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(4S,5S)-5-(hydroxymethyl)-4-(phenylthio)dihydrofuran-2(3H)-one is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

1403352-71-5

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1403352-71-5 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 1403352-71-5 includes 10 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 7 digits, 1,4,0,3,3,5 and 2 respectively; the second part has 2 digits, 7 and 1 respectively.
Calculate Digit Verification of CAS Registry Number 1403352-71:
(9*1)+(8*4)+(7*0)+(6*3)+(5*3)+(4*5)+(3*2)+(2*7)+(1*1)=115
115 % 10 = 5
So 1403352-71-5 is a valid CAS Registry Number.

1403352-71-5Downstream Products

1403352-71-5Relevant articles and documents

Regioselective Dehydration of Sugar Thioacetals under Mild Conditions

Szpara, Rachel,Goyder, Alexander,Porter, Michael J.,Hailes, Helen C.,Sheppard, Tom D.

supporting information, p. 2488 - 2492 (2021/04/13)

Sugars are abundant in waste biomass, making them sustainable chiral building blocks for organic synthesis. The demand for chiral saturated heterocyclic rings for pharmaceutical applications is increasing as they provide well-defined three-dimensional frameworks that show increased metabolic resistance. A range of sugar thioacetals can be dehydrated selectively at C-2 under mild basic conditions, and the resulting ketene thioacetals can be applied to the production of useful chiral building blocks via further selective dehydration reactions.

Total synthesis of branimycin: An evolutionary approach

Enev, Valentin S.,Felzmann, Wolfgang,Gromov, Alexey,Marchart, Stefan,Mulzer, Johann

, p. 9651 - 9668 (2012/09/21)

The first total synthesis of the macrolactone antibiotic branimycin (4) has been described. The key disconnection leads to a cis-dehydrodecalone core and a polyketide side chain which are connected via organometallic addition. The dehydrodecalone core was targeted via altogether five different approaches featuring various kinds of chiral elements and ring-closing methodology. In the end the most successful method starting from diepoxynaphthalene 109 was chosen to carry on with the synthesis. Thus the oxygen functions and carbon appendages were introduced via organometallic desymmetrization reactions to generate epoxy ketone 107, to which vinyl iodide 11 was added after conversion into the organolithium species. The synthesis was completed by introducing the ester side chain via Michael addition and subsequent macrolactonization. Competitive approach: The first total synthesis of the macrolactone antibiotic branimycin is described (see figure). The dehydrodecalin core was targeted via five competing approaches featuring various kinds of chiral elements and ring-closing methodology. In this "Darwinian" struggle the most successful route emerged and led to the completion of the synthesis. Copyright

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