1072-72-6 | Tetrahydro-4H-thiopyran-4-one

Packsize	Purity	Availability	Price	Discounted Price
5g	98%	in stock	$7.00	$5.00
10g	98%	in stock	$12.00	$8.00
25g	98%	in stock	$21.00	$15.00
100g	98%	in stock	$80.00	$56.00
500g	98%	in stock	$396.00	$277.00

Description

• Catalog Number: AB79557
• Chemical Name: Tetrahydro-4H-thiopyran-4-one
• CAS Number: 1072-72-6
• Molecular Formula: C5H8OS
• Molecular Weight: 116.1814
• MDL Number: MFCD00006660
• SMILES: O=C1CCSCC1
• NSC Number: 41599

Computed Properties

• Complexity: 72.1
• Covalently-Bonded Unit Count: 1
• Heavy Atom Count: 7
• Hydrogen Bond Acceptor Count: 2
• XLogP3: 0.3

Literature

• BDMC33, A curcumin derivative suppresses inflammatory responses in macrophage-like cellular system: role of inhibition in NF-κB and MAPK signaling pathways.

  International journal of molecular sciences 20120101

• 5-(4-Chloro-phen-yl)-1-methyl-3-phenyl-3,6,8,9-tetra-hydro-pyrazolo-[3,4-b]thio-pyrano[4,3-d]pyridine.

  Acta crystallographica. Section E, Structure reports online 20110901

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

  Bioorganic & medicinal chemistry letters 20101101

• (S)-3-[(S,E)-4-(4-Chloro-phen-yl)-1-nitro-but-3-en-2-yl]thian-4-one.

  Acta crystallographica. Section E, Structure reports online 20091101

• Efficient method for the synthesis of pyranoquinoline, thiopyranoquinoline, thienoquinoline, and naphtho[2,7]naphthyridine derivatives catalyzed by iodine.

  Journal of combinatorial chemistry 20090101

• The thiopyran route to polypropionates: enantioselective synthesis of membrenone B from racemic fragments.

  The Journal of organic chemistry 20070928

• Thiopyran route to polypropionates: an efficient synthesis of serricornin.

  The Journal of organic chemistry 20061110

• Asymmetric synthesis of hexapropionate synthons by sequential enantiotopic group selective enolization of meso diketones.

  Organic letters 20060608

• A comparison of cyclohexanone and tetrahydro-4H-thiopyran-4-one 1,1-dioxide as pharmacophores for the design of peptide-based inhibitors of the serine protease plasmin.

  The Journal of organic chemistry 20051014

• Syn-anti isomerization of aldols by enolization.

  The Journal of organic chemistry 20040709

• Influence of the beta-alkoxy group on the diastereoselectivity of Aldol reactions of tetrahydro-4H-thiopyran-4-one with 4-Alkoxytetrahydro-2H-thiopyran-3-carboxaldehydes.

  The Journal of organic chemistry 20020308

• Carbanion-induced base-catalyzed synthesis of 1H-isothiochromenes, benzo[c]thiochromenes through ring-transformation reactions of 6-aryl-2H-pyran-2-ones.

  The Journal of organic chemistry 20010810