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FMOC-D-ASP(OBZL)-OH is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

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  • 150009-58-8 Structure
  • Basic information

    1. Product Name: FMOC-D-ASP(OBZL)-OH
    2. Synonyms: FMOC-D-ASPARTIC ACID BETA-BENZYL ESTER;FMOC-D-ASPARTIC ACID(OBZL)-OH;FMOC-D-ASP(OBZL)-OH;N-ALPHA-(9-FLUORENYLMETHOXYCARBONYL)-D-ASPARTIC ACID BETA-BENZYL ESTER;N-[(9H-Fluoren-9-ylmethoxy)carbonyl]-D-aspartic acid 4-(phenylmethyl) ester;Fmoc-D-aspartic acid β-benzyl ester≥ 99% (HPLC);N-Fmoc-D-aspartic acid 4-benzyl ester;(9H-Fluoren-9-yl)MethOxy]Carbonyl D-Asp(OBzl)-OH
    3. CAS NO:150009-58-8
    4. Molecular Formula: C26H23NO6
    5. Molecular Weight: 445.46
    6. EINECS: N/A
    7. Product Categories: N/A
    8. Mol File: 150009-58-8.mol
  • Chemical Properties

    1. Melting Point: N/A
    2. Boiling Point: 687.2±55.0 °C(Predicted)
    3. Flash Point: N/A
    4. Appearance: /Solid
    5. Density: 1.310±0.06 g/cm3(Predicted)
    6. Refractive Index: N/A
    7. Storage Temp.: Store at RT.
    8. Solubility: N/A
    9. PKA: 3.54±0.23(Predicted)
    10. CAS DataBase Reference: FMOC-D-ASP(OBZL)-OH(CAS DataBase Reference)
    11. NIST Chemistry Reference: FMOC-D-ASP(OBZL)-OH(150009-58-8)
    12. EPA Substance Registry System: FMOC-D-ASP(OBZL)-OH(150009-58-8)
  • 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: 150009-58-8(Hazardous Substances Data)

150009-58-8 Usage

Uses

Fmoc-d-asp(obzl)-oh is a useful intermediate for organic synthesis.

Check Digit Verification of cas no

The CAS Registry Mumber 150009-58-8 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,5,0,0,0 and 9 respectively; the second part has 2 digits, 5 and 8 respectively.
Calculate Digit Verification of CAS Registry Number 150009-58:
(8*1)+(7*5)+(6*0)+(5*0)+(4*0)+(3*9)+(2*5)+(1*8)=88
88 % 10 = 8
So 150009-58-8 is a valid CAS Registry Number.

150009-58-8 Well-known Company Product Price

  • Brand
  • (Code)Product description
  • CAS number
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  • Alfa Aesar

  • (H66422)  N-Fmoc-D-aspartic acid 4-benzyl ester, 95%   

  • 150009-58-8

  • 250mg

  • 294.0CNY

  • Detail
  • Alfa Aesar

  • (H66422)  N-Fmoc-D-aspartic acid 4-benzyl ester, 95%   

  • 150009-58-8

  • 1g

  • 784.0CNY

  • Detail
  • Alfa Aesar

  • (H66422)  N-Fmoc-D-aspartic acid 4-benzyl ester, 95%   

  • 150009-58-8

  • 5g

  • 2940.0CNY

  • Detail

150009-58-8SDS

SAFETY DATA SHEETS

According to Globally Harmonized System of Classification and Labelling of Chemicals (GHS) - Sixth revised edition

Version: 1.0

Creation Date: Aug 18, 2017

Revision Date: Aug 18, 2017

1.Identification

1.1 GHS Product identifier

Product name FMOC-D-ASP(OBZL)-OH

1.2 Other means of identification

Product number -
Other names Fmoc-Ala-Cl

1.3 Recommended use of the chemical and restrictions on use

Identified uses For industry use only.
Uses advised against no data available

1.4 Supplier's details

1.5 Emergency phone number

Emergency phone number -
Service hours Monday to Friday, 9am-5pm (Standard time zone: UTC/GMT +8 hours).

