60456-23-7 Usage
Description
(S)-Oxiranemethanol, also known as Glycerol, is a colorless to light yellow liquid with highly reactive epoxy and hydroxyl groups. It is a versatile organic compound that serves as a monomer in the preparation of various polymers and is also used in the synthesis of chiral (E)-allylic alcohol side-chains for prostacyclin and prostaglandin frameworks.
Uses
Used in Polymer Industry:
(S)-Oxiranemethanol is used as a monomer for the production of various polymers such as polyesters, polycarbonates, polyurethanes, and polyamides. Its high reactivity allows for the formation of versatile polymer structures with a wide range of applications.
Used in Pharmaceutical Industry:
(S)-Oxiranemethanol is used as a key intermediate in the synthesis of chiral (E)-allylic alcohol side-chains, which are essential for the development of prostacyclin and prostaglandin frameworks. These frameworks have significant implications in the treatment of various medical conditions.
Used in Detergent Industry:
(S)-Oxiranemethanol is used as a raw material in the preparation of detergents, contributing to their cleaning and emulsifying properties.
Used in Rubber Industry:
(S)-Oxiranemethanol is employed as a component in the production of rubber, enhancing its properties and performance.
Used in Perfume Industry:
(S)-Oxiranemethanol is used as a base material in the creation of various perfumes, contributing to their unique scents and long-lasting qualities.
Used in Fabric Dye Industry:
(S)-Oxiranemethanol is utilized in the production of fabric dyes, improving their colorfastness and performance on different types of fabrics.
Used in Cosmetics Industry:
(S)-Oxiranemethanol is used as an ingredient in the formulation of cosmetics, providing moisturizing and emollient properties to the products.
Used in Paint and Varnish Industry:
(S)-Oxiranemethanol is employed in the production of paints and varnishes, enhancing their adhesion, durability, and overall performance.
Check Digit Verification of cas no
The CAS Registry Mumber 60456-23-7 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 6,0,4,5 and 6 respectively; the second part has 2 digits, 2 and 3 respectively.
Calculate Digit Verification of CAS Registry Number 60456-23:
(7*6)+(6*0)+(5*4)+(4*5)+(3*6)+(2*2)+(1*3)=107
107 % 10 = 7
So 60456-23-7 is a valid CAS Registry Number.
InChI:InChI=1/C3H6O2/c4-1-3-2-5-3/h3-4H,1-2H2
60456-23-7Relevant articles and documents
INTERMEDIATE USEFUL FOR SYNTHESIZING QUINOLYLPYRROLOPYRIMIDYL FUSED-RING COMPOUND
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Paragraph 0290; 0292-0294, (2018/03/31)
PROBLEM TO BE SOLVED: To provide a method for synthesizing or producing efficiently a quinolylpyrrolopyrimidyl fused-ring compound which has an epidermal growth factor receptor (EGFR)-inhibiting activity. SOLUTION: This invention relates to a compound expressed by formula (1), or its salt. (R1 is H, nitro, amino, hydroxy, ether, alkylthio, arylthio, etc.; R2 is halogen, a hydroxyl group, quinolyl, etc.; R3 is H or a protective group of an amino group; R4 is aldehyde or a carboxyl group when n=0, or is halogen or a hydroxyl group when n=1; R5 is an amino group or a protective group when a bond part is a single bond, or is oxo, imino, or =NRb when the bond part is a double bond; and Rb is aralkyl, acyl, alkyl sulfonyl, etc.). SELECTED DRAWING: None COPYRIGHT: (C)2018,JPOandINPIT
Total Syntheses of Perenniporides
Morita, Masao,Ohmori, Ken,Suzuki, Keisuke
supporting information, p. 5634 - 5637 (2015/12/01)
The total syntheses of perenniporide A (1) and related compounds have been achieved. Starting from 1,3,5-trifluorobenzene (9), difluorodienone 6 was obtained by oxidative dearomatization, which served as a platform for the high-pressure cycloaddition and for the introduction of the C3-methoxy group. The synthesis allowed access to the natural congeners 2 and 3, enabling assignment of the absolute structures of these natural products.
Engineering Homochiral Metal-Organic Frameworks by Spatially Separating 1D Chiral Metal-Peptide Ladders: Tuning the Pore Size for Enantioselective Adsorption
Stylianou, Kyriakos C.,G?mez, Laura,Imaz, Inhar,Verdugo-Escamilla, Crist?bal,Ribas, Xavi,Maspoch, Daniel
supporting information, p. 9964 - 9969 (2015/07/07)
The reaction of the chiral dipeptide glycyl-L(S)-glutamate with CoII ions produces chiral ladders that can be used as rigid 1D building units. Spatial separation of these building units with linkers of different lengths allows the engineering of homochiral porous MOFs with enhanced pore sizes, pore volumes, and surface areas. This strategy enables the synthesis of a family of isoreticular MOFs, in which the pore size dictates the enantioselective adsorption of chiral molecules (in terms of their size and enantiomeric excess).