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3',4'-DIMETHOXY-BIPHENYL-2-CARBALDEHYDE, also known as 2,2'-Dihydroxy-3,3',4,4'-tetramethoxy-5,5'-bibenzyloxydiphenylmethane, is a chemical compound with the molecular formula C18H18O5. It is a derivative of biphenyl and has two methoxy groups attached to the phenyl rings. 3',4'-DIMETHOXY-BIPHENYL-2-CARBALDEHYDE is known for its versatile applications in various fields due to its unique chemical structure.

676348-35-9

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676348-35-9 Usage

Uses

Used in Organic Synthesis:
3',4'-DIMETHOXY-BIPHENYL-2-CARBALDEHYDE is used as a key intermediate in organic synthesis for the production of various chemical compounds. Its unique structure allows for the creation of a wide range of molecules, making it a valuable building block in the synthesis process.
Used in Pharmaceutical Industry:
In the pharmaceutical industry, 3',4'-DIMETHOXY-BIPHENYL-2-CARBALDEHYDE is used as a starting material for the development of new drugs. Its potential biological activities and pharmacological properties make it a promising candidate for the treatment of various diseases and conditions.
Used in Agrochemical Industry:
3',4'-DIMETHOXY-BIPHENYL-2-CARBALDEHYDE also finds application in the agrochemical industry, where it serves as a precursor for the synthesis of various agrochemicals. Its use in this industry contributes to the development of effective solutions for agricultural challenges.
Used in Electronic Materials Development:
3',4'-DIMETHOXY-BIPHENYL-2-CARBALDEHYDE has been investigated for its potential use in the development of electronic materials. Its unique properties make it a candidate for use in the creation of advanced materials for electronic devices and components.
Used as a Precursor for Polymer and Resin Synthesis:
Furthermore, 3',4'-DIMETHOXY-BIPHENYL-2-CARBALDEHYDE is utilized as a precursor in the synthesis of polymers and resins. Its role in this process is crucial for the development of new materials with specific properties for various applications.

Check Digit Verification of cas no

The CAS Registry Mumber 676348-35-9 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 6,7,6,3,4 and 8 respectively; the second part has 2 digits, 3 and 5 respectively.
Calculate Digit Verification of CAS Registry Number 676348-35:
(8*6)+(7*7)+(6*6)+(5*3)+(4*4)+(3*8)+(2*3)+(1*5)=199
199 % 10 = 9
So 676348-35-9 is a valid CAS Registry Number.

676348-35-9SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 18, 2017

Revision Date: Aug 18, 2017

1.Identification

1.1 GHS Product identifier

Product name 2-(3,4-dimethoxyphenyl)benzaldehyde

1.2 Other means of identification

Product number -
Other names 3',4'-dimethoxybiphenyl-2-carbaldehyde

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:676348-35-9 SDS

676348-35-9Relevant articles and documents

K2S2O8-promoted radical trifluoromethylthiolation/spirocyclization for the synthesis of SCF3?featured spiro[5,5]trienones

Dai, Peng,Li, Bing,Shen, Liu-Yu,Sun, Yu,Wang, Yu-Qi,Yang, Wen-Chao

supporting information, (2022/01/24)

A direct and efficient strategy for the trifluoromethylthiolation and dearomatization of biaryl ynones with stable and readily available AgSCF3 has been developed. The reaction occurs smoothly in the presence of K2S2O8 via a 6-exo-trig radical cyclization, providing a variety of SCF3-containing spiro [5,5]trienones in good yields.

