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515981

Sigma-Aldrich

1,3-Cycloheptanedione

97%

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1 G
¥7,490

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1 G
¥7,490

About This Item

Linear Formula:
C7H10(=O)2
CAS Number:
1194-18-9
Molecular Weight:
126.15
MDL number:
MFCD01863735
UNSPSC Code:
12352100
PubChem Substance ID:
24873858
NACRES:
NA.22

¥7,490

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Quality Level

100

Assay

97%

refractive index

n20/D 1.483 (lit.)

bp

254 °C (lit.)

density

1.1 g/mL at 25 °C (lit.)

functional group

ketone

SMILES string

O=C1CCCCC(=O)C1

InChI

1S/C7H10O2/c8-6-3-1-2-4-7(9)5-6/h1-5H2

InChI key

DBOVMTXPZWVYAQ-UHFFFAOYSA-N

Related Categories

Storage Class Code

10 - Combustible liquids

WGK

WGK 3

Flash Point(F)

Not applicable

Flash Point(C)

Not applicable

Personal Protective Equipment

dust mask type N95 (US), Eyeshields, Gloves

Regulatory Listings

Regulatory Listings are mainly provided for chemical products. Only limited information can be provided here for non-chemical products. No entry means none of the components are listed. It is the user’s obligation to ensure the safe and legal use of the product.

JAN Code

515981-BULK:
515981-VAR:
515981-1G:

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Certificates of Analysis (COA)

Lot/Batch Number
MKCP3870
MKBH1162V
MKBC7493
21998MJ
04918HJ

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Methylation of 1, 3-cyclopentanedione, 1, 3-cyclohexanedione, and 1, 3-cycloheptanedione with iodomethane in aprotic solvents in the absence and in the presence of 18-crown-6.
Sraga J and Hrnciar P.
Chemical Papers, 35(1), 119-126 (1981)
Allen Y Hong et al.
Tetrahedron, 67(52), 10234-10248 (2012-02-22)
General catalytic asymmetric routes toward cyclopentanoid and cycloheptanoid core structures embedded in numerous natural products have been developed. The central stereoselective transformation in our divergent strategies is the enantioselective decarboxylative alkylation of seven-membered β-ketoesters to form α-quaternary vinylogous esters. Recognition
Michael additions of 1, 3-cycloalkanediones to dimethyl acety-lenedicarboxylate.
Hrnciar P, et al.
Chemical Papers, 43(1), 87-95 (1989)
Evan A Sims et al.
Tetrahedron letters, 52(16), 1871-1873 (2011-06-29)
We report the large-scale synthesis of 1,3-cyclooctanedione in five steps with 29% yield. This molecule is a synthetic precurser to difluorinated cyclooctyne, which participates in a bioorthogonal copper-free click reaction with azides. The final step demonstrates the first successful application
Michael addition of 1, 3-cyclopentanedione, 1, 3-cyclohexanedione and 1, 3-cycloheptanedione to 1-(X-phenyl)-2-nitroethylenes.
Hrnciar P and Culak I.
Collection of Czechoslovak Chemical Communications, 49(6), 1421-1431 (1984)

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