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1,2-Propanediol, 3-(4-chlorophenoxy)-, 1-nitrate is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

217322-53-7

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217322-53-7 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 217322-53-7 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 2,1,7,3,2 and 2 respectively; the second part has 2 digits, 5 and 3 respectively.
Calculate Digit Verification of CAS Registry Number 217322-53:
(8*2)+(7*1)+(6*7)+(5*3)+(4*2)+(3*2)+(2*5)+(1*3)=107
107 % 10 = 7
So 217322-53-7 is a valid CAS Registry Number.

217322-53-7Downstream Products

217322-53-7Relevant academic research and scientific papers

Lipase-catalyzed kinetic resolution of the racemic mixtures of 1- aryloxy-3-nitrato-and-1-aryloxy-3-azido-2-propanols

Pchelka, Beata,Radomska, Justyna,Plenkiewicz, Jan

, p. 4355 - 4364 (1998)

The racemic mixtures of 1-aryloxy-3-nitrato-2-propanols and 1-aryloxy- 3-azido-2-propanols were resolved with moderate selectivity by the lipase- mediated acylation with vinyl acetate. The effects of the nature, position, and spatial requirements of the p

Efficient regio- and stereoselective conversions of oxiranes and aziridines into β-(nitrooxy)-substituted alcohols and amines by using bismuth nitrate

Das, Biswanath,Krishnaiah, Maddeboina,Venkateswarlu, Katta,Reddy, Vtukuri Saidi

, p. 110 - 113 (2007/10/03)

Oxiranes and aziridines efficiently undergo ring opening with bismuth nitrate at room temperature to furnish the corresponding β-(nitrooxy)- substituted alcohols and amines respectively. The conversions are highly regio- and stereoselective and afford the

Zirconyl nitrate mediated regioselective ring opening of epoxides and aziridines: an easy synthesis of β-nitrato-alcohols and -sulfonamides

Das, Biswanath,Krishnaiah, Maddeboina,Venkateswarlu, Katta

, p. 6027 - 6029 (2007/10/03)

Epoxides and aziridines are cleaved efficiently and regioselectively in the presence of zirconyl nitrate at room temperature to afford the corresponding β-nitrato-alcohols and -sulfonamides, respectively, in high yields.

Resolution of racemic 3-aryloxy-1-nitrooxypropan-2-ols by lipase-catalyzed enantioselective acetylation

Pchelka, Beata Krystyna,Loupy, Andre,Plenkiewicz, Jan,Petit, Alain,Blanco, Luis

, p. 2109 - 2119 (2007/10/03)

Both (R)- and (S)-enantiomers of 3-aryloxy-1-nitrooxypropan-2-ols (R)-(-)-1, (S)-(+)-2 were prepared in high enantiomeric excess by lipase from Pseudomonas cepacia (Amano PS) or Pseudomonas fluorescens (Amano AK)-catalyzed acetylation of racemic alcohols 1a-g with vinyl acetate in n-hexane at 4 or 22°C. The enantioselectivity of this transformation was dependent on the substitution pattern of the aryl ring with E-values ranging from 31 to 111.

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