Home Other Building Blocks Ethyl 2-butynoate

Ethyl 2-butynoate

CAS No.:
4341-76-8
Catalog Number:
AG003790
Molecular Formula:
C6H8O2
Molecular Weight:
112.1265
Pack Size
Purity
Availability
Location
Price(USD)
Quantity
  
1g
95%
In Stock USA
United States
$13
- +
5g
98%
In Stock USA
United States
$37
- +
25g
98%
In Stock USA
United States
$144
- +
100g
98%
In Stock USA
United States
$444
- +
500g
98%
In Stock USA
United States
$1563
- +
Product Description
Catalog Number:
AG003790
Chemical Name:
Ethyl 2-butynoate
CAS Number:
4341-76-8
Molecular Formula:
C6H8O2
Molecular Weight:
112.1265
MDL Number:
MFCD00015182
IUPAC Name:
ethyl but-2-ynoate
InChI:
InChI=1S/C6H8O2/c1-3-5-6(7)8-4-2/h4H2,1-2H3
InChI Key:
FCJJZKCJURDYNF-UHFFFAOYSA-N
SMILES:
CCOC(=O)C#CC
EC Number:
224-395-6
Properties
Complexity:
135  
Compound Is Canonicalized:
Yes
Covalently-Bonded Unit Count:
1  
Defined Atom Stereocenter Count:
0
Defined Bond Stereocenter Count:
0
Exact Mass:
112.052g/mol
Formal Charge:
0
Heavy Atom Count:
8  
Hydrogen Bond Acceptor Count:
2  
Hydrogen Bond Donor Count:
0
Isotope Atom Count:
0
Molecular Weight:
112.128g/mol
Monoisotopic Mass:
112.052g/mol
Rotatable Bond Count:
2  
Topological Polar Surface Area:
26.3A^2
Undefined Atom Stereocenter Count:
0
Undefined Bond Stereocenter Count:
0
XLogP3:
1.5  
Literature
Title Journal
Calyculins and related marine natural products as serine-threonine protein phosphatase PP1 and PP2A inhibitors and total syntheses of calyculin A, B, and C. Marine drugs 20100101
Isolation and crystal structures of both enol and keto tautomer intermediates in a hydration of an alkyne-carboxylic acid ester catalyzed by iridium complexes in water. Journal of the American Chemical Society 20081217
Increases in microbial nitrogen production and efficiency in vitro with three inhibitors of ruminal methanogenesis. Canadian journal of microbiology 20070401
Effects of butyrate precursors on electron relocation when methanogenesis is inhibited in ruminal mixed cultures. Letters in applied microbiology 20060601
Synthesis of carbocyclic hydantocidins via regioselective and diastereoselective phosphine-catalyzed [3 + 2]-cycloadditions to 5-methylenehydantoins. The Journal of organic chemistry 20050805
Effects of several inhibitors on pure cultures of ruminal methanogens. Journal of applied microbiology 20040101
Use of some novel alternative electron sinks to inhibit ruminal methanogenesis. Reproduction, nutrition, development 20030101
Properties