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1,2-Benzenedicarbonitrile, 3-hydroxy-6-(pentyloxy)- is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

75941-30-9

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75941-30-9 Usage

Structure

A derivative of benzenedicarbonitrile with a hydroxyl group and a pentyloxy side chain attached to the benzene ring

Structure

The compound is derived from benzenedicarbonitrile, which is a benzene ring with two cyano groups (CN) attached. It has a hydroxyl group (OH) and a pentyloxy side chain (C5H11O) attached to the benzene ring.

Usage

Commonly used in the synthesis of pharmaceuticals, dyes, and other organic compounds

Usage

The compound is used in the synthesis of various products, including pharmaceuticals, dyes, and other organic compounds.

Applications

Potential applications in the field of organic chemistry and drug development

Applications

Due to its unique structure and properties, the compound has potential applications in organic chemistry and drug development.

Safety

Handle with care due to potential health and environmental hazards

Safety

It is important to handle this chemical with care, as it may pose health and environmental risks if not properly managed.

Check Digit Verification of cas no

The CAS Registry Mumber 75941-30-9 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 7,5,9,4 and 1 respectively; the second part has 2 digits, 3 and 0 respectively.
Calculate Digit Verification of CAS Registry Number 75941-30:
(7*7)+(6*5)+(5*9)+(4*4)+(3*1)+(2*3)+(1*0)=149
149 % 10 = 9
So 75941-30-9 is a valid CAS Registry Number.

75941-30-9SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 17, 2017

Revision Date: Aug 17, 2017

1.Identification

1.1 GHS Product identifier

Product name 3-hydroxy-6-pentoxybenzene-1,2-dicarbonitrile

1.2 Other means of identification

Product number -
Other names -

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:75941-30-9 SDS

75941-30-9Downstream Products

75941-30-9Relevant academic research and scientific papers

Assemblies of Boron Dipyrromethene/Porphyrin, Phthalocyanine, and C60 Moieties as Artificial Models of Photosynthesis: Synthesis, Supramolecular Interactions, and Photophysical Studies

Chen, Xiao-Fei,El-Khouly, Mohamed E.,Ohkubo, Kei,Fukuzumi, Shunichi,Ng, Dennis K. P.

, p. 3862 - 3872 (2018/03/21)

A series of light-harvesting conjugates based on a zinc(II) phthalocyanine core with either two or four boron dipyrromethene (BODIPY) or porphyrin units have been synthesized and characterized. The conjugation of BODIPY/porphyrin units can extend the absorptions of the phthalocyanine core to cover most of the visible region. Upon addition of an imidazole-substituted C60 (C60Im), it can axially bind to the zinc(II) center of the phthalocyanine core through metal–ligand interactions. The resulting complexes form photosynthetic antenna-reaction center mimics in which the BODIPY/porphyrin units serve as the antennas to capture the light and transfer the energy to the phthalocyanine core by efficient excitation energy transfer. The excited phthalocyanine is then quenched by the axially bound C60Im moiety by electron transfer, which has been supported by computational studies. The photoinduced processes of the assemblies have been studied in detail by various steady-state and time-resolved spectroscopic methods. By femtosecond transient absorption spectroscopic studies, the lifetimes of the charge-separated state of the bis(BODIPY) and bis(porphyrin) systems have been determined to be 3.2 and 4.0 ns, respectively.

2,3-DICYANOHYDROQUINONE DERIVATIVE LIQUID CRYSTALS HAVING STRONG NEGATIVE DIELECTRIC ANISOTROPY.

Inukai,Furukawa,Inoue,Terashima

, p. 109 - 118 (2007/10/02)

Three groups of liquid crystalline derivatives of 2,3-dicyanohydroquinone were synthesized. The dielectric anisotropy values, DELTA epsilon s, for these compounds were estimated to be around minus 20 by extrapolation. Some basic evaluations of these compo

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