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Boc-3,4-Dimethy-D-Phenylalanine is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

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  • 1213310-14-5 Structure
  • Basic information

    1. Product Name: Boc-3,4-Dimethy-D-Phenylalanine
    2. Synonyms: Boc-3,4-Dimethy-D-Phenylalanine;Boc-D-Phe(3,4-Me2)-OH;BOC-3,4-DIMETHYL-D-PHENYLALANINE
    3. CAS NO:1213310-14-5
    4. Molecular Formula: C16H23NO4
    5. Molecular Weight: 293.35812
    6. EINECS: N/A
    7. Product Categories: N/A
    8. Mol File: 1213310-14-5.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-D-Phenylalanine(CAS DataBase Reference)
    10. NIST Chemistry Reference: Boc-3,4-Dimethy-D-Phenylalanine(1213310-14-5)
    11. EPA Substance Registry System: Boc-3,4-Dimethy-D-Phenylalanine(1213310-14-5)
  • 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: 1213310-14-5(Hazardous Substances Data)

1213310-14-5 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 1213310-14-5 includes 10 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 7 digits, 1,2,1,3,3,1 and 0 respectively; the second part has 2 digits, 1 and 4 respectively.
Calculate Digit Verification of CAS Registry Number 1213310-14:
(9*1)+(8*2)+(7*1)+(6*3)+(5*3)+(4*1)+(3*0)+(2*1)+(1*4)=75
75 % 10 = 5
So 1213310-14-5 is a valid CAS Registry Number.

1213310-14-5Downstream Products

1213310-14-5Relevant 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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