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(R)-3-benzyl-1H-furo[3,4-c]isochromene-1,5(3H)-dione is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

1611478-85-3

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1611478-85-3 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 1611478-85-3 includes 10 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 7 digits, 1,6,1,1,4,7 and 8 respectively; the second part has 2 digits, 8 and 5 respectively.
Calculate Digit Verification of CAS Registry Number 1611478-85:
(9*1)+(8*6)+(7*1)+(6*1)+(5*4)+(4*7)+(3*8)+(2*8)+(1*5)=163
163 % 10 = 3
So 1611478-85-3 is a valid CAS Registry Number.

1611478-85-3Downstream Products

1611478-85-3Relevant academic research and scientific papers

Chiral Pool-Based Synthesis of Naphtho-Fused Isocoumarins

Raza, Abdul Rauf,Saddiqa, Aisha,?akmak, Osman

, p. 951 - 957 (2015/11/16)

A variety of chiral derivatives of benzo[d]naphtho[1,2-b]pyran-6-one were prepared in a single step by Et3N-mediated condensation of homophthalic anhydride with different derivatives of (S)-amino acid chlorides at -5 °C by employing a chiral pool methodology. Chirality 27:951-957, 2015.

Chiron based synthesis of isocoumarins: Reactivity of α-substituted carboxylic acids

Saddiqa, Aisha,Raza, Abdul R.,Black, David Stc.,Kumar, Naresh

, p. 736 - 743 (2014/06/09)

The asymmetric synthesis of a novel (S)-isocoumarin has been attempted in a single step by the coupling of homophthalic acid with (S)-N-protected amino acids and α-chloroacids at high temperature by exploiting a chiral pool methodology. The coupling of homophthalic acid with N-protected (S)-amino acids gave exclusion of the carboxyl/alkyl group. However, coupling of homophthalic acid with α-chloroacids afforded asymmetric isocoumarins in high yield.

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