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Ethyl O-mesitylsulfonylacetohydroxamate

Product Name
Ethyl O-mesitylsulfonylacetohydroxamate
CAS No.
38202-27-6
Chemical Name
Ethyl O-mesitylsulfonylacetohydroxamate
Synonyms
Ethyl N-(Mesitylsulfonyl)oxyacetiMidate;(E)-ethyl N-(Mesitylsulfonyl)oxyacetiMidate;Ethyl O-mesitylsulfo;ETHYL O-MESITYLSULFONYLACETOHYDROXAMATE;ethyl O-methylsulphonylacetohydroxamate;Ethyl O-methylsulfonylacetohydroxamate.;Ethyl o-(mesitylsulfonyl)acetohydroximate;ethyl O-mesitylenesulfonylacetohydroxamate;Ethyl N-[(mesitylsulfonyl)oxy]ethanimidate;Ethyl O-mesitylsulfonylacetohydroxamate,99%
CBNumber
CB9118081
Molecular Formula
C13H19NO4S
Formula Weight
285.36
MOL File
38202-27-6.mol
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Ethyl O-mesitylsulfonylacetohydroxamate Property

Melting point:
54-56 °C (lit.) 54-58 °C
Boiling point:
381.7±52.0 °C(Predicted)
Density 
1.2483 (rough estimate)
refractive index 
1.6800 (estimate)
storage temp. 
2-8°C
form 
powder to crystal
color 
White to Almost white
Water Solubility 
Insoluble
BRN 
2144156
InChI
InChI=1S/C13H19NO4S/c1-6-17-12(5)14-18-19(15,16)13-10(3)7-9(2)8-11(13)4/h7-8H,6H2,1-5H3
InChIKey
KQCBSWBQAXTILK-UHFFFAOYSA-N
SMILES
C(=NOS(C1=C(C)C=C(C)C=C1C)(=O)=O)(OCC)C
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Safety

Safety Statements 
24/25
WGK Germany 
3
6-9-21
HS Code 
29252900
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Hazard and Precautionary Statements (GHS)

Symbol(GHS)
Signal word
Warning
Hazard statements

H315Causes skin irritation

H319Causes serious eye irritation

Precautionary statements

P264Wash hands thoroughly after handling.

P264Wash skin thouroughly after handling.

P280Wear protective gloves/protective clothing/eye protection/face protection.

P302+P352IF ON SKIN: wash with plenty of soap and water.

P305+P351+P338IF IN EYES: Rinse cautiously with water for several minutes. Remove contact lenses, if present and easy to do. Continuerinsing.

P321Specific treatment (see … on this label).

P332+P313IF SKIN irritation occurs: Get medical advice/attention.

P362Take off contaminated clothing and wash before reuse.

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N-Bromosuccinimide Price

Sigma-Aldrich
Product number
63936
Product name
Ethyl O-(2-mesitylenesulfonyl)acethydroxamate
Purity
purum, ≥97.0% (HPLC)
Packaging
5G
Price
$124
Updated
2025/07/31
Sigma-Aldrich
Product number
63936
Product name
Ethyl O-(2-mesitylenesulfonyl)acethydroxamate
Purity
purum, ≥97.0% (HPLC)
Packaging
25G
Price
$486
Updated
2025/07/31
Sigma-Aldrich
Product number
63936
Product name
Ethyl O-(2-mesitylenesulfonyl)acethydroxamate
Purity
purum, ≥97.0% (HPLC)
Packaging
5g-f
Price
$114
Updated
2021/12/16
TCI Chemical
Product number
M1182
Product name
Ethyl O-Mesitylsulfonylacetohydroxamate [Precursor of the Powerful Aminating Reagent]
Purity
>98.0%(HPLC)(N)
Packaging
1g
Price
$32
Updated
2025/07/31
TCI Chemical
Product number
M1182
Product name
Ethyl O-Mesitylsulfonylacetohydroxamate [Precursor of the Powerful Aminating Reagent]
Purity
>98.0%(HPLC)(N)
Packaging
5g
Price
$93
Updated
2025/07/31
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Ethyl O-mesitylsulfonylacetohydroxamate Chemical Properties,Usage,Production

Chemical Properties

white to light yellow crystalline powder

Synthesis Reference(s)

The Journal of Organic Chemistry, 38, p. 1239, 1973 DOI: 10.1021/jo00946a045

Synthesis

773-64-8

10576-12-2

38202-27-6

Ethyl N-hydroxyacetimidate (2.00 g, 19.4 mmol), N,N-diisopropylethylamine (3.01 g, 23.3 mmol), and 4-dimethylaminopyridine (240 mg, 1.96 mmol) were dissolved in anhydrous dichloromethane (30 mL) and the solution was cooled to 0°C. To the cooled solution was slowly added, with stirring, 2,4,6 -trimethylbenzene-1-sulfonyl chloride (4.66 g, 21.3 mmol) to the cooled solution. The reaction mixture was gradually warmed to room temperature and stirring was continued for 1 hour. Upon completion of the reaction, the reaction was quenched by the addition of water (40 mL) and subsequently extracted with dichloromethane (30 mL, 3 times). The organic layers were combined, dried with anhydrous sodium sulfate and concentrated under reduced pressure to give the crude product. The crude product was purified by silica gel fast column chromatography using a hexane solution of 5% ethyl acetate as eluent to afford ethyl O-(2,4,6-trimethylbenzenesulfonyl)acetohydroxamic acid as a white solid (5.19 g, 94% yield). The product was characterized by 1H NMR (400 MHz, CDCl3), 13C NMR (101 MHz, CDCl3) and HRMS (ESI/TOF), and the data were consistent with the expected structure.

References

[1] RSC Advances, 2018, vol. 8, # 25, p. 13755 - 13763
[2] Synthetic Communications, 2018, vol. 48, # 6, p. 626 - 631
[3] Patent: WO2011/112186, 2011, A1. Location in patent: Page/Page column 202
[4] Patent: CN108530315, 2018, A. Location in patent: Paragraph 0100-0102
[5] Journal of Heterocyclic Chemistry, 2007, vol. 44, # 6, p. 1383 - 1387

Ethyl O-mesitylsulfonylacetohydroxamate Preparation Products And Raw materials

Raw materials

Preparation Products

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Ethyl O-mesitylsulfonylacetohydroxamate Suppliers

Matrix Fine Chemicals GmbH
Tel
--
Fax
--
Email
nfo@matrix-fine-chemicals.com
Country
Switzerland
ProdList
6968
Advantage
58
SIGMA-RBI
Tel
--
Fax
--
Country
Switzerland
ProdList
6896
Advantage
91
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View Lastest Price from Ethyl O-mesitylsulfonylacetohydroxamate manufacturers

ZHENGZHOU JIUYI TIME NEW MATERIALS CO,.LTD
Product
Ethyl N-[(mesitylsulfonyl)oxy]ethanimidate 38202-27-6
Price
US $2.20-8.80/kg
Min. Order
1kg
Purity
99%min
Supply Ability
100kg
Release date
2025-09-08
Career Henan Chemical Co
Product
Ethyl O-mesitylsulfonylacetohydroxamate 38202-27-6
Price
US $1.00/KG
Min. Order
1KG
Purity
≥98%
Supply Ability
200KG
Release date
2019-08-30

38202-27-6, Ethyl O-mesitylsulfonylacetohydroxamateRelated Search:


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  • 38202-27-6
  • 246CH33C6H2SO2ONCCH3OC2H5
  • C13H19NO4S
  • Sulfur Compounds (for Synthesis)
  • Amination
  • Building Blocks
  • Sulfonates/Sulfinates
  • Sulfur Compounds
  • Organic Building Blocks
  • Building Blocks
  • Chemical Synthesis
  • Organic Building Blocks
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  • Sulfur Compounds
  • Amination
  • Sulfur Compounds (for Synthesis)
  • Synthetic Organic Chemistry