Home Other Building Blocks 2-Methyl-3-butyn-2-ol

2-Methyl-3-butyn-2-ol

CAS No.:
115-19-5
Catalog Number:
AG0037XE
Molecular Formula:
C5H8O
Molecular Weight:
84.1164
Pack Size
Purity
Availability
Location
Price(USD)
Quantity
  
5g
95%
In Stock USA
United States
$13
- +
25g
95%
In Stock USA
United States
$19
- +
100g
95%
In Stock USA
United States
$50
- +
500g
95%
In Stock USA
United States
$188
- +
Product Description
Catalog Number:
AG0037XE
Chemical Name:
2-Methyl-3-butyn-2-ol
CAS Number:
115-19-5
Molecular Formula:
C5H8O
Molecular Weight:
84.1164
MDL Number:
MFCD00004467
IUPAC Name:
2-methylbut-3-yn-2-ol
InChI:
InChI=1S/C5H8O/c1-4-5(2,3)6/h1,6H,2-3H3
InChI Key:
CEBKHWWANWSNTI-UHFFFAOYSA-N
SMILES:
C#CC(O)(C)C
EC Number:
204-070-5
UNII:
EHB904XHKH
NSC Number:
523
RTECS Number:
ES0810000
UN Number:
1987
Properties
Complexity:
83.4  
Compound Is Canonicalized:
Yes
Covalently-Bonded Unit Count:
1  
Defined Atom Stereocenter Count:
0
Defined Bond Stereocenter Count:
0
Exact Mass:
84.058g/mol
Formal Charge:
0
Heavy Atom Count:
6  
Hydrogen Bond Acceptor Count:
1  
Hydrogen Bond Donor Count:
1  
Isotope Atom Count:
0
Molecular Weight:
84.118g/mol
Monoisotopic Mass:
84.058g/mol
Rotatable Bond Count:
1  
Topological Polar Surface Area:
20.2A^2
Undefined Atom Stereocenter Count:
0
Undefined Bond Stereocenter Count:
0
XLogP3:
0.3  
Literature
Title Journal
5,8-Bis(3-hy-droxy-3-methyl-but-1-yn-1-yl)-2,11-dithia-[3.3]paracyclo-phane. Acta crystallographica. Section E, Structure reports online 20111201
A computational study on the role of chiral N-oxides in enantioselective Pauson-Khand reactions. Chemistry (Weinheim an der Bergstrasse, Germany) 20110829
Structure sensitivity of alkynol hydrogenation on shape- and size-controlled palladium nanocrystals: which sites are most active and selective? Journal of the American Chemical Society 20110817
Basic reactivity of CaO: investigating active sites under operating conditions. Physical chemistry chemical physics : PCCP 20101128
4,4'-[2,5-Bis(dodec-yloxy)-p-phenyl-ene]bis-(2-methyl-but-3-yn-2-ol). Acta crystallographica. Section E, Structure reports online 20100701
4-(4-Meth-oxy-phen-yl)-2-methyl-but-3-yn-2-ol. Acta crystallographica. Section E, Structure reports online 20100701
9-Isopropenyl-4-methyl-2H-thieno[2,3-h]chromen-2-one. Acta crystallographica. Section E, Structure reports online 20090601
2,2'-Dimethyl-4,4'-(sulfonyldi-p-phenyl-ene)dibut-3-yn-2-ol dihydrate. Acta crystallographica. Section E, Structure reports online 20090201
4-(9-Anthryl)-2-methylbutyn-2-ol. Acta crystallographica. Section E, Structure reports online 20080201
Ligand accelerated indium(III)-catalyzed asymmetric alkynylation of aldehydes with 2-methyl-3-butyn-2-ol as an ethyne equivalent donor. Chemical communications (Cambridge, England) 20070307
Hydride-alkenylcarbyne to alkenylcarbene transformation in bisphosphine-osmium complexes. Journal of the American Chemical Society 20050810
Tandem Sonogashira coupling: an efficient tool for the synthesis of diarylalkynes. Organic letters 20041223
Six- and eightfold palladium-catalyzed cross-coupling reactions of hexa- and octabromoarenes. Chemistry (Weinheim an der Bergstrasse, Germany) 20041217
Regioselective synthesis of 6-alkyl- and 6-prenylpolyhydroxyisoflavones and 6-alkylcoumaronochromone derivatives. Chemical & pharmaceutical bulletin 20041101
Synthesis, X-ray crystal structure and biological properties of acetylenic flavone derivatives. Farmaco (Societa chimica italiana : 1989) 20030901
One step Pd(0)-catalyzed synthesis, X-ray analysis, and photophysical properties of cyclopent[hi]aceanthrylene: fullerene-like properties in a nonalternant cyclopentafused aromatic hydrocarbon. Journal of the American Chemical Society 20020109
Properties