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2,7-Dihydroxy-5-methyl-1,4-naphthoquinone is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

41634-16-6

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41634-16-6 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 41634-16-6 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 4,1,6,3 and 4 respectively; the second part has 2 digits, 1 and 6 respectively.
Calculate Digit Verification of CAS Registry Number 41634-16:
(7*4)+(6*1)+(5*6)+(4*3)+(3*4)+(2*1)+(1*6)=96
96 % 10 = 6
So 41634-16-6 is a valid CAS Registry Number.

41634-16-6SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 13, 2017

Revision Date: Aug 13, 2017

1.Identification

1.1 GHS Product identifier

Product name 4,7-dihydroxy-5-methylnaphthalene-1,2-dione

1.2 Other means of identification

Product number -
Other names 2,7-dihydroxy-5-methyl-1,4-naphthaquinone

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:41634-16-6 SDS

41634-16-6Downstream Products

41634-16-6Relevant academic research and scientific papers

Catalyst-Controlled Transannular Polyketide Cyclization Cascades: Selective Folding of Macrocyclic Polyketides

Raps, Felix C.,F?seke, Vincent C.,H?ussinger, Daniel,Sparr, Christof

supporting information, p. 18390 - 18394 (2020/08/25)

The biomimetic synthesis of aromatic polyketides from macrocyclic substrates by means of catalyst-controlled transannular cyclization cascades is described. The macrocyclic substrates, which feature increased stability and fewer conformational states, were thereby transformed into several distinct polyketide scaffolds. The catalyst-controlled transannular cyclizations selectively led to aromatic polyketides with a defined folding and oxygenation pattern, thus emulating β-keto-processing steps of polyketide biosynthesis.

A Simple Conversion of 2-Methoxynaphthoguinones to 2,3,4,5-Tetrahydronaphthofuran-4,5-diones. Application to the Synthesis of (+/-)-Trypethelones

Guay, Vincent,Brassard, Paul

, p. 1853 - 1857 (2007/10/02)

Structures proposed for trypethelone, O-methyltrypethelone, and O-methyl-8-methoxytrypethelone have been confirmed by synthesis.The required naphthoquinone substrates were prepared regiospecifically in one step by using vinylogous ketene acetals and then converted to the desired products essentially in a novel one-flask procedure.

LAMELLICOLIC ANHYDRIDE, 4-O-CARBOMETHOXYLAMELLICOLIC ANHYDRIDE AND MONOMETHYL 3-CHLOROLAMELLICOLATE, METABOLITES OF VERTICILLIUM LAMELLICOLA

McCorkindale, N. J.,Hutchinson, S. A.,McRitchie, A. C.,Sood, G. R.

, p. 2283 - 2288 (2007/10/02)

The fungus Verticillium lamellicola affords lamellicolic anhydride 1 (5-methyl-2,4,7-trihydroxy-1,8-naphthalic anhydride) together with small amounts of the quinone 2, the carbonate 3 and the chloro compound 4.Selective reactions of the functional groups in these and their derivatives have been used to interrelate these and effect conversion of 1 into 18, the anhydride obtained from Penicillium herquei.

Synthesis of the Fungal Pigment 2,7-Dihydroxy-5-methyl-1,4-naphthoquinone

Cameron, Donald W.,Feutrill, Geoffrey I.,Griffiths, Peter G.

, p. 227 - 229 (2007/10/02)

The title compound has been synthesized and shown to be identical with material derived from the fungus Verticillium lamellicola by comparison of their respective dimethyl ethers

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