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

42719-66-4

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42719-66-4 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 42719-66-4 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 4,2,7,1 and 9 respectively; the second part has 2 digits, 6 and 6 respectively.
Calculate Digit Verification of CAS Registry Number 42719-66:
(7*4)+(6*2)+(5*7)+(4*1)+(3*9)+(2*6)+(1*6)=124
124 % 10 = 4
So 42719-66-4 is a valid CAS Registry Number.
InChI:InChI=1/C14H10O6/c1-19-12-5-11-7(4-9(12)16)8-2-6(15)3-10(17)13(8)14(18)20-11/h2-5,15-17H,1H3

42719-66-4SDS

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 2,7,9-trihydroxy-3-methoxybenzo[c]chromen-6-one

1.2 Other means of identification

Product number -
Other names Altenuisol

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:42719-66-4 SDS

42719-66-4Downstream Products

42719-66-4Relevant academic research and scientific papers

Revision of the structure and total synthesis of altenuisol

Nemecek, Gregor,Cudaj, Judith,Podlech, Joachim

, p. 3863 - 3870 (2012/09/25)

A total synthesis of the reported structure of altenuisol is described. Comparison of the 1H NMR spectra of the synthesized compound and of the natural product revealed that the originally proposed structure was not correct. Consequently, two constitutional isomers were synthesized. The spectra of one of these compounds - a structure originally proposed as the structure of altertenuol - matched perfectly with the spectra of the natural product. The total synthesis of altenuisol was thus achieved starting with phloroglucinic acid and protocatechuic aldehyde in 10 steps and in 23% yield, where the longest linear sequence consisted of 6 steps. The key step was a Suzuki coupling with concomitant formation of the lactone ring. Whether altertenuol is identical with altenuisol could not be decided. Total synthesis of altenuisol, a minor toxin in ubiquitous Alternaria spp. revealed that the originally proposed structure was not correct. Altenuisol was proved to have an isomeric structure by total synthesis. Wiley-VCH Verlag GmbH & Co. KGaA, Weinheim.

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