29022-11-5

  • Product Name:Fmoc-Glycine
  • Molecular Formula:C17H15NO4
  • Purity:99%
  • Molecular Weight:297.31
InquiryAdd to cart

Product Details;

CAS#: 29022-11-5

Molecular Formula: C17H15NO4

Appearance: white to light yellow crystal powder

Reputable Factory Supply Hot Sale 29022-11-5 with the Best Price

  • Molecular Formula:C17H15NO4
  • Molecular Weight:297.31
  • Appearance/Colour:white to light yellow crystal powder 
  • Vapor Pressure:9.69E-13mmHg at 25°C 
  • Melting Point:174-178 °C 
  • Refractive Index:1.4500 (estimate) 
  • Boiling Point:545.7 °C at 760 mmHg 
  • PKA:3.89±0.10(Predicted) 
  • Flash Point:283.8 °C 
  • PSA:75.63000 
  • Density:1.316 g/cm3 
  • LogP:3.00060 

Fmoc-Glycine(Cas 29022-11-5) Usage

General Description

The product number for this product was previously 04-12-1001.To obtain a certificate of analysis (CoA) of a lot that begins with the letter “A”, please select the option in the right hand menu “Request a COA for Lot#s starting with A”.

InChI:InChI=1/C17H15NO4/c19-16(20)9-18-17(21)22-10-15-13-7-3-1-5-11(13)12-6-2-4-8-14(12)15/h1-8,15H,9-10H2,(H,18,21)(H,19,20)/p-1

29022-11-5 Relevant articles

Large molecular assembly of amphotericin B formed in ergosterol-containing membrane evidenced by solid-state NMR of intramolecular bridged derivative

Matsumori, Nobuaki,Sawada, Yuri,Murata, Michio

, p. 11977 - 11984 (2006)

Amphotericin B (AmB 1) is known to assem...

Fmoc-Amox, A Suitable Reagent for the Introduction of Fmoc

Kumar, Ashish,Sharma, Anamika,Haimov, Elvira,El-Faham, Ayman,De La Torre, Beatriz G.,Albericio, Fernando

, p. 1533 - 1541 (2017)

Synthesis of most peptides is achieved u...

Synthesis and characterization of a photocleavable collagen-like peptide

Li, Chunqiang,Ornelas, Alfredo,Williams, Kaitlyn N.,Hatch, Kevin A.,Paez, Aurelio,Aguilar, Angela C.,Ellis, Cameron C.,Tasnim, Nishat,Ray, Supriyo,Dirk, Carl W.,Boland, Thomas,Joddar, Binata,Michael, Katja

, p. 1000 - 1013 (2018)

A 34-amino acid long collagen-like pepti...

Oxime carbonates: Novel reagents for the introduction of fmoc and alloc protecting groups, free of side reactions

Khattab, Sherine N.,Subiros-Funosas, Ramon,El-Faham, Ayman,Albericio, Fernando

, p. 3275 - 3280 (2010)

Fmoc and Alloc protecting groups represe...

Fungal Dioxygenase AsqJ Is Promiscuous and Bimodal: Substrate-Directed Formation of Quinolones versus Quinazolinones

Einsiedler, Manuel,Jamieson, Cooper S.,Maskeri, Mark A.,Houk, Kendall N.,Gulder, Tobias A. M.

supporting information, p. 8297 - 8302 (2021/03/01)

Previous studies showed that the FeII/α-...

Dihydroartemisinin and steroid conjugates, and preparation method and application thereof

-

Paragraph 0098-0102, (2019/11/20)

The present invention discloses conjugat...

A 4-OTBS benzyl-based protective group for carboxylic acids

Fang, Zhijun,Li, Yuyao,Xie, Hexin

supporting information, p. 1658 - 1662 (2019/05/29)

Reported herein is a novel 4-OTBS benzyl...

Unwanted hydrolysis or α/β-peptide bond formation: How long should the rate-limiting coupling step take?

Goldschmidt G?z, Viktória,Nagy, Adrienn,Farkas, Viktor,Keszei, Ern?,Perczel, András

, p. 30720 - 30728 (2019/10/28)

Nowadays, in Solid Phase Peptide Synthes...

29022-11-5 Process route

(fluorenylmethoxy)carbonyl chloride
28920-43-6

(fluorenylmethoxy)carbonyl chloride

glycine
56-40-6,18875-39-3,25718-94-9

glycine

N-(fluoren-9-ylmethoxycarbonyl)glycine
29022-11-5

N-(fluoren-9-ylmethoxycarbonyl)glycine

Conditions
Conditions Yield
In ethanol; water; at 60 ℃; for 4h; chemoselective reaction;
85%
(fluorenylmethoxy)carbonyl chloride; glycine; With sodium carbonate; In 1,4-dioxane; water; at 0 - 20 ℃; for 4h;
With hydrogenchloride; In water; pH=2;
85%
With sodium carbonate; N-ethyl-N,N-diisopropylamine; In water; N,N-dimethyl-formamide; 1.) 0 deg C, 30 min; 2.) up to RT, 1 h;
62%
With sodium carbonate;
 
With sodium carbonate; In 1,4-dioxane; water; for 18h; Ambient temperature;
 
With N-ethyl-N,N-diisopropylamine;
 
In acetonitrile; at 20 ℃; for 0.25h; pH=9.2; aq. borate buffer;
 
With sodium carbonate; In 1,4-dioxane; water; at 20 ℃; for 2h;
 
With sodium carbonate; In water; acetone; at 20 ℃; for 2.5h; Cooling with ice;
 
With potassium carbonate; In 1,4-dioxane; water; at 20 ℃; for 12h;
 
4-((tert-butyldimethylsilyl)oxy)benzyl (((9H-fluoren-9-yl)methoxy)carbonyl)glycinate

4-((tert-butyldimethylsilyl)oxy)benzyl (((9H-fluoren-9-yl)methoxy)carbonyl)glycinate

N-(fluoren-9-ylmethoxycarbonyl)glycine
29022-11-5

N-(fluoren-9-ylmethoxycarbonyl)glycine

Conditions
Conditions Yield
With trifluoroacetic acid; In dichloromethane; at 20 ℃; for 0.0833333h; Reagent/catalyst;
97%

29022-11-5 Upstream products

  • 28920-43-6
    28920-43-6

    (fluorenylmethoxy)carbonyl chloride

  • 56-40-6
    56-40-6

    glycine

  • 100803-86-9
    100803-86-9

    3-(9-Fluorenylmethoxycarbonyl)-benzothiazoline-2-thione

  • 88744-04-1
    88744-04-1

    (9-fluorenyl)methyl pentafluorophenyl carbonate

29022-11-5 Downstream products

  • 61570-87-4
    61570-87-4

    (9H-Fluoren-9-ylmethoxycarbonylamino)-acetic acid trityl ester

  • 113484-74-5
    113484-74-5

    2,5-dioxopyrrolidin-1-yl N-[(9H-fluoren-9-ylmethoxy)carbonyl]glycinate

  • 71989-22-5
    71989-22-5

    Fmoc-Gly-ONp

  • 113534-28-4
    113534-28-4

    Fmoc-Gly-OTDO

Relevant Products

Shopping Cart

Clear Inquiry

CONTACT

Contacts:Haiying

Tel:028 8868 0086

Email:xuehaiying@zybiochem.com

Weekday:9:00~18:00
Contact us