectrum of activity encompassing bacteria fungi and protozoa. A new series of derivatives of 1 was prepared by the modification or replacement of the C-4 hydroxyl group. The physico-chemical characteristics and the in vitro antimicrobial activity of these new semisynthetic purpuromycin derivatives are reported. Attachment of a variety of bulky groups to the C-4 hydroxyl group as well as acylation or mesylation of 1 gave derivatives with significantly reduced antifungal activity, while the antimicrobial activity of these derivatives against Gram-positive and Gram-negative bacteria was only slightly decreased. All compounds were inactive against Escherichia coli. The C-4 epimers showed different in vitro activity as compared with those having the natural configuration, particularly against fungi.

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