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3-(N-Boc)pentanedioic acid is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

85185-24-6

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85185-24-6 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 85185-24-6 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 8,5,1,8 and 5 respectively; the second part has 2 digits, 2 and 4 respectively.
Calculate Digit Verification of CAS Registry Number 85185-24:
(7*8)+(6*5)+(5*1)+(4*8)+(3*5)+(2*2)+(1*4)=146
146 % 10 = 6
So 85185-24-6 is a valid CAS Registry Number.

85185-24-6SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 19, 2017

Revision Date: Aug 19, 2017

1.Identification

1.1 GHS Product identifier

Product name 3-[N-(tert-butoxycarbonyl)amino]pentanedioic acid

1.2 Other means of identification

Product number -
Other names 3-(N-Boc)pentanedioic acid

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:85185-24-6 SDS

85185-24-6Relevant academic research and scientific papers

IONIZABLE COMPOUNDS AND COMPOSITIONS AND USES THEREOF

-

Paragraph 0561; 0562, (2017/01/19)

This invention includes ionizable compounds, and compositions and methods of use thereof. The ionizable compounds can be used for making nanoparticle compositions for use in biopharmaceuticals and therapeutics. More particularly, this invention relates to compounds, compositions and methods for providing nanoparticles to encapsulate active agents, such as nucleic acid agents, and to deliver and distribute the active agents to cells, tissues, organs, and subjects.

Polypeptide formation by heating N-t-butyloxycarbonyl acidic amino acid derivatives

Munegumi,Qing Meng,Harada

, p. 4716 - 4722 (2014/12/10)

An acid labile N-protecting group for amino acids, t-butyloxycarbonyl (Boc) group has deprotected at elevated temperatures. The study describes an application of the lability on heating to synthesis of polypeptides from acidic amino acids. t-Butyloxycarbonyl-acidic amino acids (aspartic acid, glutamic acid and β-aminoglutaric acid) and their anhydrides were heated at the higher temperatures than their melting points. Anhydrides of t-butyloxycarbonyl-aspartic acid and t-butyloxycarbonyl-β-aminoglutaric acid gave polypeptides. Thermal analyses of the substrates clarified the pathway of the polypeptide formation.

2-CYANOPYRROLES AND THEIR ANALOGUES AS DDP-IV INHIBITORS

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Page/Page column 64, (2010/02/08)

The present invention relates to therapeutically active and selective inhibitors of the enzyme DPP-IV having the formula I: (I) The invention furthermore relates to pharmaceutical compositions comprising the compounds and the use of such compounds for the manufacture of medicaments for treating diseases that are associated with proteins which are subject to inactivation by DPP-IV, such as type 2 diabetes and obesity.

Thermal Syntheses of Polypeptides from N-Boc-Amino Acid(Aspartic Acid,β-Aminoglutaric Acid) Anhydrides

Munegumi, Toratane,Meng, Yan-Quing,Harada, Kaoru

, p. 1643 - 1646 (2007/10/02)

N-t-Butyloxycarbonyl-amino acid(aspartic acid:Asp, glutamic acid:Glu, β-aminoglutaric acid: β-Agl)anhydrides were deprotected upon heating at temperatures slightly higher than the melting points of these compounds and polypeptides were synthesized easily in high yield.

Potential antitumor agents. 45. Synthesis, DNA-binding interaction, and biological activity of triacridine derivatives

Atwell,Baguley,Wilmanska,Denny

, p. 69 - 74 (2007/10/02)

A series of amide-linked triacridines of varying interchromophore separation were synthesized as potential DNA trisintercalating agents. The correseponding diamide diacridines (lacking the central chromophore) were also prepared, and the DNA-binding and b

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