Welcome to LookChem.com Sign In|Join Free
  • or
N-BROMOCAPROLACTAM, with the molecular formula C6H10BrNO, is a brominated derivative of caprolactam. It is a chemical compound that serves as a crucial intermediate in the synthesis of various polymers and resins, particularly polyamide-based materials such as nylon. Its unique structure and properties make it a valuable building block in the production of specialty polymers and a reagent in organic synthesis. However, due to its irritant and sensitizing properties, it requires careful handling in a controlled laboratory environment.

2439-83-0

Post Buying Request

2439-83-0 Suppliers

Recommended suppliers

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

2439-83-0 Usage

Uses

Used in Polymer and Resin Production:
N-BROMOCAPROLACTAM is used as an intermediate for the production of certain polymers and resins. It plays a vital role in the synthesis process, contributing to the formation of the desired polymeric materials.
Used in Nylon Manufacturing:
N-BROMOCAPROLACTAM is used as a building block in the synthesis of polyamide-based materials, including nylon. Its presence in the manufacturing process helps create the characteristic properties of nylon, such as strength, durability, and flexibility.
Used in Specialty Polymer Production:
N-BROMOCAPROLACTAM is used as a key component in the manufacturing of specialty polymers. These polymers often possess unique properties tailored for specific applications, and the compound contributes to their development and performance.
Used in Organic Synthesis as a Reagent:
N-BROMOCAPROLACTAM is used as a reagent in organic synthesis. Its chemical properties allow it to participate in various reactions, facilitating the formation of desired products in organic chemistry.
Used in Laboratory Research:
N-BROMOCAPROLACTAM is used in laboratory research for the development of new materials and the study of its chemical properties. Its unique structure and reactivity make it a valuable subject for scientific investigation.

Check Digit Verification of cas no

The CAS Registry Mumber 2439-83-0 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 2,4,3 and 9 respectively; the second part has 2 digits, 8 and 3 respectively.
Calculate Digit Verification of CAS Registry Number 2439-83:
(6*2)+(5*4)+(4*3)+(3*9)+(2*8)+(1*3)=90
90 % 10 = 0
So 2439-83-0 is a valid CAS Registry Number.
InChI:InChI=1/C6H10BrNO/c7-8-5-3-1-2-4-6(8)9/h1-5H2

2439-83-0SDS

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 N-BROMOCAPROLACTAM

1.2 Other means of identification

Product number -
Other names N-Bromo-epsilon-caprolactam

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:2439-83-0 SDS

2439-83-0Upstream product

2439-83-0Downstream Products

2439-83-0Relevant academic research and scientific papers

Conversion of nucleophilic halides to electrophilic halides: Efficient and selective halogenation of azinones, amides, and carbonyl compounds using metal halide/lead tetraacetate

Kim, Jeum-Jong,Kweon, Deok-Heon,Cho, Su-Dong,Kim, Ho-Kyun,Lee, Sang-Gyeong,Yoon, Yong-Jin

, p. 194 - 200 (2007/10/03)

AlCl3/Pb(OAc)4 and ZnBr2/Pb(OAc) 4 are efficient electrophilic N- and α-C-halogenating agents. A variety of azinones, amides and carbonyl compounds were chemoselectively and regioselectively N-, or α-C-halogenated in good to excellent yield using AlCl3/Pb(OAc)4 and ZnBr2/Pb(OAc)4 in acetonitrile. Georg Thieme Verlag Stuttgart.

A Practical Synthesis of N-Bromo Imides by Use of Sodium Bromite

Kajigaeshi, Shoji,Nakagawa, Takashi,Fujisaki, Shizuo,Nishida, Akiko

, p. 769 - 770 (2007/10/02)

N-Bromo imides can be readily prepared under mild conditions by a reaction of imides with sodium bromite in the presence of hydrobromic acid in fairly good yields.The scope and limitation are also presented.

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 2439-83-0