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FMOC-(R)-3-AMINO-4-(2-CHLORO-PHENYL)-BUTYRIC ACID is a chemical compound characterized by its molecular formula C23H22ClNO4. It is a derivative of the amino acid butyric acid, featuring a fluorine-protecting group (FMOC) and a chlorine-substituted phenyl group. FMOC-(R)-3-AMINO-4-(2-CHLORO-PHENYL)-BUTYRIC ACID is known for its unique structure and properties, which make it valuable in various scientific and industrial applications.

268734-29-8

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268734-29-8 Usage

Uses

Used in Chemical Research and Synthesis:
FMOC-(R)-3-AMINO-4-(2-CHLORO-PHENYL)-BUTYRIC ACID is utilized as a key component in the synthesis of peptides and other organic molecules, playing a crucial role in chemical research. Its unique structure allows for the development of novel compounds with potential applications in various fields.
Used in Pharmaceutical Industry:
In the pharmaceutical industry, FMOC-(R)-3-AMINO-4-(2-CHLORO-PHENYL)-BUTYRIC ACID is used as a building block for the development of new drugs. Its potential biological activity and unique chemical properties make it a promising candidate for the creation of innovative therapeutic agents.
Used in Biotechnology:
FMOC-(R)-3-AMINO-4-(2-CHLORO-PHENYL)-BUTYRIC ACID finds application in biotechnology, where it can be employed in the design and synthesis of bioactive peptides and other biomolecules. Its unique structure and properties contribute to the advancement of biotechnological processes and products.
Used in Materials Science:
In materials science, FMOC-(R)-3-AMINO-4-(2-CHLORO-PHENYL)-BUTYRIC ACID is used as a component in the development of new materials with specific properties. Its unique chemical structure allows for the creation of materials with potential applications in various industries, such as electronics, coatings, and adhesives.
Overall, FMOC-(R)-3-AMINO-4-(2-CHLORO-PHENYL)-BUTYRIC ACID is a versatile chemical compound with a wide range of applications across different industries, including chemical research, pharmaceuticals, biotechnology, and materials science. Its unique structure and properties make it a valuable asset in the development of new products and technologies.

Check Digit Verification of cas no

The CAS Registry Mumber 268734-29-8 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 2,6,8,7,3 and 4 respectively; the second part has 2 digits, 2 and 9 respectively.
Calculate Digit Verification of CAS Registry Number 268734-29:
(8*2)+(7*6)+(6*8)+(5*7)+(4*3)+(3*4)+(2*2)+(1*9)=178
178 % 10 = 8
So 268734-29-8 is a valid CAS Registry Number.
InChI:InChI=1/C25H22ClNO4/c26-23-12-6-1-7-16(23)13-17(14-24(28)29)27-25(30)31-15-22-20-10-4-2-8-18(20)19-9-3-5-11-21(19)22/h1-12,17,22H,13-15H2,(H,27,30)(H,28,29)/t17-/m1/s1

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