537594
tert-Butyl acetoacetate
reagent grade, 98%
Synonym(s):
TBAA
Sign Into View Organizational & Contract Pricing
All Photos(1)
About This Item
Recommended Products
grade
reagent grade
Quality Level
Assay
98%
expl. lim.
8 % (lit.)
impurities
≤0.20% water
water
refractive index
n20/D 1.419 (lit.)
bp
71-72 °C/11 mmHg (lit.)
mp
-38 °C (lit.)
density
0.954 g/mL at 25 °C (lit.)
functional group
ester
ketone
SMILES string
CC(=O)CC(=O)OC(C)(C)C
InChI
1S/C8H14O3/c1-6(9)5-7(10)11-8(2,3)4/h5H2,1-4H3
InChI key
JKUYRAMKJLMYLO-UHFFFAOYSA-N
Looking for similar products? Visit Product Comparison Guide
General description
tert-Butyl acetoacetate (t-BAA) is a cheap and easy to store commercial reagent. Reaction demonstrated that the more hindered tert-butyl acetoacetate (t-BAA, la) is ca.15-20-fold more reactive than the more commonly used methyl or ethyl analogs. It is widely employed as an acetoacetylating reagent.
Application
tert-Butyl acetoacetate may be used in the synthesis of:
- various acetoacetic acid derivatives
- acetoacetates
- acetoacetamides
- 1-(diethylamino)-2-acetoacetoxypropane
- (S)-tert-butyl 3-hydroxybutyrate
- benzothiazole β-keto ester derivatives
- 3,4-disubstituted pyrroles
Storage Class Code
10 - Combustible liquids
WGK
WGK 1
Flash Point(F)
150.8 °F - closed cup
Flash Point(C)
66 °C - closed cup
Personal Protective Equipment
dust mask type N95 (US), Eyeshields, Gloves
Choose from one of the most recent versions:
Already Own This Product?
Find documentation for the products that you have recently purchased in the Document Library.
Organic & biomolecular chemistry, 11(1), 62-68 (2012-10-17)
Prodigiosenes, possessing a 4-methoxypyrrolyldipyrrin skeleton, are known for their anti-cancer activity. Structural modification of the C-ring resulted in a series of prodigiosenes that displayed promising activity against leukemia cell lines during in vitro analysis against the NCI 60 cancer cell
Transesterification.
Chemical Reviews, 93(4), 1449-1470 (1993)
Transacetoacetylation with tert-butyl acetoacetate: synthetic applications.
The Journal of Organic Chemistry, 56(5), 1713-1718 (1991)
Highly enantioselective Mannich reactions of imines with tert-butyl acetoacetate catalyzed by squaramide organocatalyst.
Tetrahedron Asymmetry, 25(8), 637-643 (2014)
Synthesis of (S)-Tert-Butyl 3-Hydroxybutyrate by Asymmetric Reduction of Tert-Butyl Acetoacetate with Saccharomyces cerevisiae B5.
Advanced Materials Research, 704 (2013)
Our team of scientists has experience in all areas of research including Life Science, Material Science, Chemical Synthesis, Chromatography, Analytical and many others.
Contact Technical Service