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ChemicalBook >> CAS DataBase List >>2,3-Dichloroquinoxaline

2,3-Dichloroquinoxaline

CAS No.
2213-63-0
Chemical Name:
2,3-Dichloroquinoxaline
Synonyms
cp42103-4;NSC 33437;oroquinoxaL;AKOS BBS-00006726;TIMTEC-BB SBB003555;SALOR-INT L497169-1EA;3-Dichloroquinoxaline;2,3-DICHLOROQUINOXALINE;2,3-dichloro-quinoxalin;2,3-Dichlcroquinoxaline
CBNumber:
CB5414800
Molecular Formula:
C8H4Cl2N2
Molecular Weight:
199.04
MDL Number:
MFCD00006720
MOL File:
2213-63-0.mol
MSDS File:
SDS
TDS File:
TDS
Last updated:2026-05-28 03:48:40
Product description Number Pack Size Price
2,3-Dichloroquinoxaline 96% 144525 10g $65.7
2,3-Dichloroquinoxaline 96% 144525 50g $274
2,3-Dichloroquinoxaline >98.0%(GC) D2622 5g $34
2,3-Dichloroquinoxaline >98.0%(GC) D2622 25g $110
2,3-Dichloroquinoxaline Asreported 270793 5g $313
More product size

2,3-Dichloroquinoxaline Properties

Melting point 152-154 °C (lit.)
Boiling point 325.69°C (rough estimate)
Density 1.4994 (rough estimate)
refractive index 1.6400 (estimate)
storage temp. Keep in dark place,Sealed in dry,Room Temperature
Water Solubility Insoluble in water
solubility soluble in Chloroform
pka -4.78±0.48(Predicted)
form Needles
color Off-white to light brown
BRN 126076
Stability Stable. Incompatible with strong oxidizing agents.
InChI 1S/C8H4Cl2N2/c9-7-8(10)12-6-4-2-1-3-5(6)11-7/h1-4H
InChIKey SPSSDDOTEZKOOV-UHFFFAOYSA-N
SMILES Clc1nc2ccccc2nc1Cl
CAS DataBase Reference 2213-63-0(CAS DataBase Reference)
FDA UNII 3V2TXX4YAZ
EPA Substance Registry System 2,3-Dichloroquinoxaline (2213-63-0)
UNSPSC Code 12352100
NACRES NA.22

SAFETY

Risk and Safety Statements

Symbol(GHS)  Skull and Crossbones (GHS06)
GHS06
Signal word  Danger
Hazard statements  H301-H315-H319-H335
Precautionary statements  P301+P310+P330-P302+P352-P305+P351+P338
target organs Respiratory system
PPE Eyeshields, Faceshields, Gloves, type P2 (EN 143) respirator cartridges
Hazard Codes  T
Risk Statements  25-36/37/38
Safety Statements  26-36/37/39-45-37/39-28A
RIDADR  2811
WGK Germany  3
RTECS  VD1720000
TSCA  TSCA listed
HazardClass  6.1
PackingGroup  III
HS Code  29339900
Storage Class 6.1C - Combustible acute toxic Cat.3
toxic compounds or compounds which causing chronic effects
Hazard Classifications Acute Tox. 3 Oral
Eye Irrit. 2
Skin Irrit. 2
STOT SE 3
Toxicity mouse,LD50,intravenous,5600ug/kg (5.6mg/kg),U.S. Army Armament Research & Development Command, Chemical Systems Laboratory, NIOSH Exchange Chemicals. Vol. NX#03256,
Limited Quantities 5.0 L (1.3 gallons) (liquid) or 5.0 kg (11 lbs) (solid)
Excepted Quantities Max Inner Pack (30g or 30ml) and Max Outer Pack (1Kg or 1L)
NFPA 704
1
3 0

2,3-Dichloroquinoxaline price More Price(101)

