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820-71-3,MFCD00048215
Catalog No.:AA003HJD
820-71-3 | 2-Methyl-2-propenyl Acetate , 98%
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1g
97%
in stock  
$25.00
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5g
97%
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$60.00
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10g
97%
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$117.00
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25g
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$145.00
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  • Technical Information
  • Properties
  • Literature
  • Request for Quotation
  • Technical Information
  • Properties
  • Literature
Technical Information
Catalog Number:
AA003HJD
Chemical Name:
2-Methyl-2-propenyl Acetate , 98%
CAS Number:
820-71-3
Molecular Formula:
C6H10O2
Molecular Weight:
114.1424
MDL Number:
MFCD00048215
IUPAC Name:
2-methylprop-2-enyl acetate
InChI:
InChI=1S/C6H10O2/c1-5(2)4-8-6(3)7/h1,4H2,2-3H3
InChI Key:
IVKYUXHYUAMPMT-UHFFFAOYSA-N
SMILES:
CC(=O)OCC(=C)C
EC Number:
212-471-1
Properties
Computed Properties
 
Complexity:
105  
Compound Is Canonicalized:
Yes
Covalently-Bonded Unit Count:
1  
Defined Atom Stereocenter Count:
0
Defined Bond Stereocenter Count:
0
Exact Mass:
114.068g/mol
Formal Charge:
0
Heavy Atom Count:
8  
Hydrogen Bond Acceptor Count:
2  
Hydrogen Bond Donor Count:
0
Isotope Atom Count:
0
Molecular Weight:
114.144g/mol
Monoisotopic Mass:
114.068g/mol
Rotatable Bond Count:
3  
Topological Polar Surface Area:
26.3A^2
Undefined Atom Stereocenter Count:
0
Undefined Bond Stereocenter Count:
0
XLogP3:
1.4  

Synonyms
 
Methallyl acetate 
2-Methylallyl acetate 
AI3-02670 
.beta.-Methallyl acetate 
2-methylprop-2-enyl acetate 
1-Acetoxy-2-methyl-2-propene 
AC1L2D25 
AC1Q62L6 
SCHEMBL1034236 
Acetic acid, 2-methylallylester 
2-Methyl-2-propenyl acetate # 
Acetic Acid 2-Methylallyl Ester 
820-71-3 
CTK5E9385 
Acetic acid 2-methyl-2-propenyl 
DTXSID20231511 
ALBB-015064 
ZINC1845661 
ZX-AN013772 
ANW-37494 
MFCD00048215 
2-Methyl-2-propenyl Acetate , 98% 
AKOS005175057 
2-methylprop-2-en-1-yl acetate 
FCH2070960 
RL05132 
2-Propen-1-ol,2-methyl-, 1-acetate 
Acetic Acid 2-Methyl-2-propenyl Ester 
AN-47671 
CJ-30114 
DA-17492 
M643 
AB0015319 
TR-032361 
2-Methyl-2-propenyl acetate 
FT-0683953 
R1797 
820M713 
C-00546 
J-521689 
I14-26721 
Methallylacetate 
C6H10O2 
CID69962 
AR-1E4127 
2-Propen-1-ol, 2-methyl-, acetate 
C6-H10-O2 
A1605 
86710-23-8 
IVKYUXHYUAMPMT-UHFFFAOYSA-N 
EINECS 212-471-1 
beta-Methallyl acetate 
ACMC-209pmw 
Literature

Title: Catalytic enantioselective Grignard Nozaki-Hiyama methallylation from the alcohol oxidation level: chloride compensates for π-complex instability.

Journal: Chemical communications (Cambridge, England) 20110928

Title: Nitrogen-directed ortho-selective homocoupling of aromatic compounds catalyzed by ruthenium complexes.

Journal: Organic letters 20080501

Title: Inter- and intramolecular palladium-catalyzed allyl cross-coupling reactions using allylindium generated in situ from allyl acetates, indium, and indium trichloride.

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

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