791625-59-7 Usage
Uses
Used in Pharmaceutical Industry:
BOC-D-2,4-DIMETHYLPHE is used as a key intermediate in the synthesis of various pharmaceutical compounds. Its ability to undergo selective reactions due to the BOC protecting group makes it a valuable asset in the development of new drugs and therapeutic agents.
Used in Agrochemical Industry:
In the agrochemical sector, BOC-D-2,4-DIMETHYLPHE serves as a crucial building block for the creation of pesticides and other agricultural chemicals. Its versatility in organic synthesis allows for the production of effective and targeted agrochemicals.
Used in Organic Synthesis:
BOC-D-2,4-DIMETHYLPHE is utilized as a versatile intermediate in organic synthesis for the preparation of a wide range of chemical compounds. The BOC protecting group enables selective reactions, enhancing the compound's synthetic utility.
Used in Peptide Chemistry:
BOC-D-2,4-DIMETHYLPHE is employed as a component in peptide chemistry, where the BOC group's acid-labile nature allows for the stepwise assembly of peptide sequences. This selective deprotection is essential for the synthesis of complex peptide structures.
Overall, BOC-D-2,4-DIMETHYLPHE's applications are diverse, reflecting its importance in the synthesis and production of various chemical entities across different industries.
Check Digit Verification of cas no
The CAS Registry Mumber 791625-59-7 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 7,9,1,6,2 and 5 respectively; the second part has 2 digits, 5 and 9 respectively.
Calculate Digit Verification of CAS Registry Number 791625-59:
(8*7)+(7*9)+(6*1)+(5*6)+(4*2)+(3*5)+(2*5)+(1*9)=197
197 % 10 = 7
So 791625-59-7 is a valid CAS Registry Number.
791625-59-7Relevant 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.
