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2(5H)-Furanone, 5-methyl-5-(2-methylpropyl)- is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

110296-01-0

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110296-01-0 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 110296-01-0 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,1,0,2,9 and 6 respectively; the second part has 2 digits, 0 and 1 respectively.
Calculate Digit Verification of CAS Registry Number 110296-01:
(8*1)+(7*1)+(6*0)+(5*2)+(4*9)+(3*6)+(2*0)+(1*1)=80
80 % 10 = 0
So 110296-01-0 is a valid CAS Registry Number.

110296-01-0SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 15, 2017

Revision Date: Aug 15, 2017

1.Identification

1.1 GHS Product identifier

Product name 5-methyl-5-(2-methylpropyl)-2(5H)-furanone

1.2 Other means of identification

Product number -
Other names -

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:110296-01-0 SDS

110296-01-0Downstream Products

110296-01-0Relevant academic research and scientific papers

Palladium(II) Chloride Catalyzed Carbonylation of Organic Tellurides with Carbon Monoxide

Ohe, Kouichi,Takahashi, Hidetaka,Uemura, Sakae,Sugita, Nobuyuki

, p. 4859 - 4863 (2007/10/02)

Various organic tellurides react with carbon monoxide (1 atm) at room temperature in methanol in the presence of PdCl2 and Et3N to afford the corresponding methyl carboxylates in good to excellent yields.The reaction is catalytic in PdCl2 when a suitable reoxidant such as CuCl2, CuCl/O2, FeCl3 or Ce(NH4)2(NO3)6 is present.The combination of this carbonylation with phenyltellurenylation of arylacetylenes and propargylic alcohols makes it possible to prepare ring-substituted cis-methyl cinnamates and Δα,β-butenolides, respectively.Both monomeric and dimeric palladium complexes, (Ph2Te)2PdCl2 and 2, react readily with CO to give a high yield of methyl benzoate.The key step of the present carbonylation is proposed to be the migration of an organic moiety from Te to Pd (transmetalation) in organic telluride-PdCl2 complexes, presumably formed in situ, to afford organopalladium compounds.

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