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2H-Pyran-5-carboxylic acid, 2,2-dimethyl-6-(4-methyl-1,3-pentadienyl)-, ethyl ester, (E)- is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

114114-79-3

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114114-79-3 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 114114-79-3 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,1,4,1,1 and 4 respectively; the second part has 2 digits, 7 and 9 respectively.
Calculate Digit Verification of CAS Registry Number 114114-79:
(8*1)+(7*1)+(6*4)+(5*1)+(4*1)+(3*4)+(2*7)+(1*9)=83
83 % 10 = 3
So 114114-79-3 is a valid CAS Registry Number.

114114-79-3SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 16, 2017

Revision Date: Aug 16, 2017

1.Identification

1.1 GHS Product identifier

Product name 1E ethyl 2,2-dimethyl-6-(4-methylpenta-1,3-dienyl)-2H-pyran-5-carboxylate

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:114114-79-3 SDS

114114-79-3Relevant academic research and scientific papers

New Insights on the Reaction of Alkyl 3-Oxo-4-(triphenylphosphoranylidene)butanoate and Aldehydes under Concentrated Condensation Conditions. One-Pot Synthesis of Highly functionalised 6-Oxocyclohex-4-ene-1,3-dicarboxylates

Moorhoff, Cornelis M.,Schneider, David F.,Winkler, Dave

, p. 3461 - 3483 (2007/10/03)

New annulation methodologies for the construction of substituted cyclohex-2-enones are important in organic synthesis. In this paper wee describe a new one-pot synthesis of substituted cyclohexenonedicarboxylates in maximum yield of 52 percent from the condensation of alkyl 3-oxo-4-(triphenylphosphoranylidene)-butanoate 1 and aldehydes.

CONDENSATION OF ETHYL AND METHYL 4-(TRIPHENYLPHOSPHORANYLIDENE)-3-OXOBUTANOATE WITH ENALS

Moorhoff, Cornelis M.,Schneider, David F.

, p. 4721 - 4724 (2007/10/02)

The manipulation of the mode of reaction of 4-(phosphoranylidene)-3-oxobutanoates with enals and a resulting new synthesis of ethyl β-safranate have been explored.

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