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41167-51-5

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41167-51-5 Usage

Description

[(4R,5S)-2,2,5-trimethyl-1,3-dioxolan-4-yl]methanol is a derivative of dioxolane, characterized by its five-membered heterocyclic structure and a hydroxyl group. This colorless liquid with a mild, sweet odor is known for its unique chemical properties and reactivity, making it a versatile compound with potential applications in organic synthesis, pharmaceutical research, and as a solvent and reagent in various chemical reactions.

Uses

Used in Organic Synthesis:
[(4R,5S)-2,2,5-trimethyl-1,3-dioxolan-4-yl]methanol is used as a building block for the synthesis of complex organic molecules, leveraging its unique reactivity and structural features to facilitate the creation of novel compounds.
Used in Pharmaceutical Research:
In the pharmaceutical industry, [(4R,5S)-2,2,5-trimethyl-1,3-dioxolan-4-yl]methanol serves as a key intermediate in the development of new drugs, thanks to its potential to be modified and incorporated into a wide range of medicinal compounds.
Used as a Solvent:
[(4R,5S)-2,2,5-trimethyl-1,3-dioxolan-4-yl]methanol is utilized as a solvent in various chemical reactions, providing a suitable medium for the reactants to mix and interact, thus facilitating the desired chemical transformations.
Used as a Reagent:
[(4R,5S)-2,2,5-trimethyl-1,3-dioxolan-4-yl]methanol also functions as a reagent, participating directly in chemical reactions to produce the desired products, taking advantage of its specific chemical properties.
It is crucial to handle [(4R,5S)-2,2,5-trimethyl-1,3-dioxolan-4-yl]methanol with care due to its potential health hazards if not properly managed.

Check Digit Verification of cas no

The CAS Registry Mumber 41167-51-5 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 4,1,1,6 and 7 respectively; the second part has 2 digits, 5 and 1 respectively.
Calculate Digit Verification of CAS Registry Number 41167-51:
(7*4)+(6*1)+(5*1)+(4*6)+(3*7)+(2*5)+(1*1)=95
95 % 10 = 5
So 41167-51-5 is a valid CAS Registry Number.

41167-51-5SDS

SAFETY DATA SHEETS

According to Globally Harmonized System of Classification and Labelling of Chemicals (GHS) - Sixth revised edition

Version: 1.0

Creation Date: Aug 12, 2017

Revision Date: Aug 12, 2017

1.Identification

1.1 GHS Product identifier

Product name [(4R,5S)-2,2,5-trimethyl-1,3-dioxolan-4-yl]methanol

1.2 Other means of identification

Product number -
Other names 4-deoxy-2,3-O-isopropylidene-L-threytol

1.3 Recommended use of the chemical and restrictions on use

Identified uses For industry use only.
Uses advised against no data available

1.4 Supplier's details

1.5 Emergency phone number

Emergency phone number -
Service hours Monday to Friday, 9am-5pm (Standard time zone: UTC/GMT +8 hours).

More Details:41167-51-5 SDS

41167-51-5Relevant articles and documents

Enantioselective sensing of insect pheromones in water

Chen, Junyi,Gill, Adam D.,Hickey, Briana L.,Hooley, Richard J.,Millar, Jocelyn G.,Zhong, Wenwan,Zou, Yunfan

supporting information, p. 13341 - 13344 (2021/12/17)

An arrayed combination of water-soluble deep cavitands and cationic dyes has been shown to optically sense insect pheromones at micromolar concentration in water. Machine learning approaches were used to optimize the most effective array components, which

Versicolactones A and B: Total synthesis and structure revision

Wang, Liping,Zhu, Weiming

supporting information, p. 6729 - 6731 (2013/11/19)

To further determine absolute configurations of versicolactones A and B, total synthesis of versicolactones A and B and their six stereoisomers were reported in this Letter. The 1H and 13C NMR spectra of the synthetic erythro-stereoisomers matched perfectly with those of the natural products. Combined with the comparison of the specific rotations, the absolute configuration of versicolactones A and B were revised as (4Z,6R,7S)- and (4E,6R,7S)- from the corresponding (4Z,6R,7R)- and (4E,6R,7R)-6,7-dihydroxyocta- 2,4-dien-4-lactone, respectively.

Synthesis and bioluminescence-inducing properties of autoinducer (S)-4,5-dihydroxypentane-2,3-dione and its enantiomer

Kadirvel, Manikandan,Stimpson, William T.,Moumene-Afifi, Souad,Arsic, Biljana,Glynn, Nicola,Halliday, Nigel,Williams, Paul,Gilbert, Peter,McBain, Andrew J.,Freeman, Sally,Gardiner, John M.

scheme or table, p. 2625 - 2628 (2010/07/13)

The autoinducer (4S)-4,5-dihydroxypentane-2,3-dione ((S)-DPD, AI-2) facilitates chemical communication, termed 'quorum sensing', amongst a wide range of bacteria, The synthesis of (S)-DPD is challenging in part due to its instability. Herein we report a novel synthesis of (S)-DPD via (2S)-2,3-O-isopropylidene glyceraldehyde, through Wittig, dihydroxylation and oxidation reactions, with a complimentary asymmetric synthesis to a key precursor. Its enantiomer (R)-DPD, was prepared from d-mannitol via (2R)-2,3-O-isopropylideneglyceraldehyde. The synthesized enantiomers of DPD have AI-2 bioluminescence-inducing properties in the Vibrio harveyi BB170 strain.

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