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107474-79-3

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107474-79-3 Usage

Chemical Properties

clear colourless liquid

Uses

(+)-1-(9-Fluorenyl)ethyl Chloroformate is an analytical reagent for direct and indirect chiral separation of amino acids by capillary electrophoresis.

General Description

(+)-1-(9-Fluorenyl)ethyl chloroformate is a highly fluorescent compound1 commonly used as a chiral derivatizing agent for the separation of racemates prior to reversed-phase HPLC analysis.

Check Digit Verification of cas no

The CAS Registry Mumber 107474-79-3 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,0,7,4,7 and 4 respectively; the second part has 2 digits, 7 and 9 respectively.
Calculate Digit Verification of CAS Registry Number 107474-79:
(8*1)+(7*0)+(6*7)+(5*4)+(4*7)+(3*4)+(2*7)+(1*9)=133
133 % 10 = 3
So 107474-79-3 is a valid CAS Registry Number.
InChI:InChI=1/C16H13ClO2/c1-10(19-16(17)18)15-13-8-4-2-6-11(13)12-7-3-5-9-14(12)15/h2-10,15H,1H3/t10-/m1/s1

107474-79-3 Well-known Company Product Price

  • Brand
  • (Code)Product description
  • CAS number
  • Packaging
  • Price
  • Detail
  • Aldrich

  • (335975)    18 mM in acetone, for chiral derivatization

  • 107474-79-3

  • 335975-1ML

  • 2,819.70CNY

  • Detail
  • Aldrich

  • (335975)    18 mM in acetone, for chiral derivatization

  • 107474-79-3

  • 335975-10ML

  • 14,157.00CNY

  • Detail
  • Sigma-Aldrich

  • (23182)  (+)-1-(9-Fluorenyl)ethylchloroformatesolution  for chiral derivatization, ≥18 mM in acetone

  • 107474-79-3

  • 23182-10ML-F

  • 7,792.20CNY

  • Detail
  • Sigma-Aldrich

  • (23182)  (+)-1-(9-Fluorenyl)ethylchloroformatesolution  for chiral derivatization, ≥18 mM in acetone

  • 107474-79-3

  • 23182-10X1ML-F

  • 8,570.25CNY

  • Detail

107474-79-3SDS

SAFETY DATA SHEETS

According to Globally Harmonized System of Classification and Labelling of Chemicals (GHS) - Sixth revised edition

Version: 1.0

Creation Date: Aug 18, 2017

Revision Date: Aug 18, 2017

1.Identification

1.1 GHS Product identifier

Product name (+)-1-(9-FLUORENYL)ETHYL CHLOROFORMATE

1.2 Other means of identification

Product number -
Other names -

1.3 Recommended use of the chemical and restrictions on use

Identified uses For industry use only.
Uses advised against no data available

1.4 Supplier's details

1.5 Emergency phone number

Emergency phone number -
Service hours Monday to Friday, 9am-5pm (Standard time zone: UTC/GMT +8 hours).

More Details:107474-79-3 SDS

107474-79-3Relevant articles and documents

(S)-(?)-Fluorenylethylchloroformate (FLEC); preparation using asymmetric transfer hydrogenation and application to the analysis and resolution of amines

Amin, Mohammad A.,Camerino, Michelle A.,Mountford, Simon J.,Ma, Xiao,Manallack, David T.,Chalmers, David K.,Wills, Martin,Thompson, Philip E.

, (2019/09/19)

Fluorenylethylchoroformate (FLEC) is a valuable chiral derivatisation reagent that is used for the resolution of a wide variety of chiral amines. Herein, we describe an improved preparation of (S)-(?)-FLEC using an efficient asymmetric catalytic transfer hydrogenation as the key step. We also demonstrate the application of FLEC as a chiral Fmoc equivalent for chiral resolution, with facile deprotection, of tetrahydroquinaldines, and its capacity for inducing regioselective outcomes in nitration reactions.

(+)-Fluorenylethylchloroformate (FLEC)-improved synthesis for application in chiral analysis and peptidomimetic synthesis

Camerino, Michelle A.,Chalmers, David K.,Thompson, Philip E.

, p. 2571 - 2573 (2013/06/05)

An efficient synthesis of the enantiomers of fluorenylethylchloroformate (FLEC) has been achieved that allows the routine application of the reagent for the resolution of chiral amines including unusual amino acids. The utility of the fluorenylethoxycarbonyl (Feoc) group as a chiral Fmoc equivalent, for combined resolution and protection of amino acids, in solid phase peptide synthesis is also shown.

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