ChemicalBook >> CAS DataBase List >>2,4-Dichloro-5-thiazolecarboxaldehyde

2,4-Dichloro-5-thiazolecarboxaldehyde

CAS No.
92972-48-0
Chemical Name:
2,4-Dichloro-5-thiazolecarboxaldehyde
Synonyms
e-5-carbaL;oro-1,3-thiazoL;BUTTPARK 121\04-87;IFLAB-BB F2124-0686;2,4-DICHLORO-5-FORMYLTHIAZOLE;2,4-Dichloro-5-formyl-1,3-thiazole;2,4-DICHLOROTHIAZOLE-5-CARBALDEHYDE;2,4-Dichloro-thiazol-5-carbaldehyde;2,4-DICHLOROTHIAZOL-5-CARBOXALDEHYDE;2,4-DICHLORO-5-THIAZOLECARBOXALDEHYDE
CBNumber:
CB3328000
Molecular Formula:
C4HCl2NOS
Molecular Weight:
182.03
MDL Number:
MFCD00793013
MOL File:
92972-48-0.mol
MSDS File:
SDS
TDS File:
TDS
Last updated:2026-04-24 14:56:55
Product description Number Pack Size Price
2,4-Dichlorothiazole-5-carboxaldehyde 97% 724300 1g $75.7
2,4-DICHLORO-5-FORMYLTHIAZOLE 95% 22518 1G $33
2,4-DICHLORO-5-FORMYLTHIAZOLE 95% 22518 5G $77
2,4-Dichloro-5-thiazolecarboxaldehyde D435925 250mg $50
2,4-Dichloro-5-thiazolecarboxaldehyde D435925 1g $90
More product size

2,4-Dichloro-5-thiazolecarboxaldehyde Properties

Melting point 47-53℃
Boiling point 307.1±45.0 °C(Predicted)
Density 1.690±0.06 g/cm3(Predicted)
Flash point >110°C
storage temp. under inert gas (nitrogen or Argon) at 2-8°C
solubility DMSO (Slightly), Methanol (Slightly)
form Solid
pka -3.71±0.10(Predicted)
color Pale Beige
InChI 1S/C4HCl2NOS/c5-3-2(1-8)9-4(6)7-3/h1H
InChIKey CFEKBKCGPASOFI-UHFFFAOYSA-N
SMILES Clc1nc(Cl)c(C=O)s1
CAS DataBase Reference 92972-48-0(CAS DataBase Reference)
UNSPSC Code 12352100
NACRES NA.22

SAFETY

Risk and Safety Statements

Symbol(GHS)  GHS hazard pictograms
GHS06
Signal word  Danger
Hazard statements  H301-H319
Precautionary statements  P301+P310+P330-P305+P351+P338
Hazard Codes  Xi,Xn
Risk Statements  36/37/38-36-22
Safety Statements  26-36/37/39
RIDADR  UN 2811 6.1/PG 3
WGK Germany  3
Hazard Note  Irritant
HazardClass  6.1
HS Code  29341000
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
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
2 0

2,4-Dichloro-5-thiazolecarboxaldehyde price More Price(38)

Manufacturer Product number Product description CAS number Packaging Price Updated Buy
Sigma-Aldrich 724300 2,4-Dichlorothiazole-5-carboxaldehyde 97% 92972-48-0 1g $75.7 2023-06-20 Buy
AstaTech 22518 2,4-DICHLORO-5-FORMYLTHIAZOLE 95% 92972-48-0 1G $33 2026-04-30 Buy
AstaTech 22518 2,4-DICHLORO-5-FORMYLTHIAZOLE 95% 92972-48-0 5G $77 2026-04-30 Buy
TRC D435925 2,4-Dichloro-5-thiazolecarboxaldehyde 92972-48-0 250mg $50 2021-12-16 Buy
TRC D435925 2,4-Dichloro-5-thiazolecarboxaldehyde 92972-48-0 1g $90 2021-12-16 Buy
Product number Packaging Price Buy
724300 1g $75.7 Buy
22518 1G $33 Buy
22518 5G $77 Buy
D435925 250mg $50 Buy
D435925 1g $90 Buy

2,4-Dichloro-5-thiazolecarboxaldehyde Chemical Properties,Uses,Production

Uses

2,4-Dichloro-5-thiazolecarboxaldehyde is used in the synthesis of some novel thiazolidine-2,4-dione derivatives having antimicrobial activity.

