Welcome to LookChem.com Sign In|Join Free
  • or
Methyl 2-(nitromethyl)benzoate is an organic compound with the chemical formula C9H9NO4. It is a derivative of benzoic acid, where a methyl group is attached to the benzene ring at the 2nd position, and a nitromethyl group is also attached to the same carbon. methyl 2-(nitromethyl)benzoate is characterized by its yellowish color and is soluble in organic solvents. It is synthesized through a reaction involving benzoic acid and nitroalkanes, and is used in the preparation of various pharmaceuticals and chemical intermediates. Due to its reactivity, it is important to handle methyl 2-(nitromethyl)benzoate with care, as it can undergo further chemical transformations, such as reduction to form aminomethylbenzoate derivatives.

5025-49-0

Post Buying Request

5025-49-0 Suppliers

Recommended suppliers

  • Product
  • FOB Price
  • Min.Order
  • Supply Ability
  • Supplier
  • Contact Supplier

5025-49-0 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 5025-49-0 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 5,0,2 and 5 respectively; the second part has 2 digits, 4 and 9 respectively.
Calculate Digit Verification of CAS Registry Number 5025-49:
(6*5)+(5*0)+(4*2)+(3*5)+(2*4)+(1*9)=70
70 % 10 = 0
So 5025-49-0 is a valid CAS Registry Number.

5025-49-0SDS

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 2-(nitromethyl)benzoate

1.2 Other means of identification

Product number -
Other names -

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:5025-49-0 SDS

5025-49-0Relevant academic research and scientific papers

Minimizing the amount of nitromethane in palladium-catalyzed cross-coupling with aryl halides

Walvoord, Ryan R.,Kozlowski, Marisa C.

, p. 8859 - 8864 (2013/09/24)

A method for the formation of arylnitromethanes is described that employs readily available aryl halides or triflates and small amounts of nitromethane in a dioxane solvent, thereby reducing the hazards associated with this reagent. Specifically, 2-10 equiv (1-5% v/v) of nitromethane can be employed in comparison to prior work that used nitromethane as solvent (185 equiv). The present transformation provides high yields at relatively low temperatures and tolerates an array of functionality, including heterocycles and substantial steric encumbrance.

Post a RFQ

Enter 15 to 2000 letters.Word count: 0 letters

Attach files(File Format: Jpeg, Jpg, Gif, Png, PDF, PPT, Zip, Rar,Word or Excel Maximum File Size: 3MB)

1 Customer Service

What can I do for you?
Get Best Price

Get Best Price for 5025-49-0