Manufacturer Product number Product description CAS number Packaging Price Updated Buy
Sigma-Aldrich 144525 2,3-Dichloroquinoxaline 96% 2213-63-0 10g $65.7 2026-04-30 Buy
Sigma-Aldrich 144525 2,3-Dichloroquinoxaline 96% 2213-63-0 50g $274 2023-06-20 Buy
TCI Chemical D2622 2,3-Dichloroquinoxaline >98.0%(GC) 2213-63-0 5g $34 2026-04-30 Buy
TCI Chemical D2622 2,3-Dichloroquinoxaline >98.0%(GC) 2213-63-0 25g $110 2026-04-30 Buy
Usbiological 270793 2,3-Dichloroquinoxaline Asreported 2213-63-0 5g $313 2026-06-03 Buy
Product number Packaging Price Buy
144525 10g $65.7 Buy
144525 50g $274 Buy
D2622 5g $34 Buy
D2622 25g $110 Buy
270793 5g $313 Buy

2,3-Dichloroquinoxaline Chemical Properties,Uses,Production

Description

2,3-Dichloroquinoxaline (DCQX) can be used as a substrate for nucleophilic aromatic substitution (SNAr) reactions and is a versatile building block for the synthesis of many quinoxaline derivatives. 2,3-Dichloroquinoxaline reacts with 6-aminothiouracil in ethanol/TEA to form 6-amino-2-(3-chloroquinoxalin-2-ylthio)pyrimidin-4(3H)-one. It reacts with cholest-5-en-3-one semicarbazone/thiosemicarbazone to form steriodal cholest-5-en-3-oxazolo and thiazoloquinoxaline.

Chemical Properties

solid

Uses

2,3-Dichloroquinoxaline was used in the synthesis of mono and 2,3-disubstituted quinoxalines. It was used in solid phase synthesis of HPLC chiral stationary phase containing the N,N′-dialkyl-2,3-diaminoquinoxaline group as a linking structure.

Uses

2,3-Dichloroquinoxaline is a dichlorinated quinoxaline derivative with antimicrobial activity. 2,3-Dichloroquinoxaline is used in the preparation of quinoxaline derivatives of cancer chemopreventive a ctivity.

Preparation

To a stirred solution of quinoxaline-2,3(1H,4H)-dione (5.00 g, 1.0 equiv.), POCl3 was added (20 ml) and refluxed at 100 °C for 3h. After completion of the reaction, as indicated by TLC, the reaction mass was distilled under vaccum and quenched with ice cold water. Off white semi solid was formed and is filtered through buchner funnel under vaccum to yield the 2,3-dichloroquinoxaline in excellent yield.
Preparation of 2,3-Dichloroquinoxaline
Appearance: off white solid; Yield: 92% (5.64g); ESI-MS: (m/z) calcd. for C8H4Cl2N2: 197.98, found: 199.10 [M+H]+.

General Description

Gray solid. Insoluble in water.

Air & Water Reactions

Insoluble in water.

Reactivity Profile

A halogenated amine. Amines are chemical bases. They neutralize acids to form salts plus water. These acid-base reactions are exothermic. The amount of heat that is evolved per mole of amine in a neutralization is largely independent of the strength of the amine as a base. Amines may be incompatible with isocyanates, halogenated organics, peroxides, phenols (acidic), epoxides, anhydrides, and acid halides. Flammable gaseous hydrogen is generated by amines in combination with strong reducing agents, such as hydrides.

Fire Hazard

2,3-Dichloroquinoxaline is probably combustible.

