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3-N-BOC-3-(2-FLUOROPHENYL)PROPIONIC ACID is a chemical compound widely recognized in the field of organic chemistry for its significant role in pharmaceutical applications. The "BOC" in its name signifies a protective group that is integral to peptide synthesis, a process critical in the creation of peptide-based drugs. 3-N-BOC-3-(2-FLUOROPHENYL)PROPIONIC ACID also features a fluorophenyl group, which is a phenyl ring (a functional group composed of six carbon atoms in a cyclic structure) that has been fluorinated to modify the molecule's chemical characteristics. The propionic acid component of the compound imparts its acidic properties. This chemical is a key player in drug design and development, being extensively utilized in the synthesis of effective pharmaceuticals.

284493-56-7

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284493-56-7 Usage

Uses

Used in Pharmaceutical Industry:
3-N-BOC-3-(2-FLUOROPHENYL)PROPIONIC ACID is used as a key intermediate in the synthesis of peptide-based drugs for its ability to protect the peptide during the synthesis process. The BOC group ensures that the peptide remains stable and unreacted until the desired point in the synthesis, at which it can be selectively removed to yield the final drug product.
Used in Drug Design and Development:
3-N-BOC-3-(2-FLUOROPHENYL)PROPIONIC ACID is used as a building block in the design of novel pharmaceuticals, leveraging its fluorophenyl and propionic acid components to create molecules with specific chemical behaviors. The fluorination of the phenyl ring can influence the compound's reactivity, solubility, and interaction with biological targets, making it a valuable tool in the development of new therapeutic agents.
Used in Organic Chemistry Research:
3-N-BOC-3-(2-FLUOROPHENYL)PROPIONIC ACID is used as a model compound in organic chemistry research to study the effects of fluorination on the properties of aromatic rings. This can provide insights into the design of new molecules with tailored chemical and biological properties, contributing to the advancement of the field.

Check Digit Verification of cas no

The CAS Registry Mumber 284493-56-7 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 2,8,4,4,9 and 3 respectively; the second part has 2 digits, 5 and 6 respectively.
Calculate Digit Verification of CAS Registry Number 284493-56:
(8*2)+(7*8)+(6*4)+(5*4)+(4*9)+(3*3)+(2*5)+(1*6)=177
177 % 10 = 7
So 284493-56-7 is a valid CAS Registry Number.
InChI:InChI=1/C14H18FNO4/c1-14(2,3)20-13(19)16-11(8-12(17)18)9-6-4-5-7-10(9)15/h4-7,11H,8H2,1-3H3,(H,16,19)(H,17,18)

284493-56-7 Well-known Company Product Price

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  • Alfa Aesar

  • (L19804)  3-(Boc-amino)-3-(2-fluorophenyl)propionic acid, 98+%   

  • 284493-56-7

  • 250mg

  • 347.0CNY

  • Detail
  • Alfa Aesar

  • (L19804)  3-(Boc-amino)-3-(2-fluorophenyl)propionic acid, 98+%   

  • 284493-56-7

  • 1g

  • 1076.0CNY

  • Detail

284493-56-7SDS

SAFETY DATA SHEETS

According to Globally Harmonized System of Classification and Labelling of Chemicals (GHS) - Sixth revised edition

Version: 1.0

Creation Date: Aug 19, 2017

Revision Date: Aug 19, 2017

1.Identification

1.1 GHS Product identifier

Product name 3-(2-fluorophenyl)-3-[(2-methylpropan-2-yl)oxycarbonylamino]propanoic acid

1.2 Other means of identification

Product number -
Other names -

1.3 Recommended use of the chemical and restrictions on use

Identified uses For industry use only.
Uses advised against no data available

1.4 Supplier's details

1.5 Emergency phone number

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Service hours Monday to Friday, 9am-5pm (Standard time zone: UTC/GMT +8 hours).

More Details:284493-56-7 SDS

284493-56-7Upstream product

284493-56-7Downstream Products

284493-56-7Relevant academic research and scientific papers

BICYCLIC-PYRIMIDINEDIONE COMPOUNDS

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Paragraph 0249; 0250, (2016/07/27)

The present invention provides novel bicyclic pyrimidinedione compounds that are useful for the treatment of hypertrophic cardiomyopathy (HCM) and conditions associated with left ventricular hypertrophy or diastolic dysfunction. The synthesis and characterization of the compounds is described, as well as methods for treating HCM and other forms of heart disease.

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