86912-84-7 Usage
Uses
Used in Organic Synthesis:
1-(3-Chlorophenoxy)-3-butyn-2-ol, 97% is used as a building block for the synthesis of various pharmaceuticals and agrochemicals, contributing to the development of new drugs and chemical products.
Used in Chemical Synthesis:
1-(3-Chlorophenoxy)-3-butyn-2-ol, 97% is used as a reagent in the synthesis of chemical compounds with biological and medicinal applications, enhancing the creation of novel substances for research and industry.
Used in Pharmaceutical Industry:
1-(3-Chlorophenoxy)-3-butyn-2-ol, 97% is used as a key component in the development of new drugs, thanks to its versatility in organic synthesis and its ability to act as a nucleophile in alkylation and acylation reactions.
Used in Agrochemical Industry:
1-(3-Chlorophenoxy)-3-butyn-2-ol, 97% is used as a building block for the preparation of agrochemicals, playing a role in the development of new products for agricultural applications.
Check Digit Verification of cas no
The CAS Registry Mumber 86912-84-7 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 8,6,9,1 and 2 respectively; the second part has 2 digits, 8 and 4 respectively.
Calculate Digit Verification of CAS Registry Number 86912-84:
(7*8)+(6*6)+(5*9)+(4*1)+(3*2)+(2*8)+(1*4)=167
167 % 10 = 7
So 86912-84-7 is a valid CAS Registry Number.
InChI:InChI=1/C10H9ClO2/c1-2-9(12)7-13-10-5-3-4-8(11)6-10/h1,3-6,9,12H,7H2
86912-84-7Relevant academic research and scientific papers
An Enantioconvergent Synthesis of (R)-4-Aryloxy-1-butyne-3-ols for Prostanoid Side Chains
Fox, Martin E.,Jackson, Mark,Lennon, Ian C.,McCague, Raymond,Parratt, Julian S.
, p. 50 - 56 (2007/10/03)
The single enantiomer title alcohols, useful as co-side chain precursors for pharmaceutically important prostaglandin analogues were synthesised from the corresponding racemic alcohols by a convenient 4-step sequence. After enzymatic acylation of the alco
Process for the preparation of prostaglandin precursors
-
, (2008/06/13)
A propargylic alcohol, enriched in the (R)-enantiomer, has the formula wherein R is C1-4 alkoxy, halogen, or C1-4 alkyl optionally substituted by OH or halogen. This is prepared by the steps of: (a) enantioselective (R)-esterification of the racemic alcohol using any acyl donor and a first enzyme; (b) removal of the untreated (S)-alcohol; and (c) enantioselective hydrolysis of the (R)-ester, using a second enzyme.
