126991-59-1 Usage
Description
8-(4-CHLORO-PHENYL)-1,4-DIOXA-SPIRO[4.5]DECAN-8-OL, with the CAS number 126991-59-1, is a white solid compound that is useful in organic synthesis. It is characterized by its unique spiro-structure and the presence of a chlorophenyl group, which may contribute to its reactivity and potential applications in various chemical processes.
Uses
Used in Organic Synthesis:
8-(4-CHLORO-PHENYL)-1,4-DIOXA-SPIRO[4.5]DECAN-8-OL is used as a synthetic intermediate for the development of various organic compounds. Its unique structure and functional groups make it a valuable building block in the synthesis of pharmaceuticals, agrochemicals, and other specialty chemicals.
Used in Pharmaceutical Industry:
In the pharmaceutical industry, 8-(4-CHLORO-PHENYL)-1,4-DIOXA-SPIRO[4.5]DECAN-8-OL is used as a key intermediate in the synthesis of drug candidates. Its presence in the molecular structure can impart specific biological activities, such as anti-inflammatory, analgesic, or antimicrobial properties, depending on the final compound's design.
Used in Agrochemical Industry:
8-(4-CHLORO-PHENYL)-1,4-DIOXA-SPIRO[4.5]DECAN-8-OL is also utilized in the agrochemical industry as a precursor for the development of new pesticides or herbicides. Its chemical properties may contribute to the effectiveness of these products in controlling pests and weeds, thus supporting agricultural productivity.
Used in Specialty Chemicals:
In the specialty chemicals sector, 8-(4-CHLORO-PHENYL)-1,4-DIOXA-SPIRO[4.5]DECAN-8-OL is employed as a component in the formulation of various products, such as dyes, fragrances, and coatings. Its unique properties can enhance the performance and characteristics of these specialty chemicals, making them suitable for specific applications.
Check Digit Verification of cas no
The CAS Registry Mumber 126991-59-1 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,2,6,9,9 and 1 respectively; the second part has 2 digits, 5 and 9 respectively.
Calculate Digit Verification of CAS Registry Number 126991-59:
(8*1)+(7*2)+(6*6)+(5*9)+(4*9)+(3*1)+(2*5)+(1*9)=161
161 % 10 = 1
So 126991-59-1 is a valid CAS Registry Number.
InChI:InChI=1/C14H17ClO3/c15-12-3-1-11(2-4-12)13(16)5-7-14(8-6-13)17-9-10-18-14/h1-4,16H,5-10H2
126991-59-1Relevant articles and documents
Desymmetrizing Isomerization of Alkene via Thiazolinyl Iminoquinoline Cobalt Catalysis
Liu, Wenbo,Zheng, Yushan,Mao, Yihui,Chen, Jieping,Ren, Xiang,Cheng, Zhaoyang,Lu, Zhan
supporting information, p. 1158 - 1163 (2022/02/14)
We report a cobalt-catalyzed desymmetrizing isomerization of exo-cyclic alkenes to generate chiral 1-methylcyclohexene derivatives with good yields and enantioselectivities. A novel chiral thiazolinyl iminoquinoline ligand and its cobalt complex were desi
Visible Light Mediated Generation of trans-Arylcyclohexenes and Their Utilization in the Synthesis of Cyclic Bridged Ethers
Day, Jon I.,Singh, Kamaljeet,Trinh, Winston,Weaver, Jimmie D.
supporting information, p. 9934 - 9941 (2018/07/25)
While accessible via UV-irradiation of cis-cyclohexene, trans-cyclohexene has thus far been an investigation driven by curiosity, and due primarily to its short lifespan, has until recently not been employed for productive synthesis. Herein, we present st
A Versatile Route to Unstable Diazo Compounds via Oxadiazolines and their Use in Aryl–Alkyl Cross-Coupling Reactions
Greb, Andreas,Poh, Jian-Siang,Greed, Stephanie,Battilocchio, Claudio,Pasau, Patrick,Blakemore, David C.,Ley, Steven V.
, p. 16602 - 16605 (2017/12/13)
Coupling of readily available boronic acids and diazo compounds has emerged recently as a powerful metal-free carbon–carbon bond forming method. However, the difficulty in forming the unstable diazo compound partner in a mild fashion has hitherto limited their general use and the scope of the transformation. Here, we report the application of oxadiazolines as precursors for the generation of an unstable family of diazo compounds using flow UV photolysis and their first use in divergent protodeboronative and oxidative C(sp2)?C(sp3) cross-coupling processes, with excellent functional-group tolerance.
