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2-Chloro-5-iodothiophene

CAS No.
28712-49-4
Chemical Name:
2-Chloro-5-iodothiophene
Synonyms
2-Chloro-5-iodothiophene;Thiophene, 2-chloro-5-iodo-
CBNumber:
CB22487528
Molecular Formula:
C4H2ClIS
Molecular Weight:
244.48
MDL Number:
MFCD18382465
MOL File:
28712-49-4.mol
MSDS File:
SDS
Last updated:2025-07-24 18:13:46
Product description Number Pack Size Price
2-Chloro-5-iodothiophene 096648 250.00mg $545
2-Chloro-5-iodothiophene 096648 1.00g $1210
2-CHLORO-5-IODOTHIOPHENE 95.00% HCH0363552 5MG $496.11
2-Chloro-5-iodothiophene 95+% 096648 250mg $545
2-Chloro-5-iodothiophene 95+% 096648 1g $1210

2-Chloro-5-iodothiophene Properties

Melting point -25--24 °C
Boiling point 95-96 °C(Press: 14 Torr)
Density 2.164±0.06 g/cm3(Predicted)
storage temp. under inert gas (nitrogen or Argon) at 2–8 °C

2-Chloro-5-iodothiophene price More Price(18)

Manufacturer Product number Product description CAS number Packaging Price Updated Buy
Matrix Scientific 096648 2-Chloro-5-iodothiophene 28712-49-4 250.00mg $545 2026-05-18 Buy
Matrix Scientific 096648 2-Chloro-5-iodothiophene 28712-49-4 1.00g $1210 2026-05-18 Buy
American Custom Chemicals Corporation HCH0363552 2-CHLORO-5-IODOTHIOPHENE 95.00% 28712-49-4 5MG $496.11 2021-12-16 Buy
Matrix Scientific 096648 2-Chloro-5-iodothiophene 95+% 28712-49-4 250mg $545 2021-12-16 Buy
Matrix Scientific 096648 2-Chloro-5-iodothiophene 95+% 28712-49-4 1g $1210 2021-12-16 Buy
Product number Packaging Price Buy
096648 250.00mg $545 Buy
096648 1.00g $1210 Buy
HCH0363552 5MG $496.11 Buy
096648 250mg $545 Buy
096648 1g $1210 Buy

2-Chloro-5-iodothiophene Chemical Properties,Uses,Production

Synthesis

2-Iodothiophene

3437-95-4

2-Chloro-5-iodothiophene

28712-49-4

The general procedure for the synthesis of 2-chloro-5-iodothiophene from 2-iodothiophene is as follows: Example 1: Synthesis of 1-(5-chlorothiophen-2-yl)-2-(2,4-difluorophenyl)-1,1-difluoro-3-(1H-tetrazol-1-yl)propan-2-ol 1. 2-Iodothiophene (2.5 g, 11.9 mmol) was dissolved in hexane (25 mL) and stirred until completely dissolved. 2. N-chlorosuccinimide (NCS; 1.58 g, 11.9 mmol) was added to the above solution. 3. A catalytic amount of perchloric acid (HClO4) was added and the reaction was stirred continuously for 24 hours (h) at room temperature (RT). 4. Upon completion of the reaction, the reaction mixture was filtered and the filtrate was collected. 5. The filtrate was washed sequentially with water (H2O) and brine and then dried with anhydrous sodium sulfate (Na2SO4). 6. The dried filtrate was concentrated under vacuum to give 2-chloro-5-iodothiophene in liquid form (1.7 g, 6.9 mmol, 58% yield). Product characterization: 1H NMR (200 MHz, CDCl3): δ 7.18 (d, J = 4.2 Hz, 1H), 6.69 (d, J = 4.2 Hz, 1H).

References

[1] Journal of Organic Chemistry, 1993, vol. 58, # 11, p. 3072 - 3075
[2] Patent: US2012/329802, 2012, A1. Location in patent: Page/Page column 18-19

96-43-5
28712-49-4
Synthesis of 2-Chloro-5-iodothiophene from 2-Chlorothiophene

2-Chloro-5-iodothiophene Preparation Products And Raw materials

2-Chloro-5-iodothiophene Suppliers

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28712-49-4(2-Chloro-5-iodothiophene)Related Search:

2-Chloro-5-iodothiophene Thiophene, 2-chloro-5-iodo- 28712-49-4 C4H2ClIS