Welcome to LookChem.com Sign In|Join Free

CAS

  • or

129053-70-9

Post Buying Request

129053-70-9 Suppliers

Recommended suppliersmore

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

129053-70-9 Usage

General Description

2-Bromo-5-phenyl-1,3-oxazole is a chemical compound with the molecular formula C9H6BrNO. It is an oxazole derivative with a bromo-substituted phenyl group attached to the 5-position of the oxazole ring. 2-bromo-5-phenyl-1,3-oxazole is used in organic synthesis and medicinal chemistry as a building block for the synthesis of various pharmaceuticals and biologically active molecules. It has also been studied for its potential anti-inflammatory and antimicrobial properties. 2-Bromo-5-phenyl-1,3-oxazole is a versatile compound with potential applications in a range of research and industrial fields.

Check Digit Verification of cas no

The CAS Registry Mumber 129053-70-9 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,2,9,0,5 and 3 respectively; the second part has 2 digits, 7 and 0 respectively.
Calculate Digit Verification of CAS Registry Number 129053-70:
(8*1)+(7*2)+(6*9)+(5*0)+(4*5)+(3*3)+(2*7)+(1*0)=119
119 % 10 = 9
So 129053-70-9 is a valid CAS Registry Number.
InChI:InChI=1/C9H6BrNO/c10-9-11-6-8(12-9)7-4-2-1-3-5-7/h1-6H

129053-70-9SDS

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 2-Bromo-5-phenyl-1,3-oxazole

1.2 Other means of identification

Product number -
Other names 2-bromo-5-phenyloxazole

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:129053-70-9 SDS

129053-70-9Downstream Products

129053-70-9Relevant articles and documents

A simple base-mediated halogenation of acidic sp2 C-H bonds under noncryogenic conditions

Do, Hien-Quang,Daugulis, Olafs

supporting information; experimental part, p. 421 - 423 (2009/07/04)

(Chemical Equation Presented) A new method has been developed for in situ halogenation of acidic sp2 carbon-hydrogen bonds in heterocycles and electron-deficient arenes. Either selective monohalogenation or one-step exhaustive polyhalogenation is possible for substrates possessing several C-H bonds that are flanked by electron-withdrawing groups. For the most acidic arenes, such as pentafluorobenzene, K3PO4 base can be employed instead of BuLi for metalation/halogenation sequences.

SPECTROMETRIE DE MASSE DE TRIAZOLIDES ET DE LEURS PRODUITS DE TRANSFORMATION PAR PYROLYSE-ECLAIR SOUS VIDE

Maquestiau, Andre,Abdelouahab, Fouad Bachir Ben,Flammang, Robert

, p. 89 - 101 (2007/10/02)

Besides the formation of acylium ions, the molecular ions of 1-acyl-1,2,4-triazoles substituted (R) at position 3 lose competitively ketene and carbon monoxide after electron impact ionization, but the ketene loss dominates largely if R is a strong electr

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 129053-70-9