4746-97-8 | 1,4-Cyclohexanedione monoethylene ketal

Packsize	Purity	Availability	Price	Discounted Price
1g	99%	in stock	$6.00	$4.00
5g	99%	in stock	$8.00	$5.00
10g	99%	in stock	$9.00	$6.00
25g	99%	in stock	$12.00	$8.00
100g	99%	in stock	$30.00	$21.00
500g	99%	in stock	$149.00	$104.00

Description

• Catalog Number: AB43169
• Chemical Name: 1,4-Cyclohexanedione monoethylene ketal
• CAS Number: 4746-97-8
• Molecular Formula: C8H12O3
• Molecular Weight: 156.1791
• MDL Number: MFCD00010214
• SMILES: O=C1CCC2(CC1)OCCO2

Computed Properties

• Complexity: 158
• Covalently-Bonded Unit Count: 1
• Heavy Atom Count: 11
• Hydrogen Bond Acceptor Count: 3
• XLogP3: -0.1

Literature

• 13,13-Dimethyl-des-C,D analogues of (20S)-1α,25-dihydroxy-2-methylene-19-norvitamin D₃ (2MD): total synthesis, docking to the VDR, and biological evaluation.

  Bioorganic & medicinal chemistry 20111201

• Synthesis and SAR studies of 1,4-benzoxazine MenB inhibitors: novel antibacterial agents against Mycobacterium tuberculosis.

  Bioorganic & medicinal chemistry letters 20101101

• 1-desoxy analog of 2MD: synthesis and biological activity of (20S)-25-hydroxy-2-methylene-19-norvitamin D3.

  The Journal of steroid biochemistry and molecular biology 20100701

• Enantio- and diastereoselective total synthesis of (+)-panepophenanthrin, a ubiquitin-activating enzyme inhibitor, and biological properties of its new derivatives.

  Chemistry, an Asian journal 20061218

• Studies on a total synthesis of the microbial immunosuppresive agent FR901483.

  The Journal of organic chemistry 20060303

• pi-Facial stereoselectivity in Diels-Alder cycloadditions to 1-oxaspiro[4.5]deca-6,9-dien-8-one. The strong directive effect of ether oxygen in a cross-conjugated ketone setting.

  Organic letters 20030724

• Aromatization of 1,6,7,7a-tetrahydro-2H-indol-2-ones by a novel process. Preparation of key-intermediate methyl 1-benzyl-5-methoxy-1H-indole-3-acetate and the syntheses of serotonin, melatonin, and bufotenin.

  The Journal of organic chemistry 20020405