Synthesis

2,3-DIHYDROXYQUINOXALINE

15804-19-0

2,3-Dichloroquinoxaline

2213-63-0

General procedure for the synthesis of 2,3-dichloroquinoxaline from 2,3-dihydroxyquinoxaline: a mixture of quinoxaline-2,3(1H,4H)-dione (1) [16] or compound 2 (40 mmol) with phosphoryl chloride (100 mmol) in N,N-dimethylformamide (20 mL) was stirred and reacted for 4 hr at 50 °C. Upon completion of the reaction, the reaction mixture was slowly poured into an ice/water mixture and neutralized with 30% ammonia solution. The resulting precipitate was collected by filtration and purified by column chromatography, the eluent being a solvent mixture of petroleum ether (60-80°C fraction) and ethyl acetate (9:1, v/v).

Purification Methods

Recrystallise it from *C6H6 and dry it in a vacuum [Cheeseman J Chem Soc 1804 1955, Beilstein 23/7 V 144].

References

[1] Tetrahedron, 2008, vol. 64, # 22, p. 5410 - 5415
[2] ChemMedChem, 2012, vol. 7, # 5, p. 823 - 835
[3] European Journal of Medicinal Chemistry, 2011, vol. 46, # 1, p. 327 - 340
[4] Indian Journal of Chemistry, Section B: Organic Chemistry Including Medicinal Chemistry, 1991, vol. 30, # 10, p. 936 - 940
[5] Helvetica Chimica Acta, 1994, vol. 77, # 6, p. 1549 - 1556

15804-19-0
2213-63-0
Synthesis of 2,3-Dichloroquinoxaline from 2,3-DIHYDROXYQUINOXALINE
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View Lastest Price from 2,3-Dichloroquinoxaline manufacturers

Image Update time Product Price Min. Order Purity Supply Ability Manufacturer
2, 3-Dichloroquinoxaline pictures 2026-05-28 2, 3-Dichloroquinoxaline
2213-63-0
$10.00 1KG 98% 10 ton Hebei Chuanghai Biotechnology Co,.LTD
2,3-Dichloroquinoxaline pictures 2026-03-20 2,3-Dichloroquinoxaline
2213-63-0
$1.00 1KG 99% 10 mt Hebei Chuanghai Biotechnology Co., Ltd
2,3-Dichloroquinoxaline pictures 2025-06-20 2,3-Dichloroquinoxaline
2213-63-0
1kg 99.00% 100tons Hebei Yanxi Chemical Co., Ltd.
2,3-dichloro-quinoxalin cp42103-4 AKOS BBS-00006726 2,3-DICHLOROQUINOXALINE SALOR-INT L497169-1EA TIMTEC-BB SBB003555 Quinoxaline, 2,3-dichloro. 2,3-Dichloroquinoxaline ,98% 2,3-Dichloroquinoxaline,97% NSC 33437 2,3-Dichloroquinoxaline,96% 3-Dichloroquinoxaline 2,3-Dichloroquinoxaline, 97% 10GR 2,3-dichloroquinoxazoline 2,3-Dichloroquinoxaline, 97.5% 2,3-dichloroquinoxaline2213-63-0 2,3-Dichlcroquinoxaline JR-8372, 2,3-Dichloroquinoxaline, 97% 2,3-Dichloroquinoxaline> oroquinoxaL 2213-63-0 2,3-Dichloroquinoxaline 6H-Benzo[cd]pyren-11-one 4-Hydroxybenzaldehyde,p-Hydroxybenzaldehyde,4-Hydroxybenzenecarbonal,Para Hydroxy Benzaldehyde,PHB,p-hydroxy-benzaldehyd,4-hydroxybenzaldehyde,p-Formylphenol,p-Oxybenzaldehyde,USAF m-6 2,3-Dichloroquinoxaline,2,3-Dichloro-quinoxaline,Quinoxaline,2,3-dichloro-,2,3-dichloroquinaxoline,2,3-dichloroquinoxazoline,NSC 2213-63-0 2212-63-0 Heterocyclic Building Blocks Halogenated Heterocycles Quinoxalines Building Blocks Building Blocks Halogenated Heterocycles Heterocyclic Building Blocks Quinoxalines QuinoxalinesHeterocyclic Building Blocks 1 2213-63-0
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