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184714-56-5

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184714-56-5 Usage

General Description

"(R)-4-Benzyl-3-chloroacetyl-2-" is a chemical compound with the molecular formula C11H11ClO2. It is a derivative of 2-butyllactone and is classified as a chiral compound. This chemical has potential applications in the field of organic chemistry, particularly in the synthesis of complex molecules and pharmaceutical research. Its structure contains a benzyl group, a chlorine atom, and an acetyl group, all of which contribute to its distinct properties and potential reactivity in chemical reactions. Further study and research are needed to fully understand the specific uses and implications of this chemical compound.

Check Digit Verification of cas no

The CAS Registry Mumber 184714-56-5 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,8,4,7,1 and 4 respectively; the second part has 2 digits, 5 and 6 respectively.
Calculate Digit Verification of CAS Registry Number 184714-56:
(8*1)+(7*8)+(6*4)+(5*7)+(4*1)+(3*4)+(2*5)+(1*6)=155
155 % 10 = 5
So 184714-56-5 is a valid CAS Registry Number.
InChI:InChI=1/C12H12ClNO3/c13-7-11(15)14-10(8-17-12(14)16)6-9-4-2-1-3-5-9/h1-5,10H,6-8H2/t10-/m1/s1

184714-56-5 Well-known Company Product Price

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  • Aldrich

  • (534951)  (R)-4-Benzyl-3-chloroacetyl-2-oxazolidinone  97%

  • 184714-56-5

  • 534951-500MG

  • 857.61CNY

  • Detail

184714-56-5SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 15, 2017

Revision Date: Aug 15, 2017

1.Identification

1.1 GHS Product identifier

Product name (4R)-4-benzyl-3-(2-chloroacetyl)-1,3-oxazolidin-2-one

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:184714-56-5 SDS

184714-56-5Relevant articles and documents

Synthesis and application of N-3,5-dinitrobenzoyl and C3 symmetric diastereomeric chiral stationary phases

Ryoo, Jae Jeong,Yu, Jeong Jae

, (2022/01/20)

Three diastereomeric chiral compounds, namely, (R,R)-(+)-2-amino-1,2-diphenylethanol, (1S,2R)-(+)-2-amino-1,2-diphenylethanol, and (1R,2R)-(+)-1,2-diphenylethylenediamine were used as starting materials for preparing three N-3,5-dinitrobenzoyl derivative

Synthesis of new C3 symmetric amino acid- and aminoalcohol-containing chiral stationary phases and application to HPLC enantioseparations

Yu, Jeongjae,Armstrong, Daniel W.,Ryoo, Jae Jeong

, p. 74 - 84 (2017/12/26)

We recently reported a new C3-symmetric (R)-phenylglycinol N-1,3,5-benzenetricarboxylic acid-derived chiral high-performance liquid chromatography (HPLC) stationary phase (CSP 1) that demonstrated better results as compared to a previously described N-3,5-dintrobenzoyl (DNB) (R)-phenylglycinol-derived CSP. Over a decade ago, (S)-leucinol, (R)-phenylglycine, and (S)-leucine derivatives were used as the starting materials of 3,5-DNB-based Pirkle-type CSPs for chiral separation. In this study, three new C3-symmetric CSPs (CSP 2, 3, and 4) were prepared by combining the ideas and results mentioned above. Here we describe the synthetic procedures and applications of the new C3-symmetric CSPs (CSP 2–CSP 4).

Liquid Chromatographic Resolution of Racemic 2-Oxazolidinones and their Analogs on Seven Pirkle-Type Chiral Stationary Phases

Yu, Jeong Jae,Hyun, Myung Ho,Armstrong, Daniel W.,Breitbach, Zachary S.,Ryoo, Jae Jeong

, p. 723 - 726 (2015/07/20)

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