Welcome to LookChem.com Sign In|Join Free
  • or
1-(5-BROMO-4-CHLORO-2-THIENYL)ETHANONE, also known as ethanone, is an organic compound characterized by the chemical formula C6H4BrClOS. It is a yellow solid with a distinctive strong odor. This ketone features a thienyl group, which is integral to its role as an intermediate in the synthesis of pharmaceuticals and agrochemicals. Due to its chemical properties, it is a valuable precursor in the production of various drugs and pesticides. However, it is crucial to handle 1-(5-BROMO-4-CHLORO-2-THIENYL)ETHANONE with care, as it can pose hazards if not used properly, necessitating the implementation of appropriate safety measures.

123418-66-6

Post Buying Request

123418-66-6 Suppliers

Recommended suppliers

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

123418-66-6 Usage

Uses

Used in Pharmaceutical Industry:
1-(5-BROMO-4-CHLORO-2-THIENYL)ETHANONE is used as a synthetic intermediate for the development of various pharmaceuticals. Its unique structure, including the thienyl group, allows for the creation of a wide range of medicinal compounds, contributing to the advancement of treatments for different health conditions.
Used in Agrochemical Industry:
In the agrochemical sector, 1-(5-BROMO-4-CHLORO-2-THIENYL)ETHANONE is utilized as a key intermediate in the synthesis of pesticides. Its chemical properties make it suitable for the production of effective pest control agents, thereby supporting agricultural productivity and crop protection.

Check Digit Verification of cas no

The CAS Registry Mumber 123418-66-6 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,2,3,4,1 and 8 respectively; the second part has 2 digits, 6 and 6 respectively.
Calculate Digit Verification of CAS Registry Number 123418-66:
(8*1)+(7*2)+(6*3)+(5*4)+(4*1)+(3*8)+(2*6)+(1*6)=106
106 % 10 = 6
So 123418-66-6 is a valid CAS Registry Number.

123418-66-6SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 13, 2017

Revision Date: Aug 13, 2017

1.Identification

1.1 GHS Product identifier

Product name 1-(5-Bromo-4-chlorothiophen-2-yl)ethanone

1.2 Other means of identification

Product number -
Other names 1-(5-Bromo-4-chloro-2-thienyl)ethanone

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:123418-66-6 SDS

123418-66-6Relevant academic research and scientific papers

2-METHYL-QUINAZOLINES

-

Page/Page column 371, (2018/10/19)

The present invention describes 2-methyl-quinazoline compounds of general formula (I), methods of preparing said compounds, intermediate compounds useful for preparing said compounds, pharmaceutical compositions and combinations comprising said compounds, and the use of said compounds for manufacturing pharmaceutical compositions. The 2-methyl substituted quinazoline compounds of general formula(I) effectively and selectively inhibit the Ras-Sos interaction without significantly targeting the EGFR receptor. They are therefore useful for the treatment or prophylaxis of diseases, in particular of hyperproliferative disorders, such as cancer as a sole agent or in combination with other active ingredients.

INHIBITORS OF Akt ACTIVITY

-

Page/Page column 142, (2010/11/27)

Invented are novel thiophene compounds, the use of such compounds as inhibitors of protein kinase B activity and in the treatment of cancer and arthritis.

Herbicidal Thienylureas, I

Stanetty, Peter,Puschautz, Erhard,Friedbacher, Gernot

, p. 53 - 63 (2007/10/02)

Syntheses of the title substances as potential herbicides are described by a modified Curtius degradation of corresponding thiophene carboxylic acids, obtained in turn by haloform reaction of appropriate acetyl thiophenes.Regioselective substitution reactions of thiophenes were key steps for the construction of desired substitution patterns.Structure-activity considerations show that especially the 3-thienyl ureas 36 and 38 exhibit significant herbicidal activity comparable with commercial products. - Keywords: Curtius degradation; Herbicides; Thiophenes; Ureas; Urethanes

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 123418-66-6