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261165-17-7

Boc-2,5-Dimethy-L-Phenylalanine is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

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  • 261165-17-7 Structure

  • Basic information

    1. Product Name: Boc-2,5-Dimethy-L-Phenylalanine
    2. Synonyms: Boc-2,5-Dimethy-L-Phenylalanine;Boc-Phe(2,5-Me2)-OH;BOC-2,5-DIMETHYL-L-PHENYLALANINE
    3. CAS NO:261165-17-7
    4. Molecular Formula: C16H23NO4
    5. Molecular Weight: 293.35812
    6. EINECS: N/A
    7. Product Categories: N/A
    8. Mol File: 261165-17-7.mol

  • Chemical Properties

    1. Melting Point: N/A
    2. Boiling Point: N/A
    3. Flash Point: N/A
    4. Appearance: /
    5. Density: N/A
    6. Refractive Index: N/A
    7. Storage Temp.: N/A
    8. Solubility: N/A
    9. CAS DataBase Reference: Boc-2,5-Dimethy-L-Phenylalanine(CAS DataBase Reference)
    10. NIST Chemistry Reference: Boc-2,5-Dimethy-L-Phenylalanine(261165-17-7)
    11. EPA Substance Registry System: Boc-2,5-Dimethy-L-Phenylalanine(261165-17-7)

  • Safety Data

    1. Hazard Codes: N/A
    2. Statements: N/A
    3. Safety Statements: N/A
    4. WGK Germany:
    5. RTECS:
    6. HazardClass: N/A
    7. PackingGroup: N/A
    8. Hazardous Substances Data: 261165-17-7(Hazardous Substances Data)

261165-17-7 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 261165-17-7 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 2,6,1,1,6 and 5 respectively; the second part has 2 digits, 1 and 7 respectively.
Calculate Digit Verification of CAS Registry Number 261165-17:
(8*2)+(7*6)+(6*1)+(5*1)+(4*6)+(3*5)+(2*1)+(1*7)=117
117 % 10 = 7
So 261165-17-7 is a valid CAS Registry Number.

261165-17-7Downstream Products

261165-17-7Relevant articles and documents

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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