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CAS

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2416-02-6

3'-Bromo-2,2-dimethylpropiophenone is an organic chemical compound with the molecular formula C12H15BrO. It is a derivative of propiophenone, featuring a bromine atom at the 3' position, and two methyl groups attached to the carbon adjacent to the carbonyl group. 3'-bromo-2,2-dimethylpropiophenone is a colorless to pale yellow liquid with a pungent odor. It is primarily used as an intermediate in the synthesis of various pharmaceuticals, agrochemicals, and other organic compounds. Due to its reactivity, it is essential to handle 3'-bromo-2,2-dimethylpropiophenone with care, following proper safety protocols and guidelines.

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  • 2416-02-6 Structure

  • Basic information

    1. Product Name: 3'-BROMO-2,2-DIMETHYLPROPIOPHENONE
    2. Synonyms: 3'-BROMO-2,2-DIMETHYLPROPIOPHENONE
    3. CAS NO:2416-02-6
    4. Molecular Formula: C11H13BrO
    5. Molecular Weight: 241.12
    6. EINECS: N/A
    7. Product Categories: N/A
    8. Mol File: 2416-02-6.mol

  • Chemical Properties

    1. Melting Point: N/A
    2. Boiling Point: N/A
    3. Flash Point: N/A
    4. Appearance: /
    5. Density: N/A
    6. Refractive Index: N/A
    7. Storage Temp.: N/A
    8. Solubility: N/A
    9. CAS DataBase Reference: 3'-BROMO-2,2-DIMETHYLPROPIOPHENONE(CAS DataBase Reference)
    10. NIST Chemistry Reference: 3'-BROMO-2,2-DIMETHYLPROPIOPHENONE(2416-02-6)
    11. EPA Substance Registry System: 3'-BROMO-2,2-DIMETHYLPROPIOPHENONE(2416-02-6)

  • Safety Data

    1. Hazard Codes: N/A
    2. Statements: N/A
    3. Safety Statements: N/A
    4. WGK Germany:
    5. RTECS:
    6. HazardClass: N/A
    7. PackingGroup: N/A
    8. Hazardous Substances Data: 2416-02-6(Hazardous Substances Data)

2416-02-6 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 2416-02-6 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 2,4,1 and 6 respectively; the second part has 2 digits, 0 and 2 respectively.
Calculate Digit Verification of CAS Registry Number 2416-02:
(6*2)+(5*4)+(4*1)+(3*6)+(2*0)+(1*2)=56
56 % 10 = 6
So 2416-02-6 is a valid CAS Registry Number.

2416-02-6SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 18, 2017

Revision Date: Aug 18, 2017

1.Identification

1.1 GHS Product identifier

Product name 1-(3-bromophenyl)-2,2-dimethylpropan-1-one

1.2 Other means of identification

Product number -
Other names 3'-bromo-2,2-dimethylpropiophenone

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:2416-02-6 SDS

2416-02-6Relevant articles and documents

Light-DrivenN-Heterocyclic Carbene Catalysis Using Alkylborates

Sato, Yukiya,Goto, Yamato,Nakamura, Kei,Miyamoto, Yusuke,Sumida, Yuto,Ohmiya, Hirohisa

, p. 12886 - 12892 (2021/10/29)

Radical-radical coupling, the selective reaction between two different radical species, has contributed to the methodology for connecting bulky units. Light-drivenN-heterocyclic carbene (NHC) organocatalysis is recognized as a state-of-the-art methodology enabling radical-radical coupling. The catalytic process involves forming an acyl azolium intermediate from the NHC catalyst and an acyl donor, followed by single electron reduction of this key intermediate, which is largely dependent on the photoredox catalyst. We designed a radical NHC catalysis in which the direct photoexcitation of a borate to form a high reducing agent facilitated the single electron reduction event. The borate produces an alkyl radical for the single electron transfer process to accomplish the radical-radical coupling. This protocol enables cross-coupling between alkylborates and acyl imidazoles in addition to radical relay-type alkylacylations of alkenes with alkylborates and acyl imidazoles, affording ketones with a broad scope.

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