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(R)-2-methyloxetane is a chiral cyclic ether compound belonging to the class of oxetane compounds. It has a molecular formula of C5H10O, a molecular weight of 86.13 g/mol, and exists as a colorless liquid with a boiling point of 48-50°C. Being insoluble in water but soluble in organic solvents, (R)-2-methyloxetane serves as a versatile building block in organic synthesis.

81244-76-0

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81244-76-0 Usage

Uses

Used in Pharmaceutical and Agrochemical Industries:
(R)-2-methyloxetane is utilized as a key building block in the synthesis of various pharmaceuticals and agrochemicals. Its unique structure and reactivity make it a valuable component in the development of new and improved drugs and agricultural products.
Used as a Solvent:
In the chemical industry, (R)-2-methyloxetane serves as a solvent for a range of applications. Its solubility in organic solvents and its ability to dissolve a variety of compounds make it a useful medium for chemical processes.
Used as a Reagent in Chemical Reactions:
(R)-2-methyloxetane is also employed as a reagent in various chemical reactions. Its properties allow it to participate in a number of organic synthesis processes, contributing to the formation of desired products in the field of medicinal chemistry and chemical synthesis.

Check Digit Verification of cas no

The CAS Registry Mumber 81244-76-0 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 8,1,2,4 and 4 respectively; the second part has 2 digits, 7 and 6 respectively.
Calculate Digit Verification of CAS Registry Number 81244-76:
(7*8)+(6*1)+(5*2)+(4*4)+(3*4)+(2*7)+(1*6)=120
120 % 10 = 0
So 81244-76-0 is a valid CAS Registry Number.

81244-76-0SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 18, 2017

Revision Date: Aug 18, 2017

1.Identification

1.1 GHS Product identifier

Product name (R)-(-)-2-Methyloxetane

1.2 Other means of identification

Product number -
Other names 2-METHYLOXETANE

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:81244-76-0 SDS

81244-76-0Downstream Products

81244-76-0Relevant academic research and scientific papers

Access to (S)-2-Methyloxetane and the Precursor (S)-1,3-Butanediol of Hight Enantiomeric Purity

Hintzer, Klaus,Koppenhoefer, Bernhard,Schurig, Volker

, p. 3850 - 3854 (2007/10/02)

(S)-2-Methyloxetane (1) and its precursor (S)-1,3-butanediol (2) were prepared in low to moderate chemical yield with less than 0.5percent racemization from (S)-ethyl lactate (4) and from (2S,3S)-allothreonine (14b).For the first time the enantiomeric purities of both the starting material and the product (1) were carefully determined by high-precision capillary gas chromatography on optically active resolving stationary phases.The validity of the quadrant rule, correlating the relative configuration of alkyloxiranes with the order of elution from manganese(II) bis (3) by complexation gas chromatography, is also confirmed for 2-methyloxetane (1).

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