More Details:150009-58-8 SDS

150009-58-8Relevant articles and documents

Rapid access to Asp/Glu sidechain hydrazides as thioester precursors for peptide cyclization and glycosylation

Barnes, Natalie G.,Nyandoro, Kudakwashe,Jin, Hanzhang,Macmillan, Derek

, p. 1006 - 1009 (2021)

Head-to-sidechain macrocylic peptides, and neoglycopeptides, were readily prepared by site-specific amidation of aspartic and glutamic acid sidechain hydrazides. Hydrazides, serving as latent thioesters, were introduced through regioselective opening of the corresponding Nα-Fmoc protected anhydride precursors.

Activity of (+)-Discadenine as a Plant Cytokinin

Mik, Václav,Mi?ková, Zuzana,Dole?al, Karel,Frébort, Ivo,Pospí?il, Tomá?

, p. 2136 - 2140 (2017)

Discadenine (1), a self-spore germination inhibitor from the cellular slim mold Dictyostelium discoideum, is structurally related to the plant hormone cytokinin. This compound was synthesized from l-aspartic acid, and its activities were confirmed by three classical cytokinin bioassays as well as by using binding and activation assays with the Arabidopsis cytokinin receptors AHK3 and CRE1/AHK4.

Oligomeric aminodiol-containing compounds, libraries thereof, and process of preparing the same

-

, (2008/06/13)

Oligomeric compounds comprising a plurality of aminodiol monomer subunits joined by linking groups are provided, as well as libraries of such compounds and processes for preparing the oligomeric compounds and libraries.

Combinatorial libraries having aminodiol monomer subunits

-

, (2008/06/13)

Combinatorial libraries are constructed to include aminodiol monomer subunits connected by phosphodiester, phosphorothioate, or phosphoramidate linking moieties. Combinatorial libraries of the invention feature a plurality of functional groups attached to

Ready protease-catalyzed synthesis of carbohydrate-amino acid conjugates.

Boyer,Stanchev,Fairbanks,Davis

, p. 1908 - 1909 (2007/10/03)

The protease-catalyzed synthesis of amino acid est-carbohydrate conjugates as glycopeptide analogues has been achieved in a highly regioselective and carbohydrate-specific manner using amino acid vinyl ester acyl donors and minimally or completely unprotected carbohydrate acyl acceptors, which together probed active sites of proteases to reveal yield efficiencies that are modulated by the carbohydrate C-2 substitutent, and that may be exploited to allow selective one-pot syntheses.

Phosphoramidate and phosphorothiomidate oligomeric compounds

-

, (2008/06/13)

Compounds are provided having structure (I), wherein the L groups are backbone segments, the Y and T groups are functional groups for interacting with target molecules of interest, the X groups are oxygen or sulfur and the E groups are H, conjugate groups or intermediate groups used during the synthesis of the compounds and wherein the compounds are prepared using H phosphonate type chemistry wherein the functional groups are added during an oxidation step or during a coupling step. STR1

Guanidinyl and related cell adhesion modulation compounds

-

, (2008/06/13)

Guanidinyl-containing compounds, and related compounds and salts, useful as cell receptor antagonists for modulating cell adhesion via integrin receptors and/or fibronectin receptors, are disclosed. Methods for synthesizing, testing, formulating, and usin

Aspartic acid derivatives

-

, (2008/06/13)

New compounds N-α-9-fluorenylmethoxycarbonyl-aspartic acid-β-1-adamantyl esters are stable under the basic condition of the normal peptide condensation process and do not form succinimide. Peptides containing aspartic acid can be synthesized with high purity and at high yields by using N-α-9-fluorenylmethoxycarbonyl-aspartic acid-β-1-adamantyl ester.

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