328956-56-5 Usage
Uses
Used in Pharmaceutical Synthesis:
1-(2-BOC-AMINO-PHENYL)-ETHANOL is used as a key intermediate for the development of pharmaceuticals due to its ability to be incorporated into complex molecular structures. Its BOC-protected amino group ensures that the molecule can be selectively deprotected and functionalized, facilitating the synthesis of a wide range of therapeutic agents.
Used in Agrochemical Production:
In the agrochemical industry, 1-(2-BOC-AMINO-PHENYL)-ETHANOL is utilized as a versatile building block for the creation of various agrochemicals. Its chemical properties allow for the synthesis of compounds that can be used in pest control, crop protection, and other agricultural applications.
Used in Specialty Chemicals:
1-(2-BOC-AMINO-PHENYL)-ETHANOL is employed as a precursor in the synthesis of specialty chemicals, which are often used in niche applications such as high-performance materials, dyes, and other industrial chemicals. Its unique structure and functional groups make it suitable for the development of these specialized compounds.
Used in Organic Chemistry Research:
As a valuable tool in organic chemistry, 1-(2-BOC-AMINO-PHENYL)-ETHANOL is used in research settings to explore new synthetic pathways, develop novel reactions, and understand the reactivity of protected amino groups. Its ease of functionalization and deprotection makes it an ideal candidate for studying various organic transformations.
Check Digit Verification of cas no
The CAS Registry Mumber 328956-56-5 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 3,2,8,9,5 and 6 respectively; the second part has 2 digits, 5 and 6 respectively.
Calculate Digit Verification of CAS Registry Number 328956-56:
(8*3)+(7*2)+(6*8)+(5*9)+(4*5)+(3*6)+(2*5)+(1*6)=185
185 % 10 = 5
So 328956-56-5 is a valid CAS Registry Number.
InChI:InChI=1/C13H19NO3/c1-9(15)10-7-5-6-8-11(10)14-12(16)17-13(2,3)4/h5-9,15H,1-4H3,(H,14,16)
328956-56-5Relevant academic research and scientific papers
N-Heterocyclic Carbene-Catalyzed Synthesis of 2-Aryl Indoles
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Paragraph 0065, (2015/11/27)
Transition metal-free catalytic methods for access to 2-arylindole compounds.
N-heterocyclic-carbene-catalyzed synthesis of 2-aryl indoles
Hovey, M. Todd,Check, Christopher T.,Sipher, Alexandra F.,Scheidt, Karl A.
supporting information, p. 9603 - 9607 (2014/10/15)
A convergent and efficient transition-metal-free catalytic synthesis of 2-aryl-indoles has been developed. The interception of a highly reactive and transient aza-ortho-quinone methide by an acyl anion equivalent generated through N-hetereocyclic carbene catalysis is central to this successful strategy. High yields and a wide scope as well as the streamlined synthesis of a kinase inhibitor are reported. Umpolung: N-heterocyclic carbene catalysis is used for the convergent and efficient transition-metal-free synthesis of 2-aryl-indoles. The interception of a highly reactive and transient aza-ortho-quinone methide by an acyl anion equivalent is central to this successful strategy. The reaction exhibits high yields and a wide scope, and it has been applied to a streamlined synthesis of a kinase inhibitor.
Enzymatic kinetic resolution of tert-butyl 2-(1-Hydroxyethyl) phenylcarbamate, a key intermediate to chiral organoselenanes and organotelluranes
Piovan, Leandro,Pasquini, Monica D.,Andrade, Leandro H.
experimental part, p. 8098 - 8109 (2011/11/06)
The enzymatic kinetic resolution of tert-butyl 2-(1-hydroxyethyl) phenylcarbamate via lipase-catalyzed transesterification reaction was studied. We investigated several reaction conditions and the carbamate was resolved by Candida antarctica lipase B (CAL
