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Boc-(S)-3-Amino-3-(4-chlorophenyl)propionic acid, also known as Boc-S-4-Cl-L-Phenylalanine, is a chemical compound derived from the amino acid phenylalanine. It features a Boc (tert-butyloxycarbonyl) protecting group that temporarily masks the amino group, facilitating selective reactions in organic synthesis. The 4-chlorophenyl group attached to the molecule is crucial for its biological activity and potential applications in medicine.

479064-90-9

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479064-90-9 Usage

Uses

Used in Pharmaceutical Synthesis:
Boc-(S)-3-Amino-3-(4-chlorophenyl)propionic acid is used as a key intermediate in the synthesis of pharmaceuticals and biologically active compounds. Its unique structure and functional groups make it a valuable building block for creating new drugs and therapeutic agents.
Used in Medicinal Chemistry Research:
In the field of medicinal chemistry, Boc-(S)-3-Amino-3-(4-chlorophenyl)propionic acid serves as a versatile compound for exploring its potential as a lead molecule in drug discovery. Its chemical properties and structural features can be further modified and optimized to enhance its biological activity and therapeutic potential.
Used in Drug Development:
Boc-(S)-3-Amino-3-(4-chlorophenyl)propionic acid has potential applications in the development of new drugs and therapeutic agents. Its unique structure and functional groups can be leveraged to design and synthesize novel compounds with improved pharmacological properties, such as increased potency, selectivity, and reduced side effects.
Used in Chemical Synthesis:
As a chemical compound with a Boc protecting group, Boc-(S)-3-Amino-3-(4-chlorophenyl)propionic acid is used in various chemical synthesis processes. The Boc group allows for selective reactions to occur, protecting the amino group from unwanted side reactions, and enabling the synthesis of more complex and functionalized molecules.

Check Digit Verification of cas no

The CAS Registry Mumber 479064-90-9 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 4,7,9,0,6 and 4 respectively; the second part has 2 digits, 9 and 0 respectively.
Calculate Digit Verification of CAS Registry Number 479064-90:
(8*4)+(7*7)+(6*9)+(5*0)+(4*6)+(3*4)+(2*9)+(1*0)=189
189 % 10 = 9
So 479064-90-9 is a valid CAS Registry Number.
InChI:InChI=1/C14H18ClNO4/c1-14(2,3)20-13(19)16-11(8-12(17)18)9-4-6-10(15)7-5-9/h4-7,11H,8H2,1-3H3,(H,16,19)(H,17,18)/t11-/m0/s1

479064-90-9 Well-known Company Product Price

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  • Aldrich

  • (19343)  (S)-Boc-4-chloro-β-Phe-OH  ≥98.0% (HPLC)

  • 479064-90-9

  • 19343-500MG-F

  • 3,635.19CNY

  • Detail

479064-90-9SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 13, 2017

Revision Date: Aug 13, 2017

1.Identification

1.1 GHS Product identifier

Product name (3S)-3-(4-chlorophenyl)-3-[(2-methylpropan-2-yl)oxycarbonylamino]propanoic acid

1.2 Other means of identification

Product number -
Other names (S)-3-(tert-butoxycarbonylamino)-3-(4-chlorophenyl)propanoic acid

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:479064-90-9 SDS

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