Novel Biphenyl Derivative Compound and Use Thereof

-

Paragraph 0065-0067, (2021/07/17)

The present disclosure provides a novel biphenyl derivative compound or a pharmaceutically acceptable salt thereof. The biphenyl derivative compound or pharmaceutically acceptable salt thereof according to the present disclosure is a compound that increas

Electrochemical Trifluoromethylthiolation and Spirocyclization of Alkynes with AgSCF3: Access to SCF3-Containing Spiro[5,5]trienones

Yang, Wen-Chao,Zhang, Ming-Ming,Sun, Yu,Chen, Cai-Yun,Wang, Lei

supporting information, p. 6691 - 6696 (2021/09/08)

A novel and efficient strategy for trifluoromethylthiolation and dearomatization of activated alkynes with stable and readily available AgSCF3 has been developed. Reported herein is the unprecedented electrochemical generation of the SCF3 radical in the absence of persulfate for the synthesis of SCF3-containing spiro[5,5]trienones in good yields via a 6-exo-trig radical cyclization.

PHARMACEUTICAL COMPOSITION, CONTAINING NM23 ACTIVATOR, FOR INHIBITING CANCER METASTASIS

-

Paragraph 0048-0049, (2020/03/17)

The present disclosure relates to a pharmaceutical composition for suppressing cancer metastasis containing, as an active ingredient, an activator compound of the cancer metastasis inhibitor Nm23, a stereoisomer thereof, or a pharmaceutically acceptable s

Atom-economic threefold cross-couplings of triarylbismuth reagents with 2-halobenzaldehydes and pot-economic in situ Wittig functionalizations with phosphonium salts

Rao, Maddali L. N.,Dhanorkar, Ritesh J.

, p. 63792 - 63806 (2015/02/19)

In this paper we report an efficient pot-economic methodology for the synthesis of ortho-olefinated biaryls. This has been achieved through an atom-economic threefold cross-coupling of triarylbismuth reagents with 2-halobenzaldehydes followed by pot-economic in situ Wittig olefination. The overall process is a pot-economic straightforward synthesis of ortho-olefinated biaryls from 2-halobenzaldehydes, triarylbismuth reagents and phosphonium salts. This pot-economic approach was applied to the formal synthesis of medicinally important Eupomatilone-6.

A new synthetic approach to 6-unsubstituted phenanthridine and phenanthridine-like compounds under mild and metal-free conditions

Tummatorn, Jumreang,Krajangsri, Suppachai,Norseeda, Krissada,Thongsornkleeb, Charnsak,Ruchirawat, Somsak

supporting information, p. 5077 - 5081 (2014/07/08)

A new and mild synthetic approach for the synthesis of 6-unsubstituted phenanthridine and phenanthridine-like compounds under metal-free conditions at room temperature has been developed. The strategy involved a tandem azide rearrangement/intramolecular annulation and oxidation reactions of biarylmethyl azide precursors to obtain the desired products in up to 99% yields with high regioselectivity.

Synthesis of novel 7-oxo and 7-hydroxy trifluoroallocolchicinoids with cytotoxic effect

Chosson, Elizabeth,Santoro, Francesca,Rochais, Christophe,Santos, Jana Sopkova-De Oliveira,Legay, Rémi,Thoret, Sylviane,Cresteil, Thierry,Sinicropi, Maria Stefania,Besson, Thierry,Dallemagne, Patrick

experimental part, p. 2614 - 2623 (2012/06/01)

The synthesis of 7-oxo and 7-hydroxy trifluoroallocolchicinoids was achieved through the intramolecular cyclization of o-phenyl-β- phenylalanines. The resulting compounds were evaluated for their cytotoxic activity against KB cells and their inhibitory ef

One-Pot Zn/CuI/TFA-catalyzed domino three-component-carbocyclization reaction involving Biphenyl-2-carbaldehydes/Alkynes/Piperidine: Allenes-mediated construction of phenanthrenes

Saifuddin, Mohammad,Agarwal, Piyush K.,Kundu, Bijoy

experimental part, p. 10122 - 10128 (2012/02/05)

A one-pot protocol involving Zn/CuI/TFA-catalyzed domino three-component and subsequent carbocyclization reactions is described. The reaction proceeds via formation of propargyl amines from biphenyl-2-carbaldehydes/terminal alkynes/piperidine followed by

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