149-73-5 | Trimethyl orthoformate

Packsize	Purity	Availability	Price	Discounted Price
5g	98	in stock	$13.00	$9.00
25g	98	in stock	$19.00	$13.00
100g	98%	in stock	$74.00	$52.00
500g	98%	in stock	$251.00	$176.00

Description

• Catalog Number: AA74108
• Chemical Name: Trimethyl orthoformate
• CAS Number: 149-73-5
• Molecular Formula: C4H10O3
• Molecular Weight: 106.1204
• MDL Number: MFCD00008483
• SMILES: COC(OC)OC
• NSC Number: 147479

Computed Properties

• Complexity: 28.4
• Covalently-Bonded Unit Count: 1
• Heavy Atom Count: 7
• Hydrogen Bond Acceptor Count: 3
• Rotatable Bond Count: 3
• XLogP3: 0.2

Literature

• Identification, design and biological evaluation of bisaryl quinolones targeting Plasmodium falciparum type II NADH:quinone oxidoreductase (PfNDH2).

  Journal of medicinal chemistry 20120308

• Identification, design and biological evaluation of heterocyclic quinolones targeting Plasmodium falciparum type II NADH:quinone oxidoreductase (PfNDH2).

  Journal of medicinal chemistry 20120308

• Tetra-hedral zinc in tetra-kis-(1-methyl-1H-imidazole-κN)zinc bis-(tetra-fluorido-borate).

  Acta crystallographica. Section E, Structure reports online 20120101

• Synthesis and biological activities of a 3'-azido analogue of Doxorubicin against drug-resistant cancer cells.

  International journal of molecular sciences 20120101

• Tetra-μ-acetato-κO:O'-bis-{[N-(4-methyl-phen-yl)pyridin-2-amine-κN]copper(II)}(Cu-Cu).

  Acta crystallographica. Section E, Structure reports online 20111101

• Tetra-μ-acetato-κO:O'-bis-[(2-phen-oxy-pyrimidine-κN)copper(II)](Cu-Cu).

  Acta crystallographica. Section E, Structure reports online 20111101

• Conformations of trimethyl phosphite: a matrix isolation infrared and ab initio study.

  The journal of physical chemistry. A 20110908

• Development of miracle medicines from sialic acids.

  Proceedings of the Japan Academy. Series B, Physical and biological sciences 20110610

• 5-Fluoro-1,3-dihydro-2,1-benzoxaborol-1-ol.

  Acta crystallographica. Section E, Structure reports online 20110201

• Tetra-μ-acetato-κO:O'-bis-{[N-(4-chloro-phen-yl)-4-methyl-pyridin-2-amine-κN]copper(II)}.

  Acta crystallographica. Section E, Structure reports online 20100901

• Tetra-μ-acetato-κO:O'-bis-{[4-methyl-N-(4-methyl-phen-yl)pyridin-2-amine-κN]copper(II)}.

  Acta crystallographica. Section E, Structure reports online 20100901

• 2-(2-Naphth-yl)-1,3-dioxane.

  Acta crystallographica. Section E, Structure reports online 20100201

• Preparation of silane-coated TiO2 nanoparticles in supercritical CO2.

  Journal of colloid and interface science 20091015

• Recent synthetic studies leading to structural revisions of marine natural products.

  Marine drugs 20090901

• Electroosmotic flow-based pump for liquid chromatography on a planar microchip.

  Analytical chemistry 20081101

• Synthesis of (+)-cortistatin A.

  Journal of the American Chemical Society 20080611

• Controlled copper-mediated chlorination of phenol rings under mild conditions.

  Inorganic chemistry 20070611

• Vinylogous Mukaiyama aldol reactions with 4-oxy-2-trimethylsilyloxypyrroles: relevance to castanospermine synthesis.

  Beilstein journal of organic chemistry 20070101

• Novel synthesis of the ortho ester derivative of 4,5-epoxymorphinan.

  Organic letters 20060202

• Microwave-assisted synthesis of imidazoles: reaction of p-toluenesulfonylmethyl isocyanide and polymer-bound imines.

  Bioorganic & medicinal chemistry letters 20050815

• Ni(II) Tol-BINAP-catalyzed enantioselective orthoester alkylations of N-acylthiazolidinethiones.

  Journal of the American Chemical Society 20050803

• Bismuth compounds in organic synthesis. A one-pot synthesis of homoallyl ethers and homoallyl acetates from aldehydes catalyzed by bismuth triflate.

  The Journal of organic chemistry 20050318

• 4-(9-fluorenylmethyloxycarbonyl)phenylhydrazine (FmPH): a new chromophoric reagent for quantitative monitoring of solid-phase aldehydes(1-3).

  The Journal of organic chemistry 20040709

• Preparation of resin-bound N-(alpha-methoxyalkyl)amides: an advantageous use of solid-phase chemistry for the handling of unstable precursors of the versatile N-acyliminium ions.

  Chemistry (Weinheim an der Bergstrasse, Germany) 20010601