Skip to Content
Merck
CN

254487

Di-tert-butyl malonate

98%

Synonym(s):

1,3-Bis(1,1-dimethylethyl) propanedioate, 1,3-Di-tert-butyl propanedioate, Bis(1,1-dimethylethyl) malonate, di-tert-butyl propanedioate, tert-Butyl malonate

Sign In to View Organizational & Contract Pricing

Select a Size

About This Item

Linear Formula:
(CH3)3COCOCH2COOC(CH3)3
CAS Number:
541-16-2
Molecular Weight:
216.27
Beilstein:
1781766
EC Number:
208-769-6
MDL number:
MFCD00008810
UNSPSC Code:
12352100
PubChem Substance ID:
24855386
NACRES:
NA.22

Key Documents

View All Documentation
Technical Service
Need help? Our team of experienced scientists is here for you.
Let Us Assist
Technical Service
Need help? Our team of experienced scientists is here for you.
Let Us Assist

Quality Level

200

Assay

98%

form

liquid

refractive index

n20/D 1.418 (lit.)

bp

110-111 °C/22 mmHg (lit.)

mp

−7-−6 °C (lit.)

density

0.966 g/mL at 25 °C (lit.)

functional group

ester

SMILES string

CC(C)(C)OC(=O)CC(=O)OC(C)(C)C

InChI

1S/C11H20O4/c1-10(2,3)14-8(12)7-9(13)15-11(4,5)6/h7H2,1-6H3

InChI key

CLPHAYNBNTVRDI-UHFFFAOYSA-N

Looking for similar products? Visit Product Comparison Guide

Related Categories

Application

Di-tert-butyl malonate was used in total synthesis of (+/−)-actinophyllic acid. It was also employed as precursor for metal-organic chemical vapor deposition of HfO2 and ZrO2 thin films.

Storage Class Code

10 - Combustible liquids

WGK

WGK 3

Flash Point(F)

192.2 °F - closed cup

Flash Point(C)

89 °C - closed cup

Personal Protective Equipment

dust mask type N95 (US), Eyeshields, Gloves

Regulatory Information

新产品
This item has

Choose from one of the most recent versions:

Certificates of Analysis (COA)

Lot/Batch Number
BCBT2438
BCBJ3840V
BCBB1870V
BCBB1870
1389779

Don't see the Right Version?

If you require a particular version, you can look up a specific certificate by the Lot or Batch number.

Search for a COA

Already Own This Product?

Find documentation for the products that you have recently purchased in the Document Library.

Visit the Document Library

Connor L Martin et al.
Journal of the American Chemical Society, 132(13), 4894-4906 (2010-03-12)
Development of efficient sequences for the total syntheses of (+/-)-actinophyllic acid (rac-1) and (-)-actinophyllic acid (1) are described. The central step in these syntheses is the aza-Cope/Mannich reaction, which constructs the previously unknown hexacyclic ring system of actinophyllic acid in
Ramasamy Pothiraja et al.
Dalton transactions (Cambridge, England : 2003), (4)(4), 654-663 (2009-04-22)
New Hf and Zr malonate complexes have been synthesized by the reaction of metal amides with different malonate ligands (L = dimethyl malonate (Hdmml), diethyl malonate (Hdeml), di-tert-butyl malonate (Hdbml) and bis(trimethylsilyl) malonate (Hbsml)). Homoleptic eight-coordinated monomeric compounds of the

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