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N-(1,3-dihydroxy-2-(hydroxymethyl)propan-2-yl)benzamide is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

99430-47-4

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99430-47-4 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 99430-47-4 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 9,9,4,3 and 0 respectively; the second part has 2 digits, 4 and 7 respectively.
Calculate Digit Verification of CAS Registry Number 99430-47:
(7*9)+(6*9)+(5*4)+(4*3)+(3*0)+(2*4)+(1*7)=164
164 % 10 = 4
So 99430-47-4 is a valid CAS Registry Number.

99430-47-4Relevant academic research and scientific papers

The Synthesis and Characterization of Aromatic Hybrid Anderson-Evans POMs and their Serum Albumin Interactions: The Shift from Polar to Hydrophobic Interactions

Al-Sayed, Emir,Blazevic, Amir,Roller, Alexander,Rompel, Annette

, p. 17800 - 17807 (2015)

Four aromatic hybrid Anderson polyoxomolybdates with Fe3+ or Mn3+ as the central heteroatom have been synthesized by using a pre-functionalization protocol and characterized by using single-crystal X-ray diffraction, FTIR, ESI-MS, s

Copper-Catalyzed Enantioselective Synthesis of Oxazolines from Aminotriols via Asymmetric Desymmetrization

Yamamoto, Kosuke,Tsuda, Yutaro,Kuriyama, Masami,Demizu, Yosuke,Onomura, Osamu

supporting information, p. 840 - 844 (2020/02/28)

A copper-catalyzed enantioselective transformation of tris(hydroxymethyl)aminomethane-derived aminotriols was developed to provide multisubstituted oxazolines with a tetrasubstituted carbon center. The present transformation consisted of sequential reacti

Enantioselective formation of tert-alkylamines by desymmetrization of 2-substituted serinols

Hong, Mi Sook,Kim, Tae Woo,Jung, Byunghyuck,Kang, Sung Ho

supporting information; experimental part, p. 3290 - 3296 (2009/04/10)

Novel enantioselective desymmetrization of 2-substituted 2-amino-1,3-propanediols has been established to generate asymmetric quaternary carbon centers comprising an amino group. Enantioselective as well as chemical conversion proved to be greatly dependent on the protecting group of the amino group in the substrate, desymmetrizing reagent, base, solvent, and naturally, catalyst. The highly effective desymmetrization has been implemented by using N-benzoylated substrates with benzoyl Chloride and triethylamine in the presence of tetraphenylbisoxazoline (24)-CuCl2 complex in THF at ambient temperature. An extensive survey of catalysts revealed that dimethylmalonate- bridged bisoxazoline-CuCl2 complexes were superior. Among them, the tetraphenylbisoxazoline (24)-CuCl2 complex turned out to work most efficiently with a wide array of the substrates. All the examined substrates, with the exception of 2-phenylserinol 36, were desymmetrized in the presence of 24-CuCl2 complex to give high enantioselectivities ranging from 85 to 95% ee. Complementary use of the diisopropylbisoxazoline (22)-CuCl2 complex has remedied the mediocre desymmetrization of 36 to give a significantly improved enantioselectivity from 63 to 83% ee.

CONFORMATION OF 5,5-DISUBSTITUTED 2,2-DIMETHYL-1,3-DIOXANES

Kraiz, B. O.

, p. 387 - 392 (2007/10/02)

It was established by PMR spectral data that in solutions of derivatives of 5-acetoxymethyl-, 5-methyl-, and 5-hydroxymethyl-2,2-dimethyl-1,3-dioxanes with nitrogen-containing substituents (2,4-disubstituted 1,3,5-triazin-6-ylamino, benzamido, and nitro g

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