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methyl (1aS,2R,11aR)-1a-ethyl-3,8,10-trihydroxy-4,9-dioxo-1a,2,4,9,11,11a-hexahydrotetraceno[2,3-b]oxirene-2-carboxylate is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

75324-03-7

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75324-03-7 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 75324-03-7 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 7,5,3,2 and 4 respectively; the second part has 2 digits, 0 and 3 respectively.
Calculate Digit Verification of CAS Registry Number 75324-03:
(7*7)+(6*5)+(5*3)+(4*2)+(3*4)+(2*0)+(1*3)=117
117 % 10 = 7
So 75324-03-7 is a valid CAS Registry Number.

75324-03-7SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 19, 2017

Revision Date: Aug 19, 2017

1.Identification

1.1 GHS Product identifier

Product name Naphthaceno(2,3-b)oxirene-2-carboxylic acid,1a-ethyl-1a,2,4,9,11,11a-hexahydro-3,8,10-trihydroxy-4,9-dioxo-,methyl ester,(1aS-(1aalpha,2alpha,11aalpha))

1.2 Other means of identification

Product number -
Other names -

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:75324-03-7 SDS

75324-03-7Downstream Products

75324-03-7Relevant academic research and scientific papers

8-Hydroxyanthracyclinones from ε-Rhodomycinone

Lin, Horng-jau,Kumar, Virendra,Remers, William A.

, p. 1242 - 1244 (1980)

ε-Rhodomycinone was converted into 8,9-dehydro-ζ-rhodomycinone, which gave a cis diol with osmium tetroxide and a pair of epimeric epoxides with m-chloroperbenzoic acid.Acid-catalyzed opening of the epoxides gave the corresponding trans diols.In contrast, acid treatment of the trimethyl ethers of these epoxides gave predominantly a lactone and an η-rhodomycinone derivative, with only small amounts of the diols.None of the new rhodomycinones were active against Bacillus subtilis, but 8,9-dehydro-ζ-rhodomycinone was active in the induction of lytic phage in Escherichia coli.

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