85418-23-1 Usage
Description
(S)-4-Benzyloxy-1,3-butanediol, also known as (S)-Ethyleneglycol monobenzyl ether, is a chiral molecule that consists of a benzyl group attached to a diol. It is a colorless liquid with a mild, sweet odor and is relatively stable under normal conditions. (S)-4-Benzyloxy-1,3-butanediol is commonly used as a building block in organic synthesis and serves as a starting material for the production of pharmaceuticals, agrochemicals, and other specialty chemicals.
Uses
Used in Organic Synthesis:
(S)-4-Benzyloxy-1,3-butanediol is used as a building block in organic synthesis for the creation of various chemical compounds. Its unique structure allows for versatile reactions and the formation of a wide range of products.
Used in Pharmaceutical Production:
(S)-4-Benzyloxy-1,3-butanediol is used as a starting material in the production of pharmaceuticals. Its properties make it suitable for the development of new drugs and active pharmaceutical ingredients.
Used in Agrochemical Production:
(S)-4-Benzyloxy-1,3-butanediol is also utilized as a starting material in the production of agrochemicals, contributing to the development of pesticides and other agricultural chemicals.
Used as a Solvent:
(S)-4-Benzyloxy-1,3-butanediol is used as a solvent in various chemical reactions due to its ability to dissolve a wide range of substances.
Used as an Intermediate in Chemical Reactions:
It serves as an intermediate in chemical reactions, facilitating the synthesis of complex molecules and compounds.
Used in the Production of Polymers and Resins:
(S)-4-Benzyloxy-1,3-butanediol has potential applications in the production of polymers and resins, which are used in a variety of industries for coatings, adhesives, and plastics.
Used in Pharmaceutical Formulations:
Due to its solubility and pharmacokinetic properties, (S)-4-Benzyloxy-1,3-butanediol may be used in pharmaceutical formulations to improve the delivery and effectiveness of drugs.
Check Digit Verification of cas no
The CAS Registry Mumber 85418-23-1 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 8,5,4,1 and 8 respectively; the second part has 2 digits, 2 and 3 respectively.
Calculate Digit Verification of CAS Registry Number 85418-23:
(7*8)+(6*5)+(5*4)+(4*1)+(3*8)+(2*2)+(1*3)=141
141 % 10 = 1
So 85418-23-1 is a valid CAS Registry Number.
InChI:InChI=1/C11H16O3/c12-7-6-11(13)9-14-8-10-4-2-1-3-5-10/h1-5,11-13H,6-9H2/t11-/m0/s1
85418-23-1Relevant articles and documents
Enantioselective total synthesis of (+)-reserpine
Rajapaksa, Naomi S.,McGowan, Meredeth A.,Rienzo, Matthew,Jacobsen, Eric N.
, p. 706 - 709 (2013/04/10)
A catalytic, enantioselective synthesis of (+)-reserpine is reported. The route features a highly diastereoselective, chiral catalyst-controlled formal aza-Diels-Alder reaction between a 6-methoxytryptamine-derived dihydro-β-carboline and an enantioenriched α-substituted enone to form a key tetracyclic intermediate. This approach addresses the challenge of setting the C3 stereogenic center by using catalyst control. Elaboration of the tetracycle to (+)-reserpine includes an intramolecular aldol cyclization and a highly diastereoselective hydrogenation of a sterically hindered enoate.
Synthesis of chiral 1,3-diols by radical-mediated regioselective opening of 2,3-epoxy alcohols using cp2TiCl
Chakraborty, Tushar K,Das, Sanjib
, p. 2313 - 2315 (2007/10/03)
Radical-mediated opening of chiral 2,3-epoxy alcohols 1a-e, regioselectively at the 2-position, using cp2TiCl in the absence of a hydrogen source leads to the formation of the 1,3-diols 2a-e.
The asymmetric dihydroxylation of some alkenyl 2-acetylamino-2-deoxy-β-d-glucopyranosides: The preparation of optically pure epoxides as putative inhibitors of chitinases
Fairweather, Jon K.,Stick, Robert V.,Tilbrook, D. Matthew G.
, p. 471 - 482 (2007/10/03)
Various alkenyl 2-acetylamino-2-deoxy-β-D-glucopyranosides have been subjected to the Sharpless asymmetric dihydroxylation protocol to yield the corresponding diols, albeit with somewhat disappointing stereoselectivity. An alternative, more traditional ap
