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7093-67-6

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  • 2-[[2-[[2-[[2-[(2-aminoacetyl)amino]acetyl]amino]acetyl]amino]acetyl]amino]acetic acid

    Cas No: 7093-67-6

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7093-67-6 Usage

Chemical Properties

White powder

Uses

Pentaglycine could be a useful tumor necrosis factor receptor 2 agonist.

Definition

ChEBI: A pentapeptide comprised of five glycine residues.

Check Digit Verification of cas no

The CAS Registry Mumber 7093-67-6 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 7,0,9 and 3 respectively; the second part has 2 digits, 6 and 7 respectively.
Calculate Digit Verification of CAS Registry Number 7093-67:
(6*7)+(5*0)+(4*9)+(3*3)+(2*6)+(1*7)=106
106 % 10 = 6
So 7093-67-6 is a valid CAS Registry Number.
InChI:InChI=1/C10H17N5O6/c11-1-6(16)12-2-7(17)13-3-8(18)14-4-9(19)15-5-10(20)21/h1-5,11H2,(H,12,16)(H,13,17)(H,14,18)(H,15,19)(H,20,21)

7093-67-6 Well-known Company Product Price

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  • Sigma

  • (G5755)  Gly-Gly-Gly-Gly-Gly  

  • 7093-67-6

  • G5755-25MG

  • 460.98CNY

  • Detail
  • Sigma

  • (G5755)  Gly-Gly-Gly-Gly-Gly  

  • 7093-67-6

  • G5755-1G

  • 4,698.72CNY

  • Detail

7093-67-6SDS

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 pentaglycine

1.2 Other means of identification

Product number -
Other names Gly-Gly-Gly-Gly-Gly-OH

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:7093-67-6 SDS

7093-67-6Relevant articles and documents

Mechanochemical Prebiotic Peptide Bond Formation**

Cindro, Nikola,Grube?i?, Sa?a,Hernández, José G.,Me?trovi?, Ernest,Stolar, Tomislav,U?arevi?, Krunoslav

supporting information, p. 12727 - 12731 (2021/05/07)

The presence of amino acids on the prebiotic Earth, either stemming from endogenous chemical routes or delivered by meteorites, is consensually accepted. Prebiotically plausible pathways to peptides from inactivated amino acids are still unclear as most oligomerization approaches rely on thermodynamically disfavored reactions in solution. Now, a combination of prebiotically plausible minerals and mechanochemical activation enables the oligomerization of glycine at ambient temperature in the absence of water. Raising the reaction temperature increases the degree of oligomerization concomitantly with the formation of a commonly unwanted cyclic glycine dimer (DKP). However, DKP is a productive intermediate in the mechanochemical oligomerization of glycine. The findings of this research show that mechanochemical peptide bond formation is a dynamic process that provides alternative routes towards oligopeptides and establishes new synthetic approaches for prebiotic chemistry.

PEPTIDE FORMATION FROM AMINO ACID WITH PARTICULATE SEMICONDUCTOR PHOTOCATALYSTS

Onoe, Jun,Kawai, Tomoji,Kawai, Shichio

, p. 1667 - 1670 (2007/10/02)

Peptides of diglycine to pentaglycine are formed from glycine under irradiation in the presence of particulate semiconductor photocatalysts such as TiO2, CdS, CdSe, MoS2, In2O3, and GaP, with and without Pt deposition.Platinization of the semiconductors efficiently enhanced the yield of the peptides.

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