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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

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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

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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

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Certificates of Analysis (COA)

Lot/Batch Number
BCCB9122
BCBP3771V
1451854V
1451854
1323838

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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
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)

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