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1-Boc-3-fluoroazetidine-3-carboxylic acid is a chemical compound with the formula C10H17FNO4. It is a Boc-protected amino acid derivative that features a fluorine atom. 1-Boc-3-fluoroazetidine-3... is utilized in the synthesis of peptides and other bioactive molecules due to its unique structure and properties, making it a valuable building block in organic synthesis and pharmaceutical research.

1126650-66-5

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1126650-66-5 Usage

Uses

Used in Pharmaceutical Research:
1-Boc-3-fluoroazetidine-3-carboxylic acid is used as a key intermediate in the synthesis of fluorinated peptides and bioactive molecules. Its incorporation into these molecules can potentially enhance their biological activity and pharmacological properties, such as improved metabolic stability and binding affinity to target receptors.
Used in Organic Synthesis:
In the field of organic synthesis, 1-Boc-3-fluoroazetidine-3-carboxylic acid serves as a versatile building block for the creation of complex organic molecules. Its unique structure allows for various synthetic transformations, enabling the development of novel compounds with potential applications in various industries.
Used in Peptide Synthesis:
1-Boc-3-fluoroazetidine-3-carboxylic acid is used as a Boc-protected amino acid derivative in peptide synthesis. The Boc protection group is crucial for protecting the carboxylic acid group during the synthesis process, allowing for selective activation and coupling of the amino acid to other peptide fragments. This results in the formation of fluorinated peptides with potential therapeutic applications.
Overall, 1-Boc-3-fluoroazetidine-3-carboxylic acid is a valuable compound in various applications across the pharmaceutical and chemical industries, offering unique opportunities for the development of innovative drugs and synthetic compounds.

Check Digit Verification of cas no

The CAS Registry Mumber 1126650-66-5 includes 10 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 7 digits, 1,1,2,6,6,5 and 0 respectively; the second part has 2 digits, 6 and 6 respectively.
Calculate Digit Verification of CAS Registry Number 1126650-66:
(9*1)+(8*1)+(7*2)+(6*6)+(5*6)+(4*5)+(3*0)+(2*6)+(1*6)=135
135 % 10 = 5
So 1126650-66-5 is a valid CAS Registry Number.

1126650-66-5SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 16, 2017

Revision Date: Aug 16, 2017

1.Identification

1.1 GHS Product identifier

Product name tert-butyl 3-fluoro-3-(hydroxymethyl)azetidine-1-carboxylate

1.2 Other means of identification

Product number -
Other names 1-BOC-3-FLUOROAZETIDINE-3-METHANOL

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

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

More Details:1126650-66-5 SDS

1126650-66-5Relevant academic research and scientific papers

N-(Substituted sulfonyl)benzamide derivative and preparation method and pharmaceutical application thereof

-

Paragraph 0593; 0595; 0600-0603, (2019/04/17)

The invention relates to an N-(substituted sulfonyl)benzamide derivative and preparation method and pharmaceutical application thereof, in particular to an N-(substituted sulfonyl)benzamide derivativeshown as general formula (I), preparation method thereof, medicinal salts of the derivative, and their application as therapeutics, especially as Nav1.7 inhibitors, wherein substituents in the general formula (I) shown in the description are defined the same as in the description.

Synthesis of l-Boc-3-fluoroazetidine-3-carboxylic acid

Van Hende, Eva,Verniest, Guido,Deroose, Frederik,Thuring, Jan-Willem,Macdonald, Gregor,De Kimpe, Norbert

experimental part, p. 2250 - 2253 (2009/08/07)

Synthetic strategies toward 3-fluoroazetidine-3-carboxylic acid, a new cyclic fluorinated β-amino acid with high potential as building block in medicinal chemistry, were evaluated. The successful pathway includes the bromoflu-orination of N-(diphenylmethy

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