Synthesis

2,4-Thiazolidinedione

2295-31-0

N,N-Dimethylformamide

68-12-2

2,4-Dichloro-5-thiazolecarboxaldehyde

92972-48-0

General procedure for the synthesis of 2,4-dichlorothiazole-5-carboxaldehyde (330): 2,4-thiazolidinedione (329, 2.7 g, 23.07 mmol) was dissolved in N,N-dimethylformamide (DMF, 1.23 mL, 15.98 mmol) at 0 °C and protected by argon and slowly added dropwise to phosphorus trichloride (8.15 mL, 87.17 mmol) (8.15 mL, 87.17 mmol), and the dropwise addition time was controlled at 15 min. Subsequently, the reaction mixture was gradually warmed to room temperature and stirred continuously for 1 hour. Next, the reaction system was heated to 120 °C and stirring was continued for 4 hours. The reaction process was monitored by thin layer chromatography (TLC). Upon completion of the reaction, the reaction mixture was carefully poured into pre-cooled ice water and extracted with dichloromethane (CH2Cl2, 3 x 100 mL). The organic phases were combined, washed sequentially with saturated sodium bicarbonate solution (100 mL) and water (100 mL), dried over anhydrous sodium sulfate, filtered and concentrated under reduced pressure to give the crude product. The crude product was purified by silica gel column chromatography with 5% ethyl acetate/hexane as eluent, and the target compound 330 (1.4 g, 33% yield) was finally obtained as a brown oil.TLC conditions: 30% ethyl acetate/hexane (Rf=0.8).1H NMR (500 MHz, DMSO-d6): δ9.87 (s, 1H).

References

[1] Journal of the Chemical Society, Perkin Transactions 1: Organic and Bio-Organic Chemistry (1972-1999), 1992, # 8, p. 973 - 978
[2] Bioorganic and Medicinal Chemistry Letters, 2004, vol. 14, # 1, p. 235 - 238
[3] Phosphorus, Sulfur and Silicon and the Related Elements, 2006, vol. 181, # 10, p. 2435 - 2444
[4] Patent: US2010/298334, 2010, A1. Location in patent: Page/Page column 78
[5] Chemistry of Heterocyclic Compounds, 2010, vol. 46, # 3, p. 334 - 341

2295-31-0
92972-48-0
Synthesis of 2,4-Dichloro-5-thiazolecarboxaldehyde from 2,4-Thiazolidinedione

2,4-Dichloro-5-thiazolecarboxaldehyde Preparation Products And Raw materials

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View Lastest Price from 2,4-Dichloro-5-thiazolecarboxaldehyde manufacturers

Image Update time Product Price Min. Order Purity Supply Ability Manufacturer
2,4-Dichloro-5-thiazolecarboxaldehyde pictures 2019-07-06 2,4-Dichloro-5-thiazolecarboxaldehyde
92972-48-0
US $1.00 / KG 1KG 95% 500KG Career Henan Chemical Co

2,4-Dichloro-5-thiazolecarboxaldehyde Spectrum

BUTTPARK 121\04-87 IFLAB-BB F2124-0686 2,4-DICHLORO-5-THIAZOLECARBOXALDEHYDE 2,4-DICHLORO-5-FORMYLTHIAZOLE 2,4-DICHLOROTHIAZOLE-5-CARBALDEHYDE 2,4-DICHLOROTHIAZOLE-5-CARBOXALDEHYDE 2,4-DICHLOROTHIAZOL-5-CARBOXALDEHYDE 2,4-DICHLORO-1,3-THIAZOLE-5-CARBALDEHYDE 2,4-Dichloro-1,3-thiazole-5-carboxaldehyde 2,4-Dichloro-5-formyl-1,3-thiazole 5-Thiazolecarboxaldehyde, 2,4-dichloro- 2,4-Dichlorothiazole-5-carboxaldehyde 97% 2,4-Dichloro-1,3-thiazole-5-carboxaldehyde 98% e-5-carbaL oro-1,3-thiazoL 2,4-Dichloro-thiazol-5-carbaldehyde 2,4-Dichloro-5-thiazolecarboxaldehyde 97% 92972-48-0 92973-48-0 92972-48-2 2972-48-0 C4HCl2NOS ALDEHYDE Aldehydes Building Blocks C1 to C6 Carbonyl Compounds Chemical Synthesis Halogenated Heterocycles Heterocyclic Building Blocks Organic Building Blocks Thiazoles Heterocycles Intermediates & Fine Chemicals Pharmaceuticals Sulfur & Selenium Compounds Aldehyde Organohalides Thiazole API intermediates