Welcome to LookChem.com Sign In|Join Free
  • or
Methyl 5-bromopyridin-2-ylcarbamate is a chemical compound with the molecular formula C7H7BrN2O2. It is characterized by the presence of a carbamate group, which involves a carbon atom doubly bonded to an oxygen atom and single-bonded to a nitrogen atom, and a methyl group, which contains one carbon atom bonded to three hydrogen atoms. Methyl 5-bromopyridin-2-ylcarbamate also features a bromopyridinyl group, essentially a pyridine ring with a bromine atom attached, specifically at the 5 position of the ring.

207922-56-3

Post Buying Request

207922-56-3 Suppliers

Recommended suppliers

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

207922-56-3 Usage

Uses

Used in Chemical Synthesis:
Methyl 5-bromopyridin-2-ylcarbamate is used as a building block for the synthesis of various chemical products. Its unique structure allows it to be incorporated into a wide range of molecules, making it a valuable component in the creation of new compounds.
Used in Chemical Reactions:
Methyl 5-bromopyridin-2-ylcarbamate is used as a reagent in chemical reactions. Its carbamate and bromopyridinyl groups can participate in various chemical transformations, facilitating the production of desired products in the synthesis process.
Used in Pharmaceutical Industry:
Methyl 5-bromopyridin-2-ylcarbamate is used as an intermediate in the synthesis of pharmaceutical compounds. Its presence in the molecular structure can contribute to the development of new drugs with potential therapeutic applications.
Used in Research and Development:
Methyl 5-bromopyridin-2-ylcarbamate is used as a research compound in the study of chemical reactions and synthesis pathways. Its properties and reactivity can provide valuable insights into the development of new synthetic methods and the understanding of chemical behavior.

Check Digit Verification of cas no

The CAS Registry Mumber 207922-56-3 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 2,0,7,9,2 and 2 respectively; the second part has 2 digits, 5 and 6 respectively.
Calculate Digit Verification of CAS Registry Number 207922-56:
(8*2)+(7*0)+(6*7)+(5*9)+(4*2)+(3*2)+(2*5)+(1*6)=133
133 % 10 = 3
So 207922-56-3 is a valid CAS Registry Number.

207922-56-3SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 13, 2017

Revision Date: Aug 13, 2017

1.Identification

1.1 GHS Product identifier

Product name methyl N-(5-bromopyridin-2-yl)carbamate

1.2 Other means of identification

Product number -
Other names 5-BROMO-2-(METHOXYCARBONYLAMINO)PYRIDINE

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:207922-56-3 SDS

207922-56-3Downstream Products

207922-56-3Relevant academic research and scientific papers

Tandem Condensation/Rearrangement Reaction of 2-Aminohetarene N-Oxides for the Synthesis of Hetaryl Carbamates

Bystrov, Dmitry M.,Zhilin, Egor S.,Fershtat, Leonid L.,Romanova, Anna A.,Ananyev, Ivan V.,Makhova, Nina N.

, p. 3157 - 3163 (2018/08/24)

A new approach to hetaryl carbamates through a tandem condensation/rearrangement reaction of 2-aminohetarene N-oxides was developed. The developed reaction is suitable for both five- and six-membered heterocycles and proceeds through the condensation of 2

Chloroformate free, scalable approach for the synthesis of organic carbamates and their alkylation

Shewalkar, Mukesh P.,Rao, Ramakrishna R.,Reddy, Veerbhadra,Darandale, Sunil N.,Shinde, Devanand B.

, p. 60 - 64 (2013/07/26)

A convenient method for the synthesis of organic carbamates of 2-aminopyridine without using hazardous chloroformate reagent is developed. This alternate approach for the synthesis of organic carbamates and their alkylation to 2-alkylaminopyridines is more practical and economical to be used on large scale. The amazing behavior of 2- aminopyridine helps in forming organic carbamates unlike 3-aminopyridine and 4-aminopyridine.

Process for substituted pyridines

-

, (2008/06/13)

This invention relates to processes for preparing compounds of the formula (I) and to processes for preparing certain intermediates of the formula wherein R1is nitro, amino or protected amino; R2is H, fluoro, chloro CF3, n

BETA-ADRENERGIC AGONISTS TO REDUCE A WASTING CONDITION

-

, (2008/06/13)

The present invention relates to the use of certain β-adrenergic agonists to reduce a wasting condition in a mammal (e.g., human).

Beta-Adrenergic agonists to reduce a wasting condition

-

, (2008/06/13)

The present invention relates to the use of certain β-adrenergic agonists, their pharmaceutically acceptable prodrugs, pharmaceutically acceptable salts of either entity, or pharmaceutical compositions containing any of the foregoing, for the manufacture

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 207922-56-3