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Fmoc-L-Glutamic acid 1-tert-butyl ester is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

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    Cas No: 84793-07-7

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  • 84793-07-7 Structure
  • Basic information

    1. Product Name: Fmoc-L-Glutamic acid 1-tert-butyl ester
    2. Synonyms: L-GLUTAMIC ACID, N-[(9H-FLUOREN-9-YLMETHOXY)CARBONYL]-, 1-(1,1-DIMETHYLETHYL) ESTER;N-α-Fmoc-L-glutamic acid α-tert butyl ester;Fmoc glutamic acid butyl ester;(S)-4-((((9H-fluoren-9-yl)Methoxy)carbonyl)aMino)-5-(tert-butoxy)-5-oxopentanoic acid;N-FMoc-L-glutaMic acid 1-tert-butyl ester;Fmoc-L-glutamic acid α-tert-butyl ester≥ 98% (HPLC, Chiral purity);N-FMOC-L-GLUTAMIC ACID-1-T-BUTYL ESTER;N-ALPHA-(9-FLUORENYLMETHOXYCARBONYL)-L-GLUTAMIC ACID ALPHA-T-BUTYL ESTER
    3. CAS NO:84793-07-7
    4. Molecular Formula: C24H27NO6
    5. Molecular Weight: 425.47
    6. EINECS: N/A
    7. Product Categories: Glutamic acid [Glu, E]
    8. Mol File: 84793-07-7.mol
  • Chemical Properties

    1. Melting Point: 78-80 °C
    2. Boiling Point: 638.1 °C at 760 mmHg
    3. Flash Point: 339.7 °C
    4. Appearance: /
    5. Density: 1.232 g/cm3
    6. Refractive Index: N/A
    7. Storage Temp.: Store at RT.
    8. Solubility: N/A
    9. PKA: 4.46±0.10(Predicted)
    10. CAS DataBase Reference: Fmoc-L-Glutamic acid 1-tert-butyl ester(CAS DataBase Reference)
    11. NIST Chemistry Reference: Fmoc-L-Glutamic acid 1-tert-butyl ester(84793-07-7)
    12. EPA Substance Registry System: Fmoc-L-Glutamic acid 1-tert-butyl ester(84793-07-7)
  • 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: 84793-07-7(Hazardous Substances Data)

84793-07-7 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 84793-07-7 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 8,4,7,9 and 3 respectively; the second part has 2 digits, 0 and 7 respectively.
Calculate Digit Verification of CAS Registry Number 84793-07:
(7*8)+(6*4)+(5*7)+(4*9)+(3*3)+(2*0)+(1*7)=167
167 % 10 = 7
So 84793-07-7 is a valid CAS Registry Number.

84793-07-7SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 16, 2017

Revision Date: Aug 16, 2017

1.Identification

1.1 GHS Product identifier

Product name (4S)-4-(9H-fluoren-9-ylmethoxycarbonylamino)-5-[(2-methylpropan-2-yl)oxy]-5-oxopentanoic acid

1.2 Other means of identification

Product number -
Other names Fmoc-L-Glu-O-t-Bu

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:84793-07-7 SDS

84793-07-7Relevant articles and documents

Preparation method of N-fluorenylmethoxycarbonyl-gamma-(S-triphenylmethyl-cysteamine)-L-glutamic acid

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Paragraph 0065, (2020/10/05)

The invention provides a preparation method of N-fluorenylmethoxycarbonyl-gamma-(S-triphenylmethyl-cysteamine)-L-glutamic acid. The preparation method mainly solves the technical problems of complexity, long period, high cost, and low yield of an original process, and comprises the following steps: (1) preparing N-fluorenylmethoxycarbonyl-L-glutamic acid; (2) preparing N-fluorenylmethoxycarbonyl-L-glutamic acid-1-benzyl ester; (3) preparing S-triphenylmethyl cysteamine; (4) preparing N-fluorenylmethoxycarbonyl-gamma-(S-triphenylmethyl-cysteamine)-L-glutamic acid-alpha-benzyl ester; and (5) preparing N-fluorenylmethoxycarbonyl-gamma-(S-triphenylmethyl-cysteamine)-L-glutamic acid. The method is rapid, high in yield and simple in separation and purification, and the used solvent is environment-friendly and is suitable for mass production.

LIGAND-THERAPEUTIC AGENT CONJUGATES, SILICON-BASED LINKERS, AND METHODS FOR MAKING AND USING THEM

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Paragraph 0373; 0374, (2014/09/29)

The present invention relates to ligand-therapeutic agent conjugate compounds, silicon linkers for the conjugate compounds, compositions, methods for making them, and methods for the treatment of cancer using the conjugate compounds. The silicon-based linkers described herein can be used to deliver desired therapeutic agents to particular cells or tissue types targeted by the ligand.

A convenient preparation of several N-linked glycoamino acid building blocks for efficient solid-phase synthesis of glycopeptides

Van Ameijde, Jeroen,Albada, H. Bauke,Liskamp, Rob M.J.

, p. 1042 - 1049 (2007/10/03)

A high yielding route for the preparation of several Boc- and Fmoc-protected N-linked glycopeptide monomers was presented. It was found that these building blocks can be used for the solid-phase synthesis of glycopeptides or glycopeptidomimetics. A number of short glycopeptides- collagen mimics was prepared to demonstrate this applicability. The protocol employed was expected to be suitable for the synthesis of any desired N-linked glycopeptide.

Folate analogues. 33. Synthesis of folate and antifolate poly-γ-glutamates by [(9-fluorenylmethoxy)oxy]carbonyl chemistry and biological evaluation of certain methotrexate polyglutamate polylysine conjugates as inhibitors of the growth of H35 hepatoma cel

Abraham,Nair,Kisliuk,Gaumont,Galivan

, p. 711 - 717 (2007/10/02)

Representative examples of folate and antifolate poly-γ-glutamyl metabolites were synthesized via the [(9-fluorenylmethoxy)oxy]carbonyl (Fmoc) chemistry using the KH polyamide resin. Polyglutamate yields were consistently better in all cases compared to t

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