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1-bromobutane-2,3-dione 3-oxime is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

2840-10-0

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2840-10-0 Usage

Functional Group

2,3-dione 3-oxime

Derivative of

1-bromobutane

Usage

Organic synthesis and chemical reactions

Reactivity

Likely to be reactive

Health Risks

a. Skin irritation
b. Respiratory irritation
c. Potential toxicity

Handling Precautions

Exercise caution in laboratory and industrial settings

Potential Hazards

Chemical compound with hazardous properties

Check Digit Verification of cas no

The CAS Registry Mumber 2840-10-0 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 2,8,4 and 0 respectively; the second part has 2 digits, 1 and 0 respectively.
Calculate Digit Verification of CAS Registry Number 2840-10:
(6*2)+(5*8)+(4*4)+(3*0)+(2*1)+(1*0)=70
70 % 10 = 0
So 2840-10-0 is a valid CAS Registry Number.
InChI:InChI=1/C4H6BrNO2/c1-3(6-8)4(7)2-5/h8H,2H2,1H3/b6-3-

2840-10-0SDS

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 1-bromobutane-2,3-dione-3-oxime

1.2 Other means of identification

Product number -
Other names 1-Brom-3-hydroxyimino-butan-2-on

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:2840-10-0 SDS

2840-10-0Relevant academic research and scientific papers

Stereoselectivity in the formation of tris-diimine complexes of Fe(ii), Ru(ii), and Os(ii) with a C2-symmetric chiral derivative of 2,2′-bipyridine

Drahonovsky, Dusan,Knof, Ulrich,Jungo, Laurence,Belser, Thomas,Neels, Antonia,Labat, Gael Charles,Stoeckli-Evans, Helen,Von Zelewsky, Alex

, p. 1444 - 1454 (2006)

A C2-symmetric enantiopure 4,5-bis(pinene)-2, 2′-bipyridine ligand (-)-L was used to investigate the diastereoselectivity in the formation of [ML3]2+ coordination species (M = Fe(ii), Ru(ii), Os(ii), Zn(ii), Cd(ii), Cu(ii), Ni(ii)), and [ML2Cl2] (M = Ru(ii), Os(ii)). The X-ray structures of the [ML3]2+ complexes were determined for Δ-[FeL3](PF6)2, Δ-[RuL 3](PF6)2, Λ-[RuL3](PF 6)2, Δ-[OsL3](PF6) 2, and Λ-[OsL3](TfO)2. All of these compounds were also characterized by NMR, CD and UV/VIS absorption spectroscopy. The [FeL3]2+ diastereoisomers were studied in equilibrated solutions at various temperatures and in several solvents. The [RuL3]2+ complexes, which are thermally stable up to 200 °C, were photochemically equilibrated. The Royal Society of Chemistry 2006.

A C3-symmetric chiral hexadentate podand ligand based on a tris(pyrazolyl)borate core

Motson,Mamula,Jeffery,McCleverty,Ward,Von Zelewsky

, p. 1389 - 1391 (2001)

A hexadentate podand ligand having C3 symmetry has been prepared, consisting of a tris(pyrazolyl)borate core bearing pinene-functionalised 2-pyridyl units attached to the C3 position of each pyrazolyl ring such that each arm is a chiral bidentate chelate; complexes with Tl(I) and Tb(III) have been prepared and structurally characterised.

5-(3-Bromophenyl)-7-(6-morpholin-4-ylpyridin-3-yl)pyrido[2,3-d] pyrimidin-4-ylamine: Structure-activity relationships of 7-substituted heteroaryl analogs as non-nucleoside adenosine kinase inhibitors

Matulenko, Mark A.,Lee, Chih-Hung,Jiang, Meiqun,Frey, Robin R.,Cowart, Marlon D.,Bayburt, Erol K.,DiDomenico Jr., Stanley,Gfesser, Gregory A.,Gomtsyan, Arthur,Guo, Zhu Zheng,McKie, Jeffery A.,Stewart, Andrew O.,Yu, Haixia,Kohlhaas, Kathy L.,Alexander, Karen M.,McGaraughty, Steve,Wismer, Carol T.,Mikusa, Joseph,Marsh, Kennan C.,Snyder, Ronald D.,Diehl, Marilyn S.,Kowaluk, Elizabeth A.,Jarvis, Michael F.,Bhagwat, Shripad S.

, p. 3705 - 3720 (2007/10/03)

4-Amino-5,7-disubstituted pyridopyrimidines are potent, non-nucleoside inhibitors of adenosine kinase (AK). We recently identified a potent, orally efficacious analog, 4 containing a 7-pyridylmorpholine substituted ring system as the key structural element of this template. In this report, we disclose the pharmacologic effects of five- and six-membered heterocyclic ring replacements for the pyridine ring in 4. These replacements were found to have interesting effects on in vivo efficacy and genotoxicity as well as in vitro potency. We discovered that the nitrogen in the heterocyclic ring at C(7) is important for the modulation of mutagenic side effects (Ames assay).

Platinum(II) compounds with enantiomerically pure bis(pinene)-fused bipyridine ligands - Diimine-dichloro complexes and their substitution reactions

Kolp, Brunhilde,Abeln, Dirk,Stoeckli-Evans, Helen,Von Zelewsky, Alexander

, p. 1207 - 1220 (2007/10/03)

The synthesis of chiral square-planar PtII complexes using symmetrical and unsymmetrical bis(pinene)-fused 2,2′-bipyridine is described. The neutral diimine dichloro complexes show a strong deviation of the coordination sphere from planarity if the pinene groups are attached at the 5-and 6-positions of the pyridine rings. However, this distortion does not occur in parallel with the chiral configuration at the diimine ligands. The substitution of the two cis-chloro ligands with diamines to form five-membered chelate rings shows little diastereoselectivity when racemic mixtures of chiral diamines are used. Also, ligands that are prochiral at the ligating centers show little selectivity upon coordination.

Kinetics of the Enolisation Reactions of 2-Acetylpyrrole and of 2-, 4- and 5-Acetylthiazoles

Maria, Paolo De,Fontana, Antonella,Arlotta, Marialuisa,Chimichi, Stefano,Spinelli, Domenico

, p. 415 - 420 (2007/10/02)

Kinetic results are reported on the rates of enolisation of title compounds in water, in acetate buffers, in dilute hydrochloric acid, in dilute sodium hydroxide solutions and in the presence of several metal-ion salts, as measured by their rates of halogenation at 25 deg C.The results have been compared with those previously obtained from the corresponding reactions of acetophenone and a number of acetylheterocycles.It is shown that a suitable metal cation (e.g., Cu2+) can be hundreds of times more effective than the proton in catalysing the enolisation process of an acetylheterocyclic compound.This can be due either to the 'soft' character of the acetyl group, as, for example, that of 2-acetylpyrrole, or to coordination of both the carbonyl oxygen and the heteroatom by the metal cation in the transition state of the reaction, as for 2- and 4-acetylthiazoles.

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