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108-22-5,MFCD08669885
Catalog No.:AA0034ZA

108-22-5 | Prop-1-en-2-yl acetate

Pack Size
Purity
Availability
Price(USD)
Quantity
  
25g
98%(GC)
in stock  
$24.00   $17.00
- +
  • Technical Information
  • Properties
  • Literature
  • Request for Quotation
  • Download SDS
Technical Information
Catalog Number:
AA0034ZA
Chemical Name:
Prop-1-en-2-yl acetate
CAS Number:
108-22-5
Molecular Formula:
C5H8O2
Molecular Weight:
100.1158
MDL Number:
MFCD08669885
SMILES:
CC(=C)OC(=O)C
FEMA Number:
4152
UN Number:
2403
Properties
Properties
 
BP:
97.0°C  
Form:
Liquid  
MP:
-93 °C  
Refractive Index:
n20/D 1.401(lit.)  
Solubility:
34g/l  
Storage:
Room Temperature;  

Computed Properties
 
Complexity:
94.3  
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:
2  
Hydrogen Bond Donor Count:
0  
Isotope Atom Count:
0  
Rotatable Bond Count:
2  
Undefined Atom Stereocenter Count:
0  
Undefined Bond Stereocenter Count:
0  
XLogP3:
1  

Literature

Title: Theoretical determination of the infrared spectra of amorphous polymers.

Journal: The journal of physical chemistry. A 20120712

Title: 5-(2-Chloro-benz-yl)-4,5,6,7-tetra-hydro-thieno[3,2-c]pyridin-2-yl acetate.

Journal: Acta crystallographica. Section E, Structure reports online 20120401

Title: Acylation of Chiral Alcohols: A Simple Procedure for Chiral GC Analysis.

Journal: Journal of analytical methods in chemistry 20120101

Title: Direct synthesis of anti-1,3-diols through nonclassical reaction of aryl Grignard reagents with isopropenyl acetate.

Journal: Organic letters 20110121

Title: Mechanism of acetaldehyde-induced deactivation of microbial lipases.

Journal: BMC biochemistry 20110101

Title: Large nonstatistical branching ratio in the dissociation of pentane-2,4-dione radical cation: an ab initio direct classical trajectory study.

Journal: The journal of physical chemistry. A 20090226

Title: Inhibitory effect of some acetyl esters and acetamides on glycation of the histone H1.

Journal: Zeitschrift fur Naturforschung. C, Journal of biosciences 20080101

Title: Enol esters: versatile substrates for Mannich-type multicomponent reactions.

Journal: Organic letters 20071011

Title: Air-stable racemization catalysts for the dynamic kinetic resolution of secondary alcohols.

Journal: The Journal of organic chemistry 20070831

Title: Dynamic kinetic resolution of secondary alcohols combining enzyme-catalyzed transesterification and zeolite-catalyzed racemization.

Journal: Chemistry (Weinheim an der Bergstrasse, Germany) 20070101

Title: The allosteric modulation of lipases and its possible biological relevance.

Journal: Theoretical biology & medical modelling 20070101

Title: Large-scale ruthenium- and enzyme-catalyzed dynamic kinetic resolution of (rac)-1-phenylethanol.

Journal: Beilstein journal of organic chemistry 20070101

Title: One-Pot synthesis of gamma,delta-unsaturated carbonyl compounds from allyl alcohols and vinyl or isopropenyl acetates catalyzed by [IrCl(cod)]2.

Journal: The Journal of organic chemistry 20060804

Title: Application and comparison of immobilized and coated amylose tris-(3,5-dimethylphenylcarbamate) chiral stationary phases for the enantioselective separation of beta-blockers enantiomers by liquid chromatography.

Journal: Talanta 20060115

Title: Stereochemistry of a diastereoisomeric amphiphile and the species of the lipase influence enzyme activity in the transesterification catalyzed by a lipase-co-lyophilizate with the amphiphile in organic media.

Journal: Biotechnology letters 20031101

Title: Efficient lipase-catalyzed enantioselective desymmetrization of prochiral 2,2-disubstituted 1,3-propanediols and meso 1,2-diols using 1-ethoxyvinyl 2-furoate.

Journal: The Journal of organic chemistry 20020125

Title: Lipase-catalyzed irreversible transesterification of 1-(2-furyl)ethanol using isopropenyl acetate.

Journal: Chirality 20010201

Title: Acetyl phosphate synthesis by reaction of isopropenyl acetate and phosphoric acid.

