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110683-03-9

N-(all-trans-retinoyl)-L-phenylalanine methyl ester is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

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  • 110683-03-9 Structure

  • Basic information

    1. Product Name: N-(all-trans-retinoyl)-L-phenylalanine methyl ester
    2. Synonyms: N-(all-trans-retinoyl)-L-phenylalanine methyl ester
    3. CAS NO:110683-03-9
    4. Molecular Formula:
    5. Molecular Weight: 461.645
    6. EINECS: N/A
    7. Product Categories: N/A
    8. Mol File: 110683-03-9.mol

  • Chemical Properties

    1. Melting Point: N/A
    2. Boiling Point: N/A
    3. Flash Point: N/A
    4. Appearance: N/A
    5. Density: N/A
    6. Refractive Index: N/A
    7. Storage Temp.: N/A
    8. Solubility: N/A
    9. CAS DataBase Reference: N-(all-trans-retinoyl)-L-phenylalanine methyl ester(CAS DataBase Reference)
    10. NIST Chemistry Reference: N-(all-trans-retinoyl)-L-phenylalanine methyl ester(110683-03-9)
    11. EPA Substance Registry System: N-(all-trans-retinoyl)-L-phenylalanine methyl ester(110683-03-9)

  • 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: 110683-03-9(Hazardous Substances Data)

110683-03-9 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 110683-03-9 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,1,0,6,8 and 3 respectively; the second part has 2 digits, 0 and 3 respectively.
Calculate Digit Verification of CAS Registry Number 110683-03:
(8*1)+(7*1)+(6*0)+(5*6)+(4*8)+(3*3)+(2*0)+(1*3)=89
89 % 10 = 9
So 110683-03-9 is a valid CAS Registry Number.

110683-03-9Relevant articles and documents

A simple, general and efficient method for O and N-retinoylation. Application to the synthesis of 2-retinoyl-lecithin

Sangmam, Charles,Winum, Jean-Yves,Lucas, Marc,Montero, Jean-Louis,Chavis, Claude

, p. 2945 - 2958 (2007/10/03)

The synthesis of the new 1-stearoyl-2-retinoyl-glycero-3- phosphorylcholine by coupling of retinoic acid and lysolecithin with DCC- DMAP (1.2 eq.) is reported. This method is applied to O and N-retinoylation of uncharged organic substrates such as aliphatic alcohols, free hydroxyl anomeric sugars, aromatic amines and C-protected α-aminoacids.

N-(retinoyl)amino acids, synthesis and chemopreventive activity in vitro

Shealy,Frye,Schiff

, p. 190 - 196 (2007/10/02)

N-(all-trans-Retinoyl)amino acids were synthesized via all-trans-retinoyl chloride and an ester of the amino acid. The retinoyl derivatives of leucine, phenylalanine, alanine, tyrosine, and glutamic acid were prepared. The 13-cis-retinoyl derivatives of l

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