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201334-88-5

BOC-DL-TYR(2,6-DICHLORO-BZL)-OH is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

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  • 201334-88-5 Structure

  • Basic information

    1. Product Name: BOC-DL-TYR(2,6-DICHLORO-BZL)-OH
    2. Synonyms: BOC-O-2,6-DICHLOROBENZYL-DL-TYROSINE;BOC-DL-TYR(2,6-DICHLORO-BZL)-OH;BOC-DL-TYR(2,6-DI-CL-BZL)-OH;BOC-DL-TYROSINE(2,6-DICHLORO-BZL)-OH;BOC-DL-TYR(CL 2-BZL)-OH;N-ALPHA-T-BUTOXYCARBONYL-O-(2,6-DICHLOROBENZYL)-DL-TYROSINE;Boc-O-2,6-dichlorobenzyl-DL-tyrosine≥ 99% (TLC)
    3. CAS NO:201334-88-5
    4. Molecular Formula: C21H23Cl2NO5
    5. Molecular Weight: 440.32
    6. EINECS: N/A
    7. Product Categories: N/A
    8. Mol File: 201334-88-5.mol

  • Chemical Properties

    1. Melting Point: N/A
    2. Boiling Point: 594.0±50.0 °C(Predicted)
    3. Flash Point: N/A
    4. Appearance: /
    5. Density: 1.305±0.06 g/cm3(Predicted)
    6. Refractive Index: N/A
    7. Storage Temp.: Store at RT.
    8. Solubility: N/A
    9. PKA: 2.98±0.10(Predicted)
    10. CAS DataBase Reference: BOC-DL-TYR(2,6-DICHLORO-BZL)-OH(CAS DataBase Reference)
    11. NIST Chemistry Reference: BOC-DL-TYR(2,6-DICHLORO-BZL)-OH(201334-88-5)
    12. EPA Substance Registry System: BOC-DL-TYR(2,6-DICHLORO-BZL)-OH(201334-88-5)

  • 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: 201334-88-5(Hazardous Substances Data)

201334-88-5 Usage

Chemical Properties

White powder

Check Digit Verification of cas no

The CAS Registry Mumber 201334-88-5 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 2,0,1,3,3 and 4 respectively; the second part has 2 digits, 8 and 8 respectively.
Calculate Digit Verification of CAS Registry Number 201334-88:
(8*2)+(7*0)+(6*1)+(5*3)+(4*3)+(3*4)+(2*8)+(1*8)=85
85 % 10 = 5
So 201334-88-5 is a valid CAS Registry Number.

201334-88-5Relevant articles and documents

Synthesis and biological activity of N-substituted aminocarbonyl-1,3- dioxolanes as VLA-4 antagonists

Rehman, Abdul,Soni, Ajay,Naik, Keshav,Nair, Sreeji,Palle, Venkata P.,Dastidar, Sunanda,Ray, Abhijit,Alam,Salman, Mohammad,Cliffe, Ian A.,Sattigeri, Viswajanani

scheme or table, p. 5514 - 5520 (2011/01/12)

A novel set of compounds with a 1,3-dioxolane ring which acts as a proline bioisostere have been successfully designed as VLA-4 receptor antagonists. Compounds (18e), (28j), and (35g) were shown to have high receptor affinities.

A simple method for the alkaline hydrolysis of esters

Theodorou, Vassiliki,Skobridis, Konstantinos,Tzakos, Andreas G.,Ragoussis, Valentine

, p. 8230 - 8233 (2008/03/14)

A very mild and rapid procedure for the efficient alkaline hydrolysis of esters in non-aqueous conditions has been developed, by the use of dichloromethane/methanol (9:1) as solvent. This method conveniently provides both carboxylic acids and alcohols from the corresponding esters and sodium hydroxide in a few minutes at room temperature. A plausible reaction mechanism is proposed.

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