Skip to Content
Merck
CN

178241

Isobutyl 1,2-dihydro-2-isobutoxy-1-quinolinecarboxylate

99%

Synonym(s):

1-Isobutoxycarbonyl-2-isobutoxy-1,2-dihydroquinoline, 2-Isobutoxy-1-isobutoxycarbonyl-1,2-dihydroquinoline, IIDQ

Sign In to View Organizational & Contract Pricing.

Select a Size

About This Item

Empirical Formula (Hill Notation):
C18H25NO3
CAS Number:
38428-14-7
Molecular Weight:
303.40
UNSPSC Code:
12352005
NACRES:
NA.22
PubChem Substance ID:
24850726
MDL number:
MFCD00006702
Beilstein/REAXYS Number:
1543065

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

100

InChI

1S/C18H25NO3/c1-13(2)11-21-17-10-9-15-7-5-6-8-16(15)19(17)18(20)22-12-14(3)4/h5-10,13-14,17H,11-12H2,1-4H3

SMILES string

CC(C)COC1C=Cc2ccccc2N1C(=O)OCC(C)C

InChI key

LPBHYOYZZIFCQT-UHFFFAOYSA-N

assay

99%

reaction suitability

reaction type: Coupling Reactions

refractive index

n20/D 1.523 (lit.)

bp

140-142 °C/0.2 mmHg (lit.)

density

1.022 g/mL at 25 °C (lit.)

application(s)

peptide synthesis

functional group

ether

Related Categories

pictograms

Health hazard
GHS08

signalword

Danger

hcodes

H341,H350

Hazard Classifications

Carc. 1B - Muta. 2

Storage Class

6.1C - Combustible acute toxic Cat.3 / toxic compounds or compounds which causing chronic effects

wgk

WGK 3

flash_point_f

235.4 °F - closed cup

flash_point_c

113 °C - closed cup

ppe

Eyeshields, Gloves

Choose from one of the most recent versions:

Certificates of Analysis (COA)

Lot/Batch Number
BCCB9122
BCBP3771V
1451854V
1451854
1323838

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

Effect of hydrophobic carboxyl reagents on the proton flux through coupling factor CF0 in thylakoid membrane.
Y Ho et al.
Biochemistry, 19(12), 2650-2655 (1980-06-10)
Manisha Sathe et al.
Bioorganic & medicinal chemistry letters, 20(5), 1792-1795 (2010-02-05)
Polystyrene-supported 2-isobutoxy-1-isobutoxycarbonyl-1,2-dihydroquinoline (PS-IIDQ), a polymer-supported covalent coupling reagent, was successfully employed for the first time in the bioconjugation of an example hapten (phytanic acid derivative) to a carrier protein (bovine serum albumin (BSA)) within the context of immunogen preparation for

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