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Phenol, 4-[(4-decylphenyl)azo]- is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

620180-53-2

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620180-53-2 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 620180-53-2 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 6,2,0,1,8 and 0 respectively; the second part has 2 digits, 5 and 3 respectively.
Calculate Digit Verification of CAS Registry Number 620180-53:
(8*6)+(7*2)+(6*0)+(5*1)+(4*8)+(3*0)+(2*5)+(1*3)=112
112 % 10 = 2
So 620180-53-2 is a valid CAS Registry Number.

620180-53-2SDS

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 4-[(4-decylphenyl)hydrazinylidene]cyclohexa-2,5-dien-1-one

1.2 Other means of identification

Product number -
Other names Phenol,4-[(4-decylphenyl)azo]

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:620180-53-2 SDS

620180-53-2Relevant articles and documents

Containing azo phenyl the xylosides and its preparation method and application

-

Paragraph 01345-0136, (2017/05/02)

The invention belongs to the field of catalytic reaction engineering, and particularly relates to synthetic glucoside containing an azobenzene group, and application of the glucoside serving as an ultraviolet controlled-release material. The glucoside containing an azobenzene group has a structure as shown in Formula (I). The glucoside containing an azobenzene group can be used for preparation of ultraviolet sensitive liposome, and has favorable structural stability, biological targeting property, biocompatibility and in-vivo degradability.

Liquid-crystalline polymorphism of symmetrical azobananas: Bis(4-(4-alkylphenyl)azophenyl) 2-nitroisophtalates

Zygadlo,Dardas,Nowicka,Hofmann,Galewski

, p. 283 - 291 (2011/08/02)

In this paper we present a series of novel compounds, bis(4-(4-alkylphenyl) azophenyl) 2-nitroisophtalates, which exhibit nematic and banana-type liquidcrystalline phases. The alkyl chain length varies from 1 to 18 carbons. The first ten members of this series exhibit nematic phase. The last eleven compounds exhibit banana-type liquid crystalline phases. The propyl and pentyl derivatives have extra second type of banana mesophase. Copyright Taylor & Francis Group, LLC.

Photo-induced molecular-recognition-mediated adhesion of giant vesicles

Mansfeld, Friederike M.,Feng, Guoqiang,Otto, Sijbren

experimental part, p. 4289 - 4295 (2009/12/06)

Few methods currently exist for controlling vesicle-vesicle adhesion. We now report a new system, based upon a multivalent guest and an amphiphilic receptor with a photo-isomerisable anchor that can be incorporated into lipid vesicles of different sizes.

A convenient synthesis of novel mercapto-ended azobenzene derivatives

Haiying, Li,Zhongfan, Liu

, p. 3779 - 3785 (2007/10/03)

Treatment of the product from the Diazo-Coupling reaction of p- alkylaniline with 1,3-dibromopropane in THF affords intermediate compounds n- C(n)H(2n+1)AzoO(CH2)(m)Br. Subsequent treatment of these intermediate with thiourea in ethanol at refl

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