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2272-55-1

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2272-55-1 Usage

Description

Oxiranecarboxylic acid, 3-phenyl-, ethyl ester, transis a stable, colorless liquid with a sweet, floral odor. It is a chemical compound derived from trans-phenylglycidic acid and is commonly used in the manufacturing of various products such as pharmaceuticals, pesticides, and perfumes. This versatile and valuable component is also known for its potential use as an intermediate in organic synthesis. However, it is important to handle with care due to its potential to cause irritation to the eyes, skin, and respiratory system, and it should be stored in a cool, dry place away from direct sunlight and heat sources.

Uses

Used in Pharmaceutical Industry:
Oxiranecarboxylic acid, 3-phenyl-, ethyl ester, transis used as an intermediate in the synthesis of various pharmaceutical compounds. Its unique chemical structure allows for the development of new drugs with potential therapeutic applications.
Used in Pesticide Industry:
This chemical compound is used as a key ingredient in the formulation of certain pesticides. Its ability to effectively control pests and protect crops makes it a valuable component in the agricultural sector.
Used in Perfume Industry:
Oxiranecarboxylic acid, 3-phenyl-, ethyl ester, transis used as a fragrance ingredient in the perfume industry. Its sweet, floral odor contributes to the creation of various scent profiles in perfumes and other fragranced products.
Used in Organic Synthesis:
As an intermediate in organic synthesis, Oxiranecarboxylic acid, 3-phenyl-, ethyl ester, transplays a crucial role in the development of new chemical compounds and materials. Its versatility in chemical reactions allows for the synthesis of a wide range of products across various industries.

Check Digit Verification of cas no

The CAS Registry Mumber 2272-55-1 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 2,2,7 and 2 respectively; the second part has 2 digits, 5 and 5 respectively.
Calculate Digit Verification of CAS Registry Number 2272-55:
(6*2)+(5*2)+(4*7)+(3*2)+(2*5)+(1*5)=71
71 % 10 = 1
So 2272-55-1 is a valid CAS Registry Number.

2272-55-1SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 17, 2017

Revision Date: Aug 17, 2017

1.Identification

1.1 GHS Product identifier

Product name ethyl (2R,3S)-3-phenyloxirane-2-carboxylate

1.2 Other means of identification

Product number -
Other names ethyl trans-3-phenyloxiranecarboxylate

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:2272-55-1 SDS

2272-55-1Relevant articles and documents

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Seyden-Penne et al.

, p. 2649,2655 (1970)

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Towards a General Understanding of Carbonyl-Stabilised Ammonium Ylide-Mediated Epoxidation Reactions

Novacek, Johanna,Roiser, Lukas,Zielke, Katharina,Robiette, Rapha?l,Waser, Mario

supporting information, p. 11422 - 11428 (2016/08/03)

The key factors for carbonyl-stabilised ammonium ylide-mediated epoxidation reactions were systematically investigated by experimental and computational means and the hereby obtained energy profiles provide explanations for the observed experimental results. In addition, we were able to identify the first tertiary amine-based chiral auxiliary that allows for high enantioselectivities and high yields for such epoxidation reactions.

Method for Preparing Optically Pure (-)-Clausenamide Compound

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Paragraph 0042; 0043; 0044; 0045, (2014/07/23)

Disclosed in the present invention is a method for preparing a (?)-clausenamide compound of formula (I), comprising: firstly, catalyzing the asymmetrical epoxidation of trans-cinnamate using a chiral ketone derived from fructose or a hydrate thereof as a catalyst, and then subjecting the product to transesterification, oxidation, cyclization and reduction successively to finally obtain the optically pure (?)-clausenamide compound of formula (I).

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