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Furo(3,4:6,7)naphtho(2,3-d)-1,3-dioxol-6(8H)-one, 5,9-dihydro-5-(3,4,5-trimethoxyphenyl)-, (R)- is a complex organic compound characterized by a unique molecular structure. It features a fused ring system consisting of a furan and a naphthalene core, with a 1,3-dioxolane ring and a hydronaphthalene moiety. The compound is further defined by the presence of three methoxy groups on the phenyl ring, which is attached to the core structure. The (R)- configuration indicates the specific arrangement of the chiral center in the molecule. Furo(3,4:6,7)naphtho(2,3-d)-1,3-dioxol-6(8H)-one, 5,9-dihydro-5-(3,4,5-trimethoxyphenyl)-, (R)- is of interest in the field of organic chemistry, potentially for its pharmacological properties or as a synthetic intermediate in the preparation of more complex molecules.

477-52-1

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477-52-1 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 477-52-1 includes 6 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 3 digits, 4,7 and 7 respectively; the second part has 2 digits, 5 and 2 respectively.
Calculate Digit Verification of CAS Registry Number 477-52:
(5*4)+(4*7)+(3*7)+(2*5)+(1*2)=81
81 % 10 = 1
So 477-52-1 is a valid CAS Registry Number.

477-52-1SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 19, 2017

Revision Date: Aug 19, 2017

1.Identification

1.1 GHS Product identifier

Product name (5R)-5-(3,4,5-trimethoxyphenyl)-8,9-dihydro-5H-[2]benzofuro[5,6-f][1,3]benzodioxol-6-one

1.2 Other means of identification

Product number -
Other names Furo(3',4':6,7)naphtho(2,3-d)-1,3-dioxol-6(8H)-one,5,9-dihydro-5-(3,4,5-trimethoxyphenyl)-,(R)

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:477-52-1 SDS

477-52-1Relevant academic research and scientific papers

NOVEL DERIVATIVE OF BETA-APOPICROPODOPHYLLIN AND METHOD OF PREPARING THEREOF

-

Paragraph 0031-0033, (2021/11/13)

Provided are a novel derivative of β-apopicropodophyllin and a method of preparing the same, and more particularly, a compound represented by Formula 1 below, which is a novel derivative of β-apopicropodophyllin derived from podophyllotoxin, which is an anticancer agent, a method of preparing the same, and a composition for treating cancer, which includes the compound. In Formula 1, R is a C2 to C10 alkyl group, a C2 to C10 alkyl group containing an allyl- or alkyne, a —[CH2]n—C3 to C8 cycloalkyl group, a substituted or unsubstituted —[CH2]n-phenyl group, a substituted or unsubstituted —[CH2]n—C5 to C6 heteroaromatic group, a —C(═O)—C1 to C8 alkyl group, a substituted or unsubstituted —C(═O)—[CH2]n-phenyl group, or a substituted or unsubstituted —C(═O)—[CH2]n—C5 to C6 heteroaromatic group, wherein n is an integer of 0 to 6.

Concise synthesis of (+)-β- and γ-apopicropodophyllins, and dehydrodesoxypodophyllotoxin

Xiao, Jian,Nan, Guangming,Wang, Ya-Wen,Peng, Yu

, (2018/11/30)

Herein, we present an expeditous synthesis of bioactive aryldihydronaphthalene lignans (+)-β- and γ-apopicropodophyllins, and arylnaphthalene lignan dehydrodesoxypodophyllotoxin. The key reaction is regiocontrolled oxidations of stereodivergent aryltetralin lactones, which were easily accessed from a nickel-catalyzed reductive cascade approach developed in our group.

Total Synthesis of the Claimed Structure of (±)-Hyptinin and Structural Revision of Natural Hyptinin

Maeda, Kazuto,Hamada, Toshiyuki,Onitsuka, Satoaki,Okamura, Hiroaki

, p. 1446 - 1449 (2017/05/31)

A total synthesis of (±)-hyptinin was achieved via a convergent route using the key phosphonate, cyclic ketone, and aryl Grignard components. The 1H and 13C NMR spectra of natural hyptinin did not agree with those of the synthesized

Complete assignments of 1H and 13C NMR spectral data for 7, 7'-dihydroarylnaphthalene lignan lactones

Da Silva, Rosangela,Batista, Joao Henrique Carvalho,Da Silva Maringolo, Carine,Donate, Paulo Marcos

experimental part, p. 523 - 526 (2010/04/30)

In this article we present a complete H and C NMR spectral analysis of three 7, 7'-dihydroarylnaphthalene lignan lactones using modern NMR techniques such as COSY, HSQC, HMBC and NOE experiments. Complete assignment and homonuclear hydrogen coupling const

Asymmetric Total Synthesis of (-)-Podophyllotoxin

Andrews, Robert C.,Teague, Simon J.,Meyers, A. I.

, p. 7854 - 7858 (2007/10/02)

Using a diastereoselective addition of the appropriate aryllithium to a naphtalene-containing chiral oxazoline leads to advanced intermadiate 11 in the podophyllotoxin series.The latter is obtained in a 92:8 de.Transformation of the oxazoline moiety to the requisite lactone 18 followed by invoking the Kende route to the target gave natural (-)-podophyllotoxin in 94 percent ee.The overall yield of the sequence, accomplished in 24 steps, was 5 percent.

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