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BENZO[B]THIOPHENE-3-CARBONITRILE

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Products Intro: Product Name:BENZO[B]THIOPHENE-3-CARBONITRILE
CAS:24434-84-2
Purity:0.98 Package:based on the requirments Remarks:H
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Products Intro: Product Name:Benzo[b]thiophene-3-carbonitrile
CAS:24434-84-2
Purity:97+% Package:1g;10g;100g;;1kg Remarks:Z-55774
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Products Intro: Product Name:BENZO[B]THIOPHENE-3-CARBONITRILE
CAS:24434-84-2
Purity:95.0%-99.0% Package:1ASSAYS;6.05USD
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Products Intro: Product Name:1-benzothiophene-3-carbonitrile
CAS:24434-84-2
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Products Intro: Product Name:BENZO[B]THIOPHENE-3-CARBONITRILE
CAS:24434-84-2
Purity:99.00% Package:1g;1.1USD Remarks:ISO 9001:2015 REACH Approved Manufacturer

BENZO[B]THIOPHENE-3-CARBONITRILE manufacturers

BENZO[B]THIOPHENE-3-CARBONITRILE Basic information
Product Name:BENZO[B]THIOPHENE-3-CARBONITRILE
Synonyms:BENZO[B]THIOPHENE-3-CARBONITRILE;BUTTPARK 147\16-61;3-CYANOBENZO[B]THIOPHENE;Benzothiophene-3-carbonitrile;1-BENZOTHIOPHENE-3-CARBONITRILE;3-Cyano-1-benzothiophene;Benzo(b)thiophene-3-carbonitrile ,97%;Benzothiophene-3-nitrile
CAS:24434-84-2
MF:C9H5NS
MW:159.21
EINECS:
Product Categories:Benzothiophenes;Building Blocks;Chemical Synthesis;Heterocyclic Building Blocks
Mol File:24434-84-2.mol
BENZO[B]THIOPHENE-3-CARBONITRILE Structure
BENZO[B]THIOPHENE-3-CARBONITRILE Chemical Properties
Melting point 71-75 °C
Boiling point 312.7±15.0 °C(Predicted)
density 1.28±0.1 g/cm3(Predicted)
storage temp. Keep in dark place,Sealed in dry,Room Temperature
AppearanceWhite to light yellow Solid
Safety Information
Hazard Codes Xn
Risk Statements 22-36/37/38
Safety Statements 26
WGK Germany 3
HS Code 29349990
MSDS Information
BENZO[B]THIOPHENE-3-CARBONITRILE Usage And Synthesis
Chemical PropertiesWhite to light brown solid
Synthesis
1-Benzothiophene-3-carbaldehyde

5381-20-4

BENZO[B]THIOPHENE-3-CARBONITRILE

24434-84-2

General procedure for the synthesis of benzo[b]thiophene-3-carbonitrile from 3-formylbenzothiophene: To a premixed mixed solution of hexafluoroisopropanol (HFIP) and acetonitrile (ACN) (2.0 mL, 1:1) under nitrogen protection was added aromatic aldehyde 1 (0.500 mmol, 1.0 equiv.) and trimethylsilyl azide (TMSN3; 115 mg, 1.00 mmol, 2.0 equiv). Subsequently, trifluoromethanesulfonic acid (TfOH; 17.7 μL, 0.200 mmol, 0.40 eq.) was added to two dry vials, and exothermic and rapid foaming phenomena due to gas production were immediately observed. The vial was quickly capped and the reaction mixture was stirred at room temperature for 20 to 75 min. Upon completion of the reaction, the reaction mixture was concentrated under nitrogen atmosphere. The obtained residue was suspended in a solvent mixture of dichloromethane (CH2Cl2) and hexane and loaded through a sample cassette containing 5 g silica gel. Purification was carried out by normal-phase silica gel fast column chromatography using a CombiFlash purification system, and suitable elution fractions were collected and concentrated to give the target product benzo[b]thiophene-3-carbonitrile (2).

References[1] Molecules, 2016, vol. 21, # 1,
[2] Organic and Biomolecular Chemistry, 2016, vol. 14, # 5, p. 1840 - 1840
[3] Tetrahedron Letters, 2013, vol. 54, # 17, p. 2177 - 2179
[4] Organic and Biomolecular Chemistry, 2015, vol. 13, # 30, p. 8322 - 8329
BENZO[B]THIOPHENE-3-CARBONITRILE Preparation Products And Raw materials
Raw materials1-Benzothiophene-3-carbaldehyde-->3-Bromo-1-benzothiophene-->Sodium cyanide-->Azidotrimethylsilane
Tag:BENZO[B]THIOPHENE-3-CARBONITRILE(24434-84-2) Related Product Information
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