100858-32-0

  • Product Name:(S)-1-CBZ-3-PYRROLIDINOL
  • Molecular Formula:C12H15NO3
  • Purity:99%
  • Molecular Weight:221.256
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Product Details

pd_meltingpoint:71-77 °C

Factory Sells Best Quality (S)-1-CBZ-3-PYRROLIDINOL 100858-32-0 with USP

  • Molecular Formula:C12H15NO3
  • Molecular Weight:221.256
  • Vapor Pressure:3.75E-06mmHg at 25°C 
  • Melting Point:71-77 °C 
  • Refractive Index:1.589 
  • Boiling Point:370.7 °C at 760 mmHg 
  • PKA:14.72±0.20(Predicted) 
  • Flash Point:178 °C 
  • PSA:49.77000 
  • Density:1.263 g/cm3 
  • LogP:1.32770 

(S)-1-CBZ-3-PYRROLIDINOL 95(Cas 100858-32-0) Usage

InChI:InChI=1/C12H15NO3/c14-11-6-7-13(8-11)12(15)16-9-10-4-2-1-3-5-10/h1-5,11,14H,6-9H2/t11-/m0/s1

100858-32-0 Relevant articles

Chiral Synthesis via Organoboranes. 6. Hydroboration. 74. Asymmetric Hydroboration of Representative Heterocyclic Olefins with Diisopinocamphenylborane. Synthesis of Heterocyclic Boronates and Heterocyclic Alcohols of Very High Enantiomeric Purity

Brown, Herbert C.,Prasad, J. V. N. Vara

, p. 2049 - 2054 (1986)

The hydroboration of representative hete...

Stereo-complementary bioreduction of saturated N-heterocyclic ketones

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Regio- and stereoselective biohydroxylations with a recombinant escherichia coli expressing P450pyr monooxygenase of sphingomonas Sp. HXN-200

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A recombinant Escherichia coli expressin...

Ultrafast chiral separations for high throughput enantiopurity analysis

Barhate, Chandan L.,Joyce, Leo A.,Makarov, Alexey A.,Zawatzky, Kerstin,Bernardoni, Frank,Schafer, Wes A.,Armstrong, Daniel W.,Welch, Christopher J.,Regalado, Erik L.

supporting information, p. 509 - 512 (2017/01/13)

Recent developments in fast chromatograp...

BRUTON'S TYROSINE KINASE INHIBITORS

-

Page/Page column 81; 82, (2014/05/24)

Disclosed herein are compounds that form...

100858-32-0 Process route

benzyl 3-oxopyrrolidine-1-carboxylate
130312-02-6

benzyl 3-oxopyrrolidine-1-carboxylate

(S)-3-hydroxy-1-pyrrolidinecarboxylic acid phenylmethyl ester
100858-32-0

(S)-3-hydroxy-1-pyrrolidinecarboxylic acid phenylmethyl ester

Conditions
Conditions Yield
With recombinant Rhodococcus erythropolis DSM 43297 ketoredutase; nicotinamide adenine dinucleotide; In aq. phosphate buffer; isopropyl alcohol; at 50 ℃; for 21h; pH=7.0; stereoselective reaction; Enzymatic reaction;
86%
With water; at 20 ℃; for 72h; enantioselective reaction;
41%
benzyl chloroformate
501-53-1,94274-21-2

benzyl chloroformate

3-hydroxypyrrolidine
100243-39-8

3-hydroxypyrrolidine

(S)-3-hydroxy-1-pyrrolidinecarboxylic acid phenylmethyl ester
100858-32-0

(S)-3-hydroxy-1-pyrrolidinecarboxylic acid phenylmethyl ester

Conditions
Conditions Yield
With triethylamine; In dichloromethane; at 5 - 20 ℃; for 48h;
92%
With triethylamine; In dichloromethane; at 0 ℃; for 2h;

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