Welcome to LookChem.com Sign In|Join Free

CAS

  • or

51445-63-7

Post Buying Request

51445-63-7 Suppliers

Recommended suppliersmore

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

51445-63-7 Usage

General Description

2-Thienylglyoxal is compound with the chemical formula C6H4O2S, consisting of a thiophene ring attached to a glyoxal structure. It is a heterocyclic aromatic compound that is used in the synthesis of various pharmaceuticals and organic compounds. It is also known for its potential applications as a fluorescent probe for detecting different metal ions due to its high affinity for metal chelation. Additionally, 2-Thienylglyoxal has been studied for its potential anti-inflammatory and antioxidant properties, making it a subject of interest in the field of medicinal chemistry. Overall, this compound has diverse uses and applications in the fields of organic chemistry, pharmaceuticals, and biomedical research.

Check Digit Verification of cas no

The CAS Registry Mumber 51445-63-7 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 5,1,4,4 and 5 respectively; the second part has 2 digits, 6 and 3 respectively.
Calculate Digit Verification of CAS Registry Number 51445-63:
(7*5)+(6*1)+(5*4)+(4*4)+(3*5)+(2*6)+(1*3)=107
107 % 10 = 7
So 51445-63-7 is a valid CAS Registry Number.
InChI:InChI=1/C6H4O2S/c7-4-5(8)6-2-1-3-9-6/h1-4H

51445-63-7SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 14, 2017

Revision Date: Aug 14, 2017

1.Identification

1.1 GHS Product identifier

Product name 2-Thienylglyoxal hydrate

1.2 Other means of identification

Product number -
Other names 2-thienyl-glyoxal

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:51445-63-7 SDS

51445-63-7Relevant articles and documents

-

Kipnis,Ornfelt

, p. 2734 (1946)

-

A novel class for carbonic anhydrases inhibitors and evaluation of their non-zinc binding

Kuzu, Burak,Tan, Meltem,Gül?in, ?lhami,Menges, Nurettin

, (2021/06/09)

In this study, 23 different imidazole derivatives were synthesized, and the inhibitory properties of these derivatives against carbonic anhydrase I and II isoenzymes were investigated for the first time. The inhibition concentrations of the imidazole derivatives were found to be in the range of 2.89–115.5 nM. Docking studies examined the binding properties of the imidazole derivatives, and the structure–activity relationship is discussed. Theoretical calculations showed that the binding mode of the imidazole ring was non-zinc binding.

Catalytic Asymmetric Darzens-Type Epoxidation of Diazoesters: Highly Enantioselective Synthesis of Trisubstituted Epoxides

Nam, Dong Guk,Shim, Su Yong,Jeong, Hye-Min,Ryu, Do Hyun

supporting information, p. 22236 - 22240 (2021/09/13)

Highly enantioselective Darzens-type epoxidation of diazoesters with glyoxal derivatives was accomplished using a chiral boron–Lewis acid catalyst, which facilitated asymmetric synthesis of trisubstituted α,β-epoxy esters. In the presence of a chiral oxazaborolidinium ion catalyst, the reaction proceeded in high yield (up to 99 %) with excellent enantio- and diastereoselectivity (up to >99 % ee and >20:1 dr, respectively). The synthetic potential of this method was illustrated by conversion of the products to various compounds such as epoxy γ-butyrolactone, tertiary β-hydroxy ketone and epoxy diester.

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 51445-63-7