Welcome to LookChem.com Sign In|Join Free

CAS

  • or
2,2-Difluoro-1,3-benzodioxole-5-carbonyl chloride is a chemical compound that is primarily recognized for its use in the production of other chemicals. It contains carbon, hydrogen, chlorine, oxygen, and fluorine, exhibiting a unique blend of properties that make it valuable in various chemical processes. However, there is limited publicly available information on its properties such as boiling point, melting point, and density. 2,2-Difluoro-1,3-benzodioxole-5-carbonyl chloride is understood to be hazardous, necessitating careful handling and storage to avoid risks associated with exposure or inadvertent reactions with incompatible substances. It is also crucial to use this chemical in areas with proper ventilation for safety precautions.

127163-51-3

Post Buying Request

127163-51-3 Suppliers

Recommended suppliersmore

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

127163-51-3 Usage

Uses

Used in Chemical Synthesis:
2,2-Difluoro-1,3-benzodioxole-5-carbonyl chloride is used as a chemical intermediate for the synthesis of various other chemicals. Its unique structure and properties make it a valuable component in the creation of new compounds with potential applications in different industries.
Used in Pharmaceutical Industry:
In the pharmaceutical industry, 2,2-Difluoro-1,3-benzodioxole-5-carbonyl chloride is used as a key building block for the development of new drugs. Its chemical properties allow for the formation of complex molecules that can target specific biological pathways, potentially leading to the discovery of novel therapeutic agents.
Used in Material Science:
2,2-Difluoro-1,3-benzodioxole-5-carbonyl chloride is used as a precursor in the development of new materials with specific properties. Its incorporation into polymers or other materials can result in enhanced characteristics such as improved stability, reactivity, or selectivity, which can be beneficial in various applications.
Used in Research and Development:
In research and development settings, 2,2-Difluoro-1,3-benzodioxole-5-carbonyl chloride is used as a versatile compound for exploring new chemical reactions and pathways. Its reactivity and structural features make it an interesting subject for studying the mechanisms of chemical transformations and the development of new synthetic strategies.

Check Digit Verification of cas no

The CAS Registry Mumber 127163-51-3 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,2,7,1,6 and 3 respectively; the second part has 2 digits, 5 and 1 respectively.
Calculate Digit Verification of CAS Registry Number 127163-51:
(8*1)+(7*2)+(6*7)+(5*1)+(4*6)+(3*3)+(2*5)+(1*1)=113
113 % 10 = 3
So 127163-51-3 is a valid CAS Registry Number.
InChI:InChI=1/C8H3ClF2O3/c9-7(12)4-1-2-5-6(3-4)14-8(10,11)13-5/h1-3H

127163-51-3SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 20, 2017

Revision Date: Aug 20, 2017

1.Identification

1.1 GHS Product identifier

Product name 2,2-Difluoro-1,3-benzodioxole-5-carbonyl chloride

1.2 Other means of identification

Product number -
Other names 2,2-difluorobenzo[d][1,3]dioxole-5-carbonyl chloride

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:127163-51-3 SDS

127163-51-3Downstream Products

127163-51-3Relevant articles and documents

Diastereoselective olefin amidoacylationviaphotoredox PCET/nickel-dual catalysis: reaction scope and mechanistic insights

Anna, Jessica M.,Hong, Xin,Molander, Gary A.,Saeednia, Borna,Zhang, Shuo-Qing,Zheng, Shuai,Zhou, Jiawang

, p. 4131 - 4137 (2020)

The selective 1,2-aminoacylation of olefins provides opportunities for the rapid construction of nitrogen-containing molecules. However, the lack of CO-free acylation reactions has limited their application. By using photoredox proton-coupled electron transfer (PCET)/Ni dual-catalysis, a highly regio- and diastereoselective amidoacylation of unactivated olefins has been developed. Various acyl electrophiles are compatible, including alkyl- and aryl acyl chlorides and anhydrides, as well asin situactivated carboxylic acids. Hammett studies and other mechanistic experiments to elucidate features of the diastereoselectivity, a transient absorption study of the PCET step, as well as computational evidence, provide an in-depth understanding of the disclosed transformation.

PIPERONYLIC ACID DERIVATIVE AND PREPARATION AND APPLICATION THEREOF

-

Paragraph 0108-0110; 0112; 0124; 0127, (2020/07/05)

The present invention belongs to the fields of insecticides, acaricides and fungicides, and particularly relates to a piperonylic acid derivative, and preparation and application thereof. The structure is shown in a general formula I, and the definition o

A Direct Approach to Decoration of Bioactive Compounds via C-H Amination Reaction

Ju, Guodong,Yuan, Chunchen,Wang, Dongjie,Zhang, Jingyu,Zhao, Yingsheng

supporting information, p. 9852 - 9855 (2019/12/24)

The development of new methods to achieve the direct synthesis of bioactive organic molecules is always an important topic in organic synthesis. We hereby demonstrate that N-methoxyamide is an excellent amino source in the iridium-catalyzed intermolecular C-H amination reaction. The linkage of two bioactive organic molecules can be well achieved with this new protocol. More than 20 examples of decorated bioactive compounds were reported, which can facilitate the discovery of new bioactive molecules.

Ramoplanin derivatives possessing antibacterial activity

-

Page/Page column 66, (2010/11/23)

Novel ramoplanin derivatives are disclosed. These ramoplanin derivatives exhibit antibacterial activity. As the compounds of the subject invention exhibit potent activities against gram positive bacteria, they are useful antimicrobial agents. Methods of synthesis and of use of the compounds are also disclosed.

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

What can I do for you?
Get Best Price

Get Best Price for 127163-51-3