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1,4-Benzodioxin-2(3H)-one, 3-(phenylmethylene)- is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

109028-91-3

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109028-91-3 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 109028-91-3 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,0,9,0,2 and 8 respectively; the second part has 2 digits, 9 and 1 respectively.
Calculate Digit Verification of CAS Registry Number 109028-91:
(8*1)+(7*0)+(6*9)+(5*0)+(4*2)+(3*8)+(2*9)+(1*1)=113
113 % 10 = 3
So 109028-91-3 is a valid CAS Registry Number.

109028-91-3Downstream Products

109028-91-3Relevant academic research and scientific papers

Vinylphosphonium salt mediated reaction between alkyl propiolates and aminophenols or hydroxyphenols

Yavari, Issa,Souri, Sanaz,Sirouspour, Mehdi,Djahaniani, Hoorieh

, p. 3243 - 3249 (2008/09/17)

Addition of catechol to methyl propiolate or ethyl phenylpropiolate in the presence of Ph3P leads to methyl 2-(1,3-benzodioxol-2-yl)acetate or 3-(1-phenylmethylidene)-1,4-benzodioxin-2-one. 2-Aminophenols react with alkyl propiolates in the pre

Rhodium Carbenoid O-H Insertion Reactions With Phenols; A Facile Method for the Synthesis of Trialkyl 2-Aryloxyphosphonoacetates and Their Use in the Preparation of 2-Aryloxy-3-phenylpropanoates.

Haigh, David

, p. 3177 - 3194 (2007/10/02)

A variety of substituted phenols undergo a facile and hitherto unreported rhodium carbenoid mediated O-H insertion reaction with trialkyl 2-diazophosphonoacetates 7 to afford the corresponding trialkyl 2-aryloxyphosphonoacetates 5 in generally good to exc

RING OPENING AND RING-CHAIN TAUTERISM IN 2-CARBALKOXY- AND 2-ACYL-2,3-DIHYDRO-1,4-BENZODIOXINS.

Rosnati, Vittorio,Salimbeni, Aldo

, p. 4541 - 4548 (2007/10/02)

The behaviour of benzodioxin esters 1a-c and ketones 2a-c under the action of K2CO3 in acetone and of NaH in DMSO has been studied; the experiments were also carried out in the presence of scavengers of phenolic intermediates or products.Under the action

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