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1H-Isoindole-1,3(2H)-dione, 2-(10-undecenyl)- is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

88124-95-2

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88124-95-2 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 88124-95-2 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 8,8,1,2 and 4 respectively; the second part has 2 digits, 9 and 5 respectively.
Calculate Digit Verification of CAS Registry Number 88124-95:
(7*8)+(6*8)+(5*1)+(4*2)+(3*4)+(2*9)+(1*5)=152
152 % 10 = 2
So 88124-95-2 is a valid CAS Registry Number.

88124-95-2SDS

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 2-undec-10-enylisoindole-1,3-dione

1.2 Other means of identification

Product number -
Other names 1-phthalimidylundec-10-ene

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:88124-95-2 SDS

88124-95-2Relevant academic research and scientific papers

ARYL, HETEROARYL, AND HETEROCYCLIC COMPOUNDS FOR TREATMENT OF MEDICAL DISORDERS

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Paragraph 0595, (2017/03/14)

Compounds, methods of use, and processes for making inhibitors of complement Factor D comprising Formula I, or a pharmaceutically acceptable salt or composition thereof wherein R12 or R13 on the A group is an aryl, heteroaryl or heterocycle (R32) are provided. The inhibitors of Factor D described herein reduce the excessive activation of complement.

ALKYNE COMPOUNDS FOR TREATMENT OF IMMUNE AND INFLAMMATORY DISORDERS

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Paragraph 0566; 0660; 0661, (2017/03/14)

Compounds, methods of use, and processes for making inhibitors of complement Factor D are provided comprising Formula I, I" and I'" or a pharmaceutically acceptable salt or composition thereof. The inhibitors described herein target Factor D and inhibit or regulate the complement cascade. The inhibitors of Factor D described herein reduce the excessive activation of complement.

FLUORESCENT LABELED INHIBITORS

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Sheet 10, (2015/09/28)

Provided herein are a series of fluorescently labeled phosphonate and phosphate compounds such as can be used for affinity probes to detect certain enzymes including lipases. Also provided are methods of making and using such compounds.

Oligoamide duplexes as organogelators

Cao, Ruikai,Zhou, Jingjing,Wang, Wei,Feng, Wen,Li, Xianghui,Zhang, Penghui,Deng, Pengchi,Yuan, Lihua,Gong, Bing

supporting information; experimental part, p. 2958 - 2961 (2010/09/15)

Oligoamide duplexes carrying multiple alkyl side chains were found to serve as gelators for aromatic solvents. The double-stranded backbone was essential for the hierarchical self-assembly of the molecular duplex into fibers of high aspect ratios. The demonstrated gelating abilities may be extended to a large family of analogous H-bonded duplexes having different H-bonding sequences, leading to a unique platform for developing a diverse variety of potential gelators based on a supramolecular and/or a dynamic covalent approach.

Siloxanes with pendent naphthalene diimides: Synthesis and fluorescence quenching

Ganesan, Palaniswamy,Van Lagen, Barend,Marcelis, Antonius T. M.,Sudholter, Ernst J. R.,Zuilhof, Han

, p. 2296 - 2300 (2008/02/05)

Cyclic siloxanes with pendent naphthalene diimide groups were synthesized via hydrosilylation to form amorphous electron-accepting compounds. Photophysical measurements and >99.9% fluorescence quenching of well-known p-type polymers by the siloxanes demonstrate that these siloxanes form a new class of highly efficient n-type materials that provide some control over intermolecular interactions.

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