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728919-26-4

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728919-26-4 Usage

Description

3-(6-(Methoxycarbonyl)naphthalen-2-yl)benzaldehyde is a chemical compound with a molecular formula of C23H16O3. It features a benzaldehyde group attached to a naphthalene ring, with a methoxycarbonyl substituent at the 6-position. 3-(6-(Methoxycarbonyl)naphthalen-2-yl)benzaldehyde is known for its potential applications in organic synthesis, pharmaceutical industry, and medicinal chemistry.

Uses

Used in Organic Synthesis:
3-(6-(Methoxycarbonyl)naphthalen-2-yl)benzaldehyde is used as a building block or intermediate for the synthesis of various organic compounds. Its unique structure allows for the creation of a wide range of molecules with diverse properties and applications.
Used in Pharmaceutical Industry:
In the pharmaceutical industry, 3-(6-(Methoxycarbonyl)naphthalen-2-yl)benzaldehyde is utilized for the production of various drugs and pharmaceuticals. Its specific chemical structure and properties make it a valuable component in the development of new medications.
Used in Medicinal Chemistry:
3-(6-(Methoxycarbonyl)naphthalen-2-yl)benzaldehyde holds significant value in the field of medicinal chemistry. It is employed in the creation of novel pharmaceuticals, potentially leading to breakthroughs in the treatment of various diseases and conditions.
Used in Material Development:
3-(6-(Methoxycarbonyl)naphthalen-2-yl)benzaldehyde also has potential applications in the development of new materials and compounds for various industrial and research purposes. Its unique structure and properties can contribute to the advancement of materials science and technology.
The precise properties and applications of 3-(6-(Methoxycarbonyl)naphthalen-2-yl)benzaldehyde may depend on its specific chemical structure and purity level, making it a versatile and valuable compound in multiple fields.

Check Digit Verification of cas no

The CAS Registry Mumber 728919-26-4 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 7,2,8,9,1 and 9 respectively; the second part has 2 digits, 2 and 6 respectively.
Calculate Digit Verification of CAS Registry Number 728919-26:
(8*7)+(7*2)+(6*8)+(5*9)+(4*1)+(3*9)+(2*2)+(1*6)=204
204 % 10 = 4
So 728919-26-4 is a valid CAS Registry Number.

728919-26-4SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 19, 2017

Revision Date: Aug 19, 2017

1.Identification

1.1 GHS Product identifier

Product name methyl 6-(3-formylphenyl)naphthalene-2-carboxylate

1.2 Other means of identification

Product number -
Other names Benzaldehyde,3-(2-naphthalenyl)

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:728919-26-4 SDS

728919-26-4Downstream Products

728919-26-4Relevant articles and documents

The 1,3-diaminobenzene-derived aminophosphine palladium pincer complex {C6H3[NHP(piperidinyl)2]2Pd(Cl)} - A highly active Suzuki-Miyaura catalyst with excellent functional group tolerance

Bolliger, Jeanne L.,Frech, Christian M.

experimental part, p. 1075 - 1080 (2010/06/17)

The rapidly prepared 1,3-diaminobenzenederived aminophosphine pincer complex {C6H3 [NHP(piperidinyl)2] 2Pd(Cl)} (1) is an effective Suzuki catalyst with excellent functional group tolerance. Side-product formations, such as homocoupling, debromation or protodeboration have only rarely been detected and if so, were in all cases below the 5% level. The presented reaction protocol is universally applicable. Experimental observations indicate that palladium nanoparticles are the catalytically active form of 1.

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