ChemicalBook > Product Catalog > Pharmaceutical intermediates > Heterocyclic compound > Thiophene compounds > 2-Iodothiophene
2-Iodothiophene
2-Iodothiophene Basic information
- Product Name:
- 2-Iodothiophene
- Synonyms:
-
- 2-Iodothiophene
- 2-Iodothiophene, 98+% 10ML
- 2-Iodothiophene, 98%, stab. with copper
- 2-IODTHIOPHENE
- 2-THIENYL IODIDE
- 2-iodo-thiophen
- 2-Iodothyophene
- alpha-Iodothiophene
- CAS:
- 3437-95-4
- MF:
- C4H3IS
- MW:
- 210.04
- EINECS:
- 222-342-1
- Product Categories:
-
- Thiophenes & Benzothiophenes
- Halogenated Heterocycles
- Heterocyclic Building Blocks
- ThiophenesBuilding Blocks
- Heterocycle-oher series
- alkyl Iodine
- Thiophenes
- Sulphur Derivatives
- Halides
- Thiophenes & Benzothiophenes
- Thiophene&Benzothiophene
- Mol File:
- 3437-95-4.mol
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2-Iodothiophene Chemical Properties
- Melting point:
- -40 °C (lit.)
- Boiling point:
- 73 °C/15 mmHg (lit.)
- Density
- 1.902 g/mL at 25 °C (lit.)
- refractive index
- n20/D 1.651(lit.)
- Flash point:
- 160 °F
- storage temp.
- 2-8°C
- form
- Liquid
- Specific Gravity
- 1.902
- color
- Clear yellow-green to red-brown
- Sensitive
- Light Sensitive
- BRN
- 104666
- InChIKey
- ROIMNSWDOJCBFR-UHFFFAOYSA-N
- CAS DataBase Reference
- 3437-95-4(CAS DataBase Reference)
- NIST Chemistry Reference
- Thiophene, 2-iodo-(3437-95-4)
- EPA Substance Registry System
- Thiophene, 2-iodo- (3437-95-4)
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Safety Information
- Hazard Codes
- Xn,Xi
- Risk Statements
- 22-37/38-41-43-20/21/22-36/37/38
- Safety Statements
- 26-36/37/39-36/37-27
- WGK Germany
- 3
- F
- 3
- TSCA
- T
- HazardClass
- IRRITANT
- HS Code
- 29349990
MSDS
- Language:English Provider:2-Iodothiophene
- Language:English Provider:ACROS
- Language:English Provider:SigmaAldrich
- Language:English Provider:ALFA
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2-Iodothiophene Usage And Synthesis
Chemical Properties
colorless to light yellow liquid
Uses
2-Iodothiophene was used in the synthesis of (E)-and (Z)-2,3-difluoro-3-aryl substituted acrylic esters. It was also used as monomer in the preparation of thin conductive films via plasma polymerization of 2-iodothiophene.
Synthesis Reference(s)
Tetrahedron Letters, 36, p. 4883, 1995 DOI: 10.1016/0040-4039(95)00876-E
General Description
Mechanism of the fluoride-free, palladium-catalyzed cross-coupling reaction of 2-iodothiophene with potassium (E)-heptenyldimethylsilanolate has been investigated. 2-Iodothiophene participates in microwave-enhanced, rapid homogeneous-phase version of the Sonogashira reaction.
2-Iodothiophene Preparation Products And Raw materials
Raw materials
Preparation Products
2-IodothiopheneSupplier
Sanjing New Materials Technology (Taizhou) Co., Ltd. Gold
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- 15250805028
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J & K SCIENTIFIC LTD.
- Tel
- 010-82848833 400-666-7788
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Meryer (Shanghai) Chemical Technology Co., Ltd.
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- 021-61259108 18621169109
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Beijing Donghualituo Techonlogy Development Co.,Ltd.
- Tel
- 010-88425576
- sales@dhltchem.com
INTATRADE GmbH
- Tel
- +49 3493/605464
- sales@intatrade.de
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2-Iodothiophene(3437-95-4)Related Product Information
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