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7506-49-2

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7506-49-2 Usage

Description

(3-methylphenyl) 4-nitrobenzoate, also known as methyl 4-nitrobenzoate, is a chemical compound with the molecular formula C14H11NO4. It is a nitrobenzoate ester, consisting of a 4-nitrobenzoate group and a 3-methylphenyl group. This yellow crystalline solid is sparingly soluble in water but soluble in organic solvents. Its unique chemical structure and properties make it a promising candidate for various applications in organic synthesis and pharmaceutical development.

Uses

Used in Organic Synthesis:
(3-methylphenyl) 4-nitrobenzoate is used as an intermediate in the synthesis of various organic compounds. Its versatile structure allows for the creation of a wide range of derivatives, making it a valuable building block in the development of new chemical entities.
Used in Pharmaceutical Production:
As an intermediate, (3-methylphenyl) 4-nitrobenzoate plays a crucial role in the production of pharmaceuticals. Its unique structure can be utilized to develop new drugs with potential therapeutic benefits.
Used in Dye Manufacturing:
(3-methylphenyl) 4-nitrobenzoate is also used in the manufacturing of dyes. Its chemical properties contribute to the formation of dyes with specific color characteristics, making it an important component in the dye industry.
Used in Drug Discovery:
Due to its unique chemical structure, (3-methylphenyl) 4-nitrobenzoate may have potential uses in drug discovery. Researchers can explore its properties to identify new therapeutic agents or improve existing ones.
Used in Chemical Research:
(3-methylphenyl) 4-nitrobenzoate serves as a valuable compound in chemical research. Its properties can be studied to gain insights into the behavior of similar chemical entities, contributing to the broader understanding of organic chemistry.

Check Digit Verification of cas no

The CAS Registry Mumber 7506-49-2 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 7,5,0 and 6 respectively; the second part has 2 digits, 4 and 9 respectively.
Calculate Digit Verification of CAS Registry Number 7506-49:
(6*7)+(5*5)+(4*0)+(3*6)+(2*4)+(1*9)=102
102 % 10 = 2
So 7506-49-2 is a valid CAS Registry Number.
InChI:InChI=1/C14H11NO4/c1-10-3-2-4-13(9-10)19-14(16)11-5-7-12(8-6-11)15(17)18/h2-9H,1H3

7506-49-2SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 17, 2017

Revision Date: Aug 17, 2017

1.Identification

1.1 GHS Product identifier

Product name (3-methylphenyl) 4-nitrobenzoate

1.2 Other means of identification

Product number -
Other names m-tolyl 4-nitrobenzoate

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:7506-49-2 SDS

7506-49-2Relevant articles and documents

Pd(II)-catalyzed C-H activation/aryl-aryl coupling of phenol esters

Xiao, Bin,Fu, Yao,Xu, Jun,Gong, Tian-Jun,Dai, Jian-Jun,Yi, Jun,Liu, Lei

supporting information; experimental part, p. 468 - 469 (2010/03/25)

(Chemical Equation Presented) Although nitrogen-containing group-directed cyclopalladation reactions have been well-known, Pd(II) insertion into C-H bonds promoted by coordination of an oxygen-only group to the palladium remains rather rare. In the present study, the first cyclopalladation complex formed from a simple phenol ester was characterized by X-ray crystallography. A promising protocol for the ortho C-H activation/aryl-aryl coupling of phenol esters that was not sensitive to moisture or air was then established. The utility of the reaction was demonstrated for the synthesis of useful phenol derivatives. Copyright

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