2163-42-0 | 2-Methyl-1,3-propanediol

Packsize	Purity	Availability	Price	Discounted Price
5g	98%	in stock	$16.00	$11.00
100g	98%	in stock	$16.00	$12.00
500g	98%	in stock	$59.00	$41.00

Description

• Catalog Number: AB62558
• Chemical Name: 2-Methyl-1,3-propanediol
• CAS Number: 2163-42-0
• Molecular Formula: C4H10O2
• Molecular Weight: 90.121
• MDL Number: MFCD00082586
• SMILES: OCC(CO)C

Computed Properties

• Complexity: 24.7
• Covalently-Bonded Unit Count: 1
• Heavy Atom Count: 6
• Hydrogen Bond Acceptor Count: 2
• Hydrogen Bond Donor Count: 2
• Rotatable Bond Count: 2
• XLogP3: -0.3

Literature

• The transcription factor AmrZ utilizes multiple DNA binding modes to recognize activator and repressor sequences of Pseudomonas aeruginosa virulence genes.

  PLoS pathogens 20120401

• Direct generation of acyclic polypropionate stereopolyads via double diastereo- and enantioselective iridium-catalyzed crotylation of 1,3-diols: beyond stepwise carbonyl addition in polyketide construction.

  Journal of the American Chemical Society 20110817

• Optimization of culture conditions to produce high yields of active Acetobacter sp. CCTCC M209061 cells for anti-Prelog reduction of prochiral ketones.

  BMC biotechnology 20110101

• Inducing single-molecule magnetism in a family of loop-of-loops aggregates: heterometallic Mn(40)Na(4) clusters and the homometallic Mn(44) analogue.

  Journal of the American Chemical Society 20101117

• A Mn₁₅ single-molecule magnet consisting of a supertetrahedron incorporated in a loop.

  Dalton transactions (Cambridge, England : 2003) 20100528

• The difficult case of crystallization and structure solution for the ParC55 breakage-reunion domain of topoisomerase IV from Streptococcus pneumoniae.

  PloS one 20080101

• Regulated-stereoselective construction of thirteen stereogenic centers necessary for the frame of (+)-discodermolide, based on iterative Lewis acid-promoted aldol reactions.

  The Journal of organic chemistry 20031017

• A multiphasic hollow fiber reactor for the whole-cell bioconversion of 2-methyl-1,3-propanediol to (r)-beta-hydroxyisobutyric acid.

  Biotechnology progress 20010101