Sign In to View Organizational & Contract Pricing.
Select a Size
About This Item
Linear Formula:
(CH3)3OCO(CH2)2CO2H
CAS Number:
Molecular Weight:
174.19
NACRES:
NA.22
PubChem Substance ID:
UNSPSC Code:
12352100
MDL number:
Assay:
97%
assay
97%
InChI
1S/C8H14O4/c1-8(2,3)12-7(11)5-4-6(9)10/h4-5H2,1-3H3,(H,9,10)
SMILES string
CC(C)(C)OC(=O)CCC(O)=O
InChI key
PCOCFIOYWNCGBM-UHFFFAOYSA-N
mp
51-54 °C (lit.)
functional group
carboxylic acid, ester
Quality Level
Related Categories
General description
mono-tert-Butyl succinate can be prepared by refluxing a mixture of succinic anhydride and N-hydroxyl succinimide in the presence of dimethylaminopyridine and triethylamine in tert-butanol and toluene.
Application
mono-tert-Butyl succinate may be used in the preparation of:
- N-succinyl-L,L-diaminopimelic acid (SDAP)
- H3K9TSu (histone H3 lysine 9 thiosuccinyl) peptide
- tert-butyl 4-oxo-4-(4-tritylpiperazin-1-yl)butanoate
signalword
Warning
hcodes
Hazard Classifications
Eye Irrit. 2 - Skin Irrit. 2 - STOT SE 3
target_organs
Respiratory system
Storage Class
11 - Combustible Solids
wgk
WGK 3
flash_point_f
230.0 °F - closed cup
flash_point_c
110 °C - closed cup
ppe
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.
Zinc-selective inhibition of the promiscuous bacterial amide-hydrolase DapE: implications of metal heterogeneity for evolution and antibiotic drug design.
Uda NR, et al.
Metallomics : Integrated Biometal Science, 6(1), 88-95 (2014)
Bin He et al.
Journal of the American Chemical Society, 134(4), 1922-1925 (2012-01-24)
Sirtuins, a class of enzymes known as nicotinamide adenine dinucleotide-dependent deacetylases, have been shown to regulate a variety of biological processes, including aging, transcription, and metabolism. Sirtuins are considered promising targets for treating several human diseases. There are seven sirtuins
Ying Li et al.
American journal of nuclear medicine and molecular imaging, 3(1), 44-56 (2013-01-24)
Arylboronates capture aqueous (18)F-fluoride in one step to afford a highly polar (18)F-labeled aryltrifluoroborate anion ((18)F-ArBF(3) (-)) that clears rapidly in vivo. To date however, there is little data to show that a ligand labeled with a prosthetic (18)F-ArBF(3) (-)
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