Name: Name:Ethylenesulfate
Brand: AABLOCKS
SKU: AA0037VT
Rating: 90 (10 reviews)

1,3,2-Dioxathiolane 2,2-dioxide serves as a valuable precursor in the synthesis of imidazolidinium salts. This compound finds utility in organic chemistry reactions where it facilitates the formation of imidazolidinium salts, which have various applications in pharmaceuticals, materials science, and organic synthesis. Its role in these reactions highlights its significance as a versatile building block in the creation of diverse chemical compounds.

Catalog No.: AA0037VT

1072-53-3 | Ethylenesulfate

Pack Size： 5g

Purity： 97%

in stock

$18.00 $13.00

Pack Size： 25g

Purity： 97%

in stock

$34.00 $24.00

Pack Size： 100g

Purity： 98%

in stock

$75.00 $53.00

Pack Size： 500g

Purity： 98%

in stock

$250.00 $175.00

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Technical Information

Catalog Number: AA0037VT

Chemical Name: Ethylenesulfate

CAS Number: 1072-53-3

Molecular Formula: C2H4O4S

Molecular Weight: 124.1158

MDL Number: MFCD00221769

SMILES: O=S1(=O)OCCO1

NSC Number: 526594

Properties

Complexity: 128

Covalently-Bonded Unit Count: 1

Defined Atom Stereocenter Count: 0

Defined Bond Stereocenter Count: 0

Formal Charge: 0

Heavy Atom Count: 7

Hydrogen Bond Acceptor Count: 4

Hydrogen Bond Donor Count: 0

Isotope Atom Count: 0

Rotatable Bond Count: 0

Undefined Atom Stereocenter Count: 0

Undefined Bond Stereocenter Count: 0

XLogP3: -0.5

Upstream Synthesis Route

188290-36-0

1072-53-3

5402-55-1

[1]Synthesis,2008,#11,p.1793-1797

872-31-1

1072-53-3

13781-67-4

[1]Synthesis,2008,#11,p.1793-1797

3741-38-6

1072-53-3

[1]Patent:CN108822073,2018,A,.Locationinpatent:Paragraph0017-0028

[2]Patent:CN106187989,2016,A,.Locationinpatent:Paragraph0016

[3]ActaChemicaScandinavica,1996,vol.50,#2,p.170-177

[4]JournaloftheChemicalSociety,ChemicalCommunications,1983,#23,p.1392-1394

[5]Molecules,2005,vol.10,#9,p.1169-1178

[6]OrganicLetters,2015,vol.17,#23,p.5898-5901

[7]TetrahedronAsymmetry,1994,vol.5,#1,p.83-92

[8]Tetrahedron,1995,vol.51,#17,p.5169-5180

[9]BioorganicandMedicinalChemistryLetters,2010,vol.20,#7,p.2151-2155

107-21-1

1072-53-3

[1]Patent:CN107629032,2018,A,.Locationinpatent:Paragraph0071;0072;0073;0074;0075;0076;0077;0091

[2]TetrahedronLetters,1997,vol.38,#27,p.4841-4844

[3]Patent:CN108409708,2018,A,.Locationinpatent:Paragraph0072;0073;0084;0085;0086;0087

75-21-8

1072-53-3

[1]Patent:CN108658928,2018,A,.Locationinpatent:Paragraph0023;0024;0025;0026;0027;0028;0029;0031

[2]Patent:US5274123,1993,A,

Downstream Synthesis Route

1072-53-3

926-39-6

[1]JournalofHeterocyclicChemistry,1972,vol.9,p.891-894

3741-38-6

1072-53-3

[1]Patent:CN108822073,2018,A.Locationinpatent:Paragraph0017-0028

[2]Patent:CN106187989,2016,A.Locationinpatent:Paragraph0016

[3]Patent:KR102080198,2020,B1.Locationinpatent:Paragraph0111-0114;0131

[4]Patent:CN109485633,2019,A.Locationinpatent:Paragraph0019;0020;0021

[5]ActaChemicaScandinavica,1996,vol.50,p.170-177

[6]JournaloftheChemicalSociety.Chemicalcommunications,1983,p.1392-1394

[7]Molecules,2005,vol.10,p.1169-1178

[8]Patent:CN110386916,2019,A.Locationinpatent:Paragraph0055;0056;0057

[9]OrganicLetters,2015,vol.17,p.5898-5901

[10]TetrahedronAsymmetry,1994,vol.5,p.83-92

[11]Tetrahedron,1995,vol.51,p.5169-5180

[12]BioorganicandMedicinalChemistryLetters,2010,vol.20,p.2151-2155

74-85-1

1072-53-3

[1]TetrahedronLetters,1986,vol.27,p.3971-3974

[2]JournalofOrganicChemistryUSSR(EnglishTranslation),1986,vol.22,p.398-399 ZhurnalOrganicheskoiKhimii,1986,vol.22,p.450-452

107-21-1

1072-53-3

[1]Patent:CN110818674,2020,A.Locationinpatent:Paragraph0017-0019

[2]Patent:CN107629032,2018,A.Locationinpatent:Paragraph0071;0072;0073;0074;0075;0076;0077;0091

[3]TetrahedronLetters,1997,vol.38,p.4841-4844

[4]Patent:CN108409708,2018,A.Locationinpatent:Paragraph0072;0073;0084;0085;0086;0087

[5]Patent:CN109776487,2019,A.Locationinpatent:Paragraph0020-0025;0029-0037

6964-21-2

1072-53-3

524937-66-4

[1]JournaloftheAmericanChemicalSociety,2003,vol.125,p.4050-4051

[2]JournaloftheAmericanChemicalSociety,2011,vol.133,p.13872-13875

Application fold

1,3,2-Dioxathiolane 2,2-dioxide serves as a valuable precursor in the synthesis of imidazolidinium salts. This compound finds utility in organic chemistry reactions where it facilitates the formation of imidazolidinium salts, which have various applications in pharmaceuticals, materials science, and organic synthesis. Its role in these reactions highlights its significance as a versatile building block in the creation of diverse chemical compounds.

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