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5-Bromothiophene-2-carboxaldehyde oxime is a chemical compound with a molecular formula of C5H4BrNOS. It belongs to the group of organobromine compounds, which are organic compounds that contain carbons linked to bromine atoms. This substance also falls under the category of oximes, compounds that feature a carbon-nitrogen double bond with another oxygen atom connected to the nitrogen. It is typically used in scientific research, particularly in the synthesis of more complex chemical compounds. Due to its chemical properties, it is important to handle this substance with caution as its health effects are not fully known.

2160-63-6

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2160-63-6 Usage

Uses

Used in Scientific Research:
5-Bromothiophene-2-carboxaldehyde oxime is used as a chemical intermediate for the synthesis of more complex chemical compounds. Its unique structure and reactivity make it a valuable component in the development of new molecules with potential applications in various fields.
Used in Organic Chemistry:
In the field of organic chemistry, 5-Bromothiophene-2-carboxaldehyde oxime is used as a reagent in various chemical reactions. Its organobromine and oxime functionalities allow for a range of reactions, such as coupling and condensation, which can lead to the formation of new compounds with desired properties.
Used in Pharmaceutical Development:
5-Bromothiophene-2-carboxaldehyde oxime may be used as a building block in the design and synthesis of new pharmaceutical compounds. Its unique structure could potentially contribute to the development of novel drugs with improved efficacy and reduced side effects.
Used in Material Science:
In material science, 5-Bromothiophene-2-carboxaldehyde oxime could be used in the synthesis of new materials with specific properties, such as improved conductivity, stability, or reactivity. Its incorporation into polymers or other materials could lead to the development of advanced materials for various applications.
Used in Environmental Applications:
5-Bromothiophene-2-carboxaldehyde oxime may also find use in environmental applications, such as in the development of new methods for pollution control or remediation. Its chemical properties could potentially be harnessed to improve the efficiency of environmental processes or to create new materials for environmental protection.

Check Digit Verification of cas no

The CAS Registry Mumber 2160-63-6 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 2,1,6 and 0 respectively; the second part has 2 digits, 6 and 3 respectively.
Calculate Digit Verification of CAS Registry Number 2160-63:
(6*2)+(5*1)+(4*6)+(3*0)+(2*6)+(1*3)=56
56 % 10 = 6
So 2160-63-6 is a valid CAS Registry Number.
InChI:InChI=1/C5H4BrNOS/c6-5-2-1-4(9-5)3-7-8/h1-3,8H/b7-3-

2160-63-6 Well-known Company Product Price

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  • Alfa Aesar

  • (B24968)  5-Bromothiophene-2-carboxaldoxime, 97%   

  • 2160-63-6

  • 1g

  • 368.0CNY

  • Detail
  • Alfa Aesar

  • (B24968)  5-Bromothiophene-2-carboxaldoxime, 97%   

  • 2160-63-6

  • 5g

  • 1476.0CNY

  • Detail

2160-63-6SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 16, 2017

Revision Date: Aug 16, 2017

1.Identification

1.1 GHS Product identifier

Product name 5-BROMOTHIOPHENE-2-CARBOXALDEHYDE OXIME

1.2 Other means of identification

Product number -
Other names 5-Bromothiophene-2-carboxaldoxime

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:2160-63-6 SDS

2160-63-6Relevant academic research and scientific papers

Design, synthesis and in vitro activity of phidianidine B derivatives as novel PTP1B inhibitors with specific selectivity

Zhang, Li,Jiang, Cheng-Shi,Gao, Li-Xin,Gong, Jing-Xu,Wang, Zhong-Hua,Li, Jing-Ya,Li, Jia,Li, Xu-Wen,Guo, Yue-Wei

supporting information, p. 778 - 781 (2016/05/24)

A series of phidianidine B derivatives were synthesized by introducing various heterocyclic rings. Their inhibitory effects on PTP1B and other PTPs (TCPTP, SHP1, SHP2 and LAR) were evaluated. A majority of them displayed significant inhibitory potency and specific selectivity over PTP1B. The SAR and molecular docking analysis were also described.

Design of α7 nicotinic acetylcholine receptor ligands in quinuclidine, tropane and quinazoline series. Chemistry, molecular modeling, radiochemistry, in vitro and in rats evaluations of a [18F] quinuclidine derivative

Pin, Frédéric,Vercouillie, Johnny,Ouach, Aziz,Mavel, Sylvie,Gulhan, Zuhal,Chicheri, Gabrielle,Jarry, Christian,Massip, Stephane,Deloye, Jean-Bernard,Guilloteau, Denis,Suzenet, Franck,Chalon, Sylvie,Routier, Sylvain

, p. 214 - 224 (2014/06/24)

In this report, we describe the synthesis of a novel library of α7 nAChR ligands based on the modulation of the quinuclidine, quinazoline and tropane moieties. Spirane derivatives were newly synthesized under stereo specific 1,3 dipolar cylcoadditions. On

A practical and cost-efficient, one-pot conversion of aldehydes into nitriles mediated by 'activated DMSO'

Augustine, John Kallikat,Bombrun, Agnes,Atta, Rajendra Nath

experimental part, p. 2223 - 2227 (2011/10/31)

Participation of activated DMSO in the one-pot transformation of aldehydes to nitriles has been described by reacting aldehydes with NHHHCl in DMSO in the absence of any added base or catalyst. The method is applicable to access a wide range of aromatic, heterocyclic, and aliphatic nitriles, in which only water is a byproduct. A straightforward and practical procedure is demonstrated on a multigram scale. Georg Thieme Verlag Stuttgart - New York.

NOVEL ANTIMALARIA AGENT CONTAINING HETEROCYCLIC COMPOUND

-

Page/Page column 51, (2008/06/13)

Disclosed is an antimalarial agent containing a compound represented by the formula: [wherein A1 represents a 3-pyridyl group that may have a substituent, a 6-quinolyl group that may have a substituent, or the like; X1 represents a group represented by the formula -C(=O)-NH- or the like; E represents a furyl group, a thienyl group or a phenyl group; with the proviso that A1 may have one to three substituents, and E has one of two substituents] or a salt thereof or hydrates thereof.

OXAZOLIDINONE DERIVATIVES AS ANTIMICROBIALS

-

Page/Page column 29, (2010/02/13)

The present invention relates to certain substituted phenyl oxazolidinones of formula (I) and to processes for the synthesis of the same. This invention also relates to pharmaceutical compositions containing such compounds as antimicrobials. The compounds are useful antimicrobial agents, effective against a number of human and veterinary pathogens, including gram-positive aerobic bacteria such as multiple-resistant staphylococci, streptococci and enterococci as well as anaerobic organisms such as Bacterioides spp. and Clostridia spp. species, and acid-fast organisms such as Mycobacterium tuberculosis, Mycobacterium avium and Mycobacterium spp.

THIENYL COMPOUNDS

-

Page/Page column 17, (2008/06/13)

Compounds of formula I : and pharmaceutically-acceptable salts thereof, wherein Ar and R are as defined in the specification, compositions containing such compounds and the use of such compounds and compositions for use in therapy.

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