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327621-02-3

2-(S)-tert-butoxycarbonylamino-3-[4-(2-formylphenoxy)phenyl]propionic acid 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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  • 327621-02-3 Structure

  • Basic information

    1. Product Name: 2-(S)-tert-butoxycarbonylamino-3-[4-(2-formylphenoxy)phenyl]propionic acid methyl ester
    2. Synonyms: 2-(S)-tert-butoxycarbonylamino-3-[4-(2-formylphenoxy)phenyl]propionic acid methyl ester
    3. CAS NO:327621-02-3
    4. Molecular Formula:
    5. Molecular Weight: 399.444
    6. EINECS: N/A
    7. Product Categories: N/A
    8. Mol File: 327621-02-3.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: 2-(S)-tert-butoxycarbonylamino-3-[4-(2-formylphenoxy)phenyl]propionic acid methyl ester(CAS DataBase Reference)
    10. NIST Chemistry Reference: 2-(S)-tert-butoxycarbonylamino-3-[4-(2-formylphenoxy)phenyl]propionic acid methyl ester(327621-02-3)
    11. EPA Substance Registry System: 2-(S)-tert-butoxycarbonylamino-3-[4-(2-formylphenoxy)phenyl]propionic acid methyl ester(327621-02-3)

  • 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: 327621-02-3(Hazardous Substances Data)

327621-02-3 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 327621-02-3 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 3,2,7,6,2 and 1 respectively; the second part has 2 digits, 0 and 2 respectively.
Calculate Digit Verification of CAS Registry Number 327621-02:
(8*3)+(7*2)+(6*7)+(5*6)+(4*2)+(3*1)+(2*0)+(1*2)=123
123 % 10 = 3
So 327621-02-3 is a valid CAS Registry Number.

327621-02-3Relevant articles and documents

Copper-Promoted O-Arylation of the Phenol Side Chain of Tyrosine Using Triarylbismuthines

Gagnon, Alexandre,Hébert, Martin,Le Roch, Adrien

supporting information, p. 5363 - 5367 (2020/08/27)

A general method for the O-arylation of the side chain of tyrosine using triarylbismuth reagents is reported. The reaction is mediated by copper diacetate, operates at 50 °C under oxygen in dichloromethane in the presence of pyridine, shows excellent functional group compatibility, and retains the integrity of the stereogenic center. The protocol was used to arylate the tyrosine residue of dipeptides and tripeptides.

Application of Negishi cross-coupling to the synthesis of the cyclic tripeptides OF4949-III and K-13

Nolasco, Luca,Gonzalez, Manuel Perez,Caggiano, Lorenzo,Jackson, Richard F. W.

experimental part, p. 8280 - 8289 (2010/02/17)

(Chemical Equation Presented) Syntheses of the cyclic tripeptides OF4949-III 1 and K-13 2 are reported, in which the key steps are intermolecular and intramolecular Negishi cross-coupling reactions, respectively. In addition, the synthesis of a protected

Pd-catalysed C-C macrocyclisation of a simple tripeptide: Efficient total synthesis of K-13

Perez-Gonzalez,Jackson

, p. 2423 - 2424 (2007/10/03)

The cyclic tripeptide K-13 has been prepared in 11 steps from commercially available starting materials (11% overall yield); the key step is the Pd-catalysed macrocyclisation of the zinc reagent prepared by selective insertion of zinc into the aliphatic C

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