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Diazene, (4-methoxy-1-naphthalenyl)(