Journal: The Journal of biological chemistry 19500801

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Tags:108-22-5 Molecular Formula|108-22-5 MDL|108-22-5 SMILES|108-22-5 Prop-1-en-2-yl acetate
Catalog No.: AA0034ZA
108-22-5,MFCD08669885
108-22-5 | Prop-1-en-2-yl acetate
Pack Size： 25g
Purity： 98%(GC)
in stock
$24.00 $17.00
Quantity
- +
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Technical Information
Catalog Number: AA0034ZA
Chemical Name: Prop-1-en-2-yl acetate
CAS Number: 108-22-5
Molecular Formula: C5H8O2
Molecular Weight: 100.1158
MDL Number: MFCD08669885
SMILES: CC(=C)OC(=O)C
FEMA Number: 4152
UN Number: 2403
Properties
BP: 97.0°C  
Form: Liquid  
MP: -93 °C  
Refractive Index: n20/D 1.401(lit.)  
Solubility: 34g/l  
Storage: Room Temperature;  
Complexity: 94.3  
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: 2  
Hydrogen Bond Donor Count: 0  
Isotope Atom Count: 0  
Rotatable Bond Count: 2  
Undefined Atom Stereocenter Count: 0  
Undefined Bond Stereocenter Count: 0  
XLogP3: 1  
Literature fold

Title: Theoretical determination of the infrared spectra of amorphous polymers.

Journal: The journal of physical chemistry. A20120712

Title: 5-(2-Chloro-benz-yl)-4,5,6,7-tetra-hydro-thieno[3,2-c]pyridin-2-yl acetate.

Journal: Acta crystallographica. Section E, Structure reports online20120401

Title: Acylation of Chiral Alcohols: A Simple Procedure for Chiral GC Analysis.

Journal: Journal of analytical methods in chemistry20120101

Title: Direct synthesis of anti-1,3-diols through nonclassical reaction of aryl Grignard reagents with isopropenyl acetate.

Journal: Organic letters20110121

Title: Mechanism of acetaldehyde-induced deactivation of microbial lipases.

Journal: BMC biochemistry20110101

Title: Large nonstatistical branching ratio in the dissociation of pentane-2,4-dione radical cation: an ab initio direct classical trajectory study.

Journal: The journal of physical chemistry. A20090226

Title: Inhibitory effect of some acetyl esters and acetamides on glycation of the histone H1.

Journal: Zeitschrift fur Naturforschung. C, Journal of biosciences20080101

Title: Enol esters: versatile substrates for Mannich-type multicomponent reactions.

Journal: Organic letters20071011

Title: Air-stable racemization catalysts for the dynamic kinetic resolution of secondary alcohols.

Journal: The Journal of organic chemistry20070831

Title: Dynamic kinetic resolution of secondary alcohols combining enzyme-catalyzed transesterification and zeolite-catalyzed racemization.

Journal: Chemistry (Weinheim an der Bergstrasse, Germany)20070101

Title: The allosteric modulation of lipases and its possible biological relevance.

Journal: Theoretical biology & medical modelling20070101

Title: Large-scale ruthenium- and enzyme-catalyzed dynamic kinetic resolution of (rac)-1-phenylethanol.

Journal: Beilstein journal of organic chemistry20070101

Title: One-Pot synthesis of gamma,delta-unsaturated carbonyl compounds from allyl alcohols and vinyl or isopropenyl acetates catalyzed by [IrCl(cod)]2.

Journal: The Journal of organic chemistry20060804

Title: Application and comparison of immobilized and coated amylose tris-(3,5-dimethylphenylcarbamate) chiral stationary phases for the enantioselective separation of beta-blockers enantiomers by liquid chromatography.

Journal: Talanta20060115

Title: Stereochemistry of a diastereoisomeric amphiphile and the species of the lipase influence enzyme activity in the transesterification catalyzed by a lipase-co-lyophilizate with the amphiphile in organic media.

Journal: Biotechnology letters20031101

Title: Efficient lipase-catalyzed enantioselective desymmetrization of prochiral 2,2-disubstituted 1,3-propanediols and meso 1,2-diols using 1-ethoxyvinyl 2-furoate.

Journal: The Journal of organic chemistry20020125

Title: Lipase-catalyzed irreversible transesterification of 1-(2-furyl)ethanol using isopropenyl acetate.

Journal: Chirality20010201

Title: Acetyl phosphate synthesis by reaction of isopropenyl acetate and phosphoric acid.

Journal: The Journal of biological chemistry19500801

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