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6193-47-1

6193-47-1

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6193-47-1 Usage

Chemical Properties

CLEAR YELLOW LIQUID

Check Digit Verification of cas no

The CAS Registry Mumber 6193-47-1 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 6,1,9 and 3 respectively; the second part has 2 digits, 4 and 7 respectively.
Calculate Digit Verification of CAS Registry Number 6193-47:
(6*6)+(5*1)+(4*9)+(3*3)+(2*4)+(1*7)=101
101 % 10 = 1
So 6193-47-1 is a valid CAS Registry Number.
InChI:InChI=1/C8H8OS/c9-8(6-3-4-6)7-2-1-5-10-7/h1-2,5-6H,3-4H2

6193-47-1 Well-known Company Product Price

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  • (Code)Product description
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  • Aldrich

  • (C121207)  Cyclopropyl2-thienylketone  97%

  • 6193-47-1

  • C121207-5G

  • 583.83CNY

  • Detail

6193-47-1SDS

SAFETY DATA SHEETS

According to Globally Harmonized System of Classification and Labelling of Chemicals (GHS) - Sixth revised edition

Version: 1.0

Creation Date: Aug 12, 2017

Revision Date: Aug 12, 2017

1.Identification

1.1 GHS Product identifier

Product name Cyclopropyl 2-Thienyl Ketone

1.2 Other means of identification

Product number -
Other names cyclopropyl(thiophen-2-yl)methanone

1.3 Recommended use of the chemical and restrictions on use

Identified uses For industry use only.
Uses advised against no data available

1.4 Supplier's details

1.5 Emergency phone number

Emergency phone number -
Service hours Monday to Friday, 9am-5pm (Standard time zone: UTC/GMT +8 hours).

More Details:6193-47-1 SDS

6193-47-1Relevant articles and documents

Palladium-Catalyzed Carbonylative Cross-Coupling Reaction between Aryl(Heteroaryl) Iodides and Tricyclopropylbismuth: Expedient Access to Aryl Cyclopropylketones

Benoit, Emeline,Dansereau, Julien,Gagnon, Alexandre

supporting information, p. 2833 - 2838 (2017/10/06)

The carbonylative cross-coupling reaction between aryl and heteroaryl iodides and tricyclopropylbismuth is reported. The reaction is catalyzed by (SIPr)Pd(allyl)Cl, a NHC-palladium(II) catalyst, operates under 1 atm of carbon monoxide and tolerates a wide range of functional groups. The use of lithium chloride was found to provide higher yields of the desired aryl cyclopropylketones. The conditions were also applied to the carbonylative cross-coupling of an iodoalkene to afford the corresponding alkenyl cyclopropylketone.

Substituted Geminal Dithienyltetrahydrofurans via an Intramolecular Williamson Reaction

Sonnewald, Ursula

, p. 567 - 568 (2007/10/02)

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