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2,2-dimethyl-4-(2,2-dimethoxy-1-(4-methoxyphenylamino)ethyl)-1,3-dioxan-5-one is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

863971-72-6

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863971-72-6 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 863971-72-6 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 8,6,3,9,7 and 1 respectively; the second part has 2 digits, 7 and 2 respectively.
Calculate Digit Verification of CAS Registry Number 863971-72:
(8*8)+(7*6)+(6*3)+(5*9)+(4*7)+(3*1)+(2*7)+(1*2)=216
216 % 10 = 6
So 863971-72-6 is a valid CAS Registry Number.

863971-72-6Downstream Products

863971-72-6Relevant academic research and scientific papers

Organic solvent-free, enantio- and diastereoselective, direct Mannich reaction in the presence of water

Hayashi, Yujiro,Urushima, Tatsuya,Aratake, Seiji,Okano, Tsubasa,Obi, Kazuki

, p. 21 - 24 (2008/09/17)

An organocatalyst-mediated, asymmetric Mannich reaction in the presence of water without using organic solvents has been developed. A highly reactive siloxytetrazole hybrid catalyst has been developed for the reaction of dimethoxyacetaldehyde, while the s

Efficient entry to amino sugars and derivatives via asymmetric organocatalytic Mannich reactions

Enders, Dieter,Grondal, Christoph,Vrettou, Marianna

, p. 3597 - 3604 (2008/03/14)

An efficient biomimetic C3+Cn entry to amino sugars and derivatives via a direct asymmetric organocatalytic Mannich methodology employing 2,2-dimethyl-1,3-dioxan-5-one as a dihydroxyacetone phosphate equivalent and N-PMP or N-Boc pro

Asymmetric synthesis of selectively protected amino sugars and derivatives by a direct organocatalytic mannich reaction

Enders, Dieter,Grondal, Christoph,Vrettou, Marianna,Raabe, Gerhard

, p. 4079 - 4083 (2007/10/03)

(Chemical Equation Presented) Short and sweet: Starting from the commercially available precursors 1-3, selectively protected amino sugars and derivatives are obtained in one step and with high diastereo- and enantiomeric purity by means of a proline-cata

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