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4-(1,3-Benzodioxol-5-yl)-5,6,7-trimethoxynaphtho[2,3-c]furan-1(3H)-one is a complex organic compound characterized by a naphtho[2,3-c]furan-1(3H)-one core structure, which features a naphthalene ring fused to a furan ring. The molecule is adorned with a 1,3-benzodioxole group at the 4-position, which contributes to its aromatic character, and three methoxy groups at the 5, 6, and 7 positions, enhancing its solubility and potentially affecting its reactivity. This chemical is known for its unique structure and properties, which may have implications in various fields such as pharmaceuticals, materials science, or as a synthetic intermediate in organic chemistry. Its specific applications and properties would depend on further research and characterization.

6258-43-1

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6258-43-1 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 6258-43-1 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 6,2,5 and 8 respectively; the second part has 2 digits, 4 and 3 respectively.
Calculate Digit Verification of CAS Registry Number 6258-43:
(6*6)+(5*2)+(4*5)+(3*8)+(2*4)+(1*3)=101
101 % 10 = 1
So 6258-43-1 is a valid CAS Registry Number.

6258-43-1SDS

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 4-(1,3-benzodioxol-5-yl)-5,6,7-trimethoxy-3H-benzo[f][2]benzofuran-1-one

1.2 Other means of identification

Product number -
Other names chaihunaphthone

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:6258-43-1 SDS

6258-43-1Downstream Products

6258-43-1Relevant academic research and scientific papers

A Garratt-Braverman route to aryl naphthalene lignans

Mondal, Sayantan,Maji, Manasi,Basak, Amit

experimental part, p. 1183 - 1186 (2011/03/21)

A series of aryl naphthalene lignans were prepared in good yields starting from substituted bis-propargyl ethers. The method involved a base-mediated Garratt-Braverman cyclization followed by benzylic oxidation to the lactone. The chemoselectivity in the

Synthesis and biological activity of bromolignans and cyclolignans

San Feliciano,Medarde,Pelaez Lamamie De Clairac,Lopez,Puebla,Gravalos,Lazaro,De Quesada

, p. 421 - 426 (2007/10/02)

Nine lignan derivatives (4-12) have been obtained from (-)-yatein by treatment with DDQ and NBS. They showed moderate antineoplastic activity (P-388, A-549, HT-29) compared with podophyllotoxin, but some of them have a better therapeutic index. None of the tested compounds shows antiviral (HSV-1, VSV) or enzyme inhibitor (ADA, DHFR, GST) activities.

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