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Boc-2,3-Dimethyl-L-Phenylalanine is a chemical compound with the molecular formula C15H23NO4. It is a derivative of the amino acid phenylalanine, with two methyl groups attached to the 2 and 3 positions of the phenyl ring and a tert-butoxycarbonyl (Boc) protecting group attached to the amino group. Boc-2,3-Dimethy-L-Phenylalanine is an important tool for organic chemists and is widely available for purchase from chemical suppliers.

849440-32-0

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849440-32-0 Usage

Uses

Used in Pharmaceutical Industry:
Boc-2,3-Dimethyl-L-Phenylalanine is used as a building block in peptide synthesis for the production of pharmaceuticals and biologically active peptides. Its unique structure allows for the creation of complex organic molecules with potential therapeutic applications.
Used in Organic Chemistry Research:
Boc-2,3-Dimethyl-L-Phenylalanine is used as a chiral building block in the synthesis of complex organic molecules. Its presence in various chemical reactions can lead to the development of new compounds with specific properties and functions, contributing to the advancement of organic chemistry.

Check Digit Verification of cas no

The CAS Registry Mumber 849440-32-0 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 8,4,9,4,4 and 0 respectively; the second part has 2 digits, 3 and 2 respectively.
Calculate Digit Verification of CAS Registry Number 849440-32:
(8*8)+(7*4)+(6*9)+(5*4)+(4*4)+(3*0)+(2*3)+(1*2)=190
190 % 10 = 0
So 849440-32-0 is a valid CAS Registry Number.

849440-32-0Downstream Products

849440-32-0Relevant academic research and scientific papers

Asymmetric synthesis of all six regioisomers of N-boc-dimethylphenylalanines

Ouchi, Hidekazu,Kumagai, Midori,Sakurada, Shinobu,Takahata, Hiroki

, p. 505 - 514 (2007/10/03)

All possible regioisomers of dimethyl-substituted (S)-phenylalanine were efficiently synthesized by reacting the Ni(II)-complex of the chiral Schiff base of glycine with (S)-2-N-(N-benzylprolyl)-aminobenzophenone.

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