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142995-30-0

Boc-3,4-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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  • 142995-30-0 Structure

  • Basic information

    1. Product Name: Boc-3,4-Dimethy-L-Phenylalanine
    2. Synonyms: Boc-3,4-Dimethy-L-Phenylalanine;Boc-Phe(3,4-Me2)-OH;BOC-3,4-DIMETHYL-L-PHENYLALANINE
    3. CAS NO:142995-30-0
    4. Molecular Formula: C16H23NO4
    5. Molecular Weight: 293.35812
    6. EINECS: N/A
    7. Product Categories: N/A
    8. Mol File: 142995-30-0.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-3,4-Dimethy-L-Phenylalanine(CAS DataBase Reference)
    10. NIST Chemistry Reference: Boc-3,4-Dimethy-L-Phenylalanine(142995-30-0)
    11. EPA Substance Registry System: Boc-3,4-Dimethy-L-Phenylalanine(142995-30-0)

  • 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: 142995-30-0(Hazardous Substances Data)

142995-30-0 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 142995-30-0 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,4,2,9,9 and 5 respectively; the second part has 2 digits, 3 and 0 respectively.
Calculate Digit Verification of CAS Registry Number 142995-30:
(8*1)+(7*4)+(6*2)+(5*9)+(4*9)+(3*5)+(2*3)+(1*0)=150
150 % 10 = 0
So 142995-30-0 is a valid CAS Registry Number.

142995-30-0Downstream Products

142995-30-0Relevant 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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