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CAS

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186023-39-2

L-Serine, N-[(9H-fluoren-9-ylmethoxy)carbonyl]-L-valyl-, phenylmethyl ester is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

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  • 186023-39-2 Structure

  • Basic information

    1. Product Name: L-Serine, N-[(9H-fluoren-9-ylmethoxy)carbonyl]-L-valyl-, phenylmethyl ester
    2. Synonyms:
    3. CAS NO:186023-39-2
    4. Molecular Formula: C30H32N2O6
    5. Molecular Weight: 516.594
    6. EINECS: N/A
    7. Product Categories: N/A
    8. Mol File: 186023-39-2.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: L-Serine, N-[(9H-fluoren-9-ylmethoxy)carbonyl]-L-valyl-, phenylmethyl ester(CAS DataBase Reference)
    10. NIST Chemistry Reference: L-Serine, N-[(9H-fluoren-9-ylmethoxy)carbonyl]-L-valyl-, phenylmethyl ester(186023-39-2)
    11. EPA Substance Registry System: L-Serine, N-[(9H-fluoren-9-ylmethoxy)carbonyl]-L-valyl-, phenylmethyl ester(186023-39-2)

  • 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: 186023-39-2(Hazardous Substances Data)

186023-39-2 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 186023-39-2 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,8,6,0,2 and 3 respectively; the second part has 2 digits, 3 and 9 respectively.
Calculate Digit Verification of CAS Registry Number 186023-39:
(8*1)+(7*8)+(6*6)+(5*0)+(4*2)+(3*3)+(2*3)+(1*9)=132
132 % 10 = 2
So 186023-39-2 is a valid CAS Registry Number.

186023-39-2Relevant articles and documents

Salicylaldehyde ester-induced chemoselective peptide ligations: Enabling generation of natural peptidic linkages at the serine/threonine sites

Li, Xuechen,Lam, Hiu Yung,Zhang, Yinfeng,Chan, Chun Kei

supporting information; experimental part, p. 1724 - 1727 (2010/12/18)

A serine/threonine-based chemoselective ligation method is described. It uses an O-salicylaldehyde ester at the C-terminus, reacting with N-terminal serine or threonine to realize peptide ligations. The utility of the O-salicylaldehyde ester enables the rapid coupling reaction and the production of an N,O-benzylidene acetal intermediate, which is readily converted into natural peptidic linkages (Xaa-Ser/Thr) at the ligation site.

The total synthesis of bistratamides F-I

You, Shu-Li,Kelly, Jeffery W.

, p. 241 - 249 (2007/10/03)

The total synthesis of bistratamides F-I (2-5) have been achieved in overall yields of 3, 10, 13, and 27%, respectively. The thiazole substructure was prepared utilizing a MnO2 oxidation of a thiazoline, synthesized from a Val-Cys dipeptide usi

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