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Benzoic acid, 2-hydroxy-5-(2-hydroxyethoxy)-, methyl ester is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

137819-31-9

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137819-31-9 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 137819-31-9 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,3,7,8,1 and 9 respectively; the second part has 2 digits, 3 and 1 respectively.
Calculate Digit Verification of CAS Registry Number 137819-31:
(8*1)+(7*3)+(6*7)+(5*8)+(4*1)+(3*9)+(2*3)+(1*1)=149
149 % 10 = 9
So 137819-31-9 is a valid CAS Registry Number.

137819-31-9Downstream Products

137819-31-9Relevant academic research and scientific papers

Mechanistic Studies of the Deslongchamps Annulation

Kreibich, Michael,Petrovi?, Denis,Brückner, Reinhard

supporting information, p. 1116 - 1133 (2018/02/14)

The Cs2CO3-mediated annulations ("Deslongchamps annulations") of three spirocyclic benzoquinone monoketals 5b-d with an ester or acyl substituent at C-2 to two tert-butyl esters of λδ-unsaturated β-ketocarboxyl acids ("Nazarov reagents" 2a,b) were monitored 1H NMR spectroscopically. This revealed that a primary product, by all likelihood the Michael adduct, forms fast and prior to the appearance of the Deslongchamps adduct. These primary products form reversibly. This was proved by two crossover and four scavenging experiments. Therein, components already incorporat.

Deslongchamps annulations with benzoquinone monoketals

Petrovic, Denis,Brueckner, Reinhard

supporting information; experimental part, p. 6524 - 6527 (2012/02/01)

The so-called Deslongchamps annulation of deprotonated γ, δ-unsaturated β-ketoesters 15 to 2-(alkoxycarbonyl)cyclohex-2-en-1- ones or similarly activated cyclohex-2-en-1-ones offers a versatile access to various kinds of decalindiones. The scope of Deslon

A route for the enantioselective total synthesis of antheridic acid, the antheridium-inducing factor from anemia phyllitidis

Corey,Kigoshi, Hideo

, p. 5025 - 5028 (2007/10/02)

An effective route for the total synthesis of antheridic acid (1) has been devised in which the initial chiral intermediate 7 is generated by enantioselective catalytic reduction and transformed in a stereocontrolled fashion into key intermediates 9, 10, 13, and 2.

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