Welcome to LookChem.com Sign In|Join Free
  • or
2-Bromoacrylamide, with the molecular formula C3H4BrNO, is a white crystalline solid that serves as a versatile intermediate in the synthesis of pharmaceuticals, agrochemicals, and other organic compounds. Its reactivity towards various nucleophiles and electrophiles makes it a valuable building block for the preparation of a range of functionalized compounds. Additionally, it can be used as a monomer in the production of polymers and copolymers. However, it is important to note that 2-Bromoacrylamide is toxic and can cause irritation upon contact with skin or eyes, and inhalation of its vapors, necessitating proper safety precautions during handling.

70321-36-7

Post Buying Request

70321-36-7 Suppliers

Recommended suppliers

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

70321-36-7 Usage

Uses

Used in Pharmaceutical Industry:
2-Bromoacrylamide is used as a key intermediate in the synthesis of various pharmaceutical compounds. Its reactivity allows for the creation of a wide range of functionalized molecules, making it a valuable component in the development of new drugs and therapeutic agents.
Used in Agrochemical Industry:
In the agrochemical industry, 2-Bromoacrylamide is utilized as an intermediate for the synthesis of various agrochemicals, including pesticides and herbicides. Its ability to react with different nucleophiles and electrophiles enables the production of a diverse array of active ingredients for agricultural applications.
Used in Polymer and Copolymer Production:
2-Bromoacrylamide is used as a monomer in the production of polymers and copolymers. Its reactivity contributes to the formation of polymers with specific properties, making it a useful component in the development of materials for various applications, such as coatings, adhesives, and plastics.
Used in Organic Synthesis:
As a versatile building block, 2-Bromoacrylamide is used in organic synthesis for the preparation of a variety of functionalized compounds. Its reactivity towards nucleophiles and electrophiles allows for the creation of complex molecules with specific properties, making it a valuable tool in the synthesis of organic compounds for research and industrial applications.

Check Digit Verification of cas no

The CAS Registry Mumber 70321-36-7 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 7,0,3,2 and 1 respectively; the second part has 2 digits, 3 and 6 respectively.
Calculate Digit Verification of CAS Registry Number 70321-36:
(7*7)+(6*0)+(5*3)+(4*2)+(3*1)+(2*3)+(1*6)=87
87 % 10 = 7
So 70321-36-7 is a valid CAS Registry Number.

70321-36-7SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 16, 2017

Revision Date: Aug 16, 2017

1.Identification

1.1 GHS Product identifier

Product name 2-bromoprop-2-enamide

1.2 Other means of identification

Product number -
Other names 2-bromoacrylic acid amide

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:70321-36-7 SDS

70321-36-7Upstream product

70321-36-7Relevant academic research and scientific papers

How Reaction Conditions May Influence the Regioselectivity in the Synthesis of 2,3-Dihydro-1,4-benzoxathiine Derivatives

Casiraghi, Andrea,Valoti, Ermanno,Suigo, Lorenzo,Artasensi, Angelica,Sorvillo, Erica,Straniero, Valentina

, p. 13217 - 13227 (2018/10/24)

The exploration of different reaction conditions aiming to obtain both 2,3-dihydro-1,4-benzoxathiine-2-yl derivatives and 2,3-dihydro-1,4-benzoxathiine-3-yl ones is reported. The treatment of 1,2-mercaptophenol with an organic base and a specific 2-bromo acrylate results in a solvent- and substrate-dependent exclusive solvation of O- and S-anions, thus managing the regioselectivity.

Reaction of amides of 2,3-dibromopropionic and 2-bromoacrylic acids with pyridine and triphenylphosphine

Khachikyan,Tovmasyan,Indzhikyan

experimental part, p. 759 - 761 (2009/09/26)

By refluxing pyridine with 2,3-dibromopropionic acid amide in acetonitrile, amide of 3-bromo-2-pyridiniumbromidopropionic acid I was synthesized. The latter is inert toward the second molecule of pyridine under the used conditions. Compound I was found to

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 70321-36-7