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54882-04-1

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54882-04-1 Usage

General Description

Phenylsulfinylacetic acid ethyl ester is a chemical compound with the molecular formula C10H12O3S. It is an ethyl ester of phenylsulfinylacetic acid, and it is commonly used as a reagent in organic synthesis. PHENYLSULFINYLACETIC ACID ETHYL ESTER is a colorless, aromatic liquid that is soluble in organic solvents. It is known for its role in the synthesis of various pharmaceuticals and other organic compounds due to its ability to undergo a variety of chemical reactions. Phenylsulfinylacetic acid ethyl ester is also used as a building block in the synthesis of complex molecules, making it an important compound in the field of organic chemistry.

Check Digit Verification of cas no

The CAS Registry Mumber 54882-04-1 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 5,4,8,8 and 2 respectively; the second part has 2 digits, 0 and 4 respectively.
Calculate Digit Verification of CAS Registry Number 54882-04:
(7*5)+(6*4)+(5*8)+(4*8)+(3*2)+(2*0)+(1*4)=141
141 % 10 = 1
So 54882-04-1 is a valid CAS Registry Number.
InChI:InChI=1/C10H12O3S/c1-2-13-10(11)8-14(12)9-6-4-3-5-7-9/h3-7H,2,8H2,1H3

54882-04-1 Well-known Company Product Price

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  • TCI America

  • (P1135)  Ethyl Phenylsulfinylacetate  >85.0%(GC)

  • 54882-04-1

  • 5g

  • 1,830.00CNY

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54882-04-1SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 12, 2017

Revision Date: Aug 12, 2017

1.Identification

1.1 GHS Product identifier

Product name Ethyl Phenylsulfinylacetate

1.2 Other means of identification

Product number -
Other names ethyl 2-(benzenesulfinyl)acetate

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:54882-04-1 SDS

54882-04-1Relevant articles and documents

Byproduct formation during the biosynthesis of spinosyn A and evidence for an enzymatic interplay to prevent its formation

Choi, Sei-hyun,Franklin, Joseph Livy,Huang, Teng-Yi,Hung, Shang-Cheng,Jeon, Byung-sun,Kim, Namho,Liu, Hung-wen,Ruszczycky, Mark W.

supporting information, (2021/11/30)

Biosynthesis of spinosyn A in Saccharopolyspora spinosa involves a 1,4-dehydration followed by an intramolecular [4 + 2]-cycloaddition catalyzed by SpnM and SpnF, respectively. The cycloaddition also takes place in the absence of SpnF leading to questions

Synthesis of: N -alkylated 2-pyridones through Pummerer type reactions of activated sulfoxides and 2-fluoropyridine derivatives

Hu, Gang,Xu, Jiaxi,Li, Pingfan

, p. 4151 - 4158 (2018/06/12)

N-Alkylated 2-pyridone products were obtained in good to excellent yields through a one-pot procedure involving either normal or interrupted Pummerer reactions between triflic anhydride activated sulfoxides and 2-fluoropyridine derivatives, followed by hydrolysis. This is a rare case that uses 2-fluoropyridine as a nucleophile in Pummerer type reactions.

Ammonium salt catalyzed oxidation of organosulfides to organosulfoxydes

Secci, Francesco,Frongia, Angelo,Piras, Pier Paolo

, p. 603 - 605 (2014/01/23)

The selective oxidation of aromatic and aliphatic organosulfides with H2O2/H2O catalyzed by metal free ammonium salts has been explored. Reactions were performed using 2.5-5 mol % of catalyst loadings, isolating the corres

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