24347-54-4 Usage
Description
(S)-4-methylpentane-1,2-diol, with the molecular formula C6H14O2, is a chiral diol that exists in two distinct enantiomers. This chemical compound is recognized for its significance in the production of pharmaceuticals, fine chemicals, polyester resins, polyurethanes, and plasticizers. Its ability to enhance the flexibility and durability of polymers makes it a vital component in a wide range of industrial applications, contributing to the development of numerous consumer products and industrial goods.
Uses
Used in Pharmaceutical and Fine Chemicals Industry:
(S)-4-methylpentane-1,2-diol is used as a building block for the synthesis of various pharmaceuticals and fine chemicals. Its chiral nature allows for the creation of specific enantiomers that can exhibit different biological activities, making it a valuable component in drug development.
Used in Polymer and Plastics Industry:
(S)-4-methylpentane-1,2-diol is used as a key component in the manufacturing of polyester resins, polyurethanes, and plasticizers. It serves to increase the flexibility and durability of these polymers, which is crucial for their performance in various applications, such as coatings, adhesives, and elastomers.
Used in Industrial Applications:
(S)-4-methylpentane-1,2-diol is utilized in a wide range of industrial applications due to its ability to improve the properties of polymers. It plays a crucial role in the development of numerous consumer products and industrial goods, contributing to their enhanced performance and durability.
Check Digit Verification of cas no
The CAS Registry Mumber 24347-54-4 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 2,4,3,4 and 7 respectively; the second part has 2 digits, 5 and 4 respectively.
Calculate Digit Verification of CAS Registry Number 24347-54:
(7*2)+(6*4)+(5*3)+(4*4)+(3*7)+(2*5)+(1*4)=104
104 % 10 = 4
So 24347-54-4 is a valid CAS Registry Number.
InChI:InChI=1/C6H14O2/c1-5(2)3-6(8)4-7/h5-8H,3-4H2,1-2H3
24347-54-4Relevant articles and documents
Fast synthesis of complex enantiopure heterocyclic scaffolds by a tandem sequence of simple transformations on α-hydroxyaldehydes
Cannillo, Alexandre,Norsikian, Stephanie,Retailleau, Pascal,Dau, Marie-Elise Tran Huu,Iorga, Bogdan I.,Beau, Jean-Marie
supporting information, p. 9127 - 9131 (2013/07/26)
Two tandems are faster than one! Properly sequenced reactions initiated by the Petasis aminoalcohol synthesis from boronic acids, diallylamine, and α-hydroxyaldehydes, including free aldoses, leads to rapid construction of complex enantiopure structures (see scheme). Copyright
Synthesis of new chiral ionic liquids from α-hydroxycarboxylic acids
Poterala, Marcin,Plenkiewicz, Jan
, p. 294 - 299 (2011/05/17)
New functionalized optically active N-methylimidazolium ionic liquids with an asymmetric center at the β-position to the imdazole ring were synthesized as bromide salts from optically active α-hydroxycarboxylic acids. The bromide anions were exchanged by carboxylate anions with Amberlite IRA 400 ionic exchange resin.
N-(α-chloroalkyloxycarbonyl)pyrrolidines as a source of oxygenated d1- reagents
Ortiz, Javier,Guijarro, Albert,Yus, Miguel
, p. 3005 - 3012 (2007/10/03)
Reaction of the N-(α-chloroalkyloxycarbonyl)pyrrolidines 1 with lithium powder and a catalytic amount of 4,4'-di-tertbutylbiphenyl (DTBB, 2.5 mol-%) in the presence of different electrophiles [iBuCHO, tBuCHO, PhCHO, Et2CO, (CH2)5CO, PhCOMe, Ph2CO, MeaSiCl], in THF at temperatures ranging between -78 and -60°C leads after hydrolysis with water, to the expected functionalized carbamates 2. Deprotection of compounds 2, derived from carbonyl compounds, with lithium hydroxide in a mixture of ethanol and water at 80°C affords the corresponding 1,2-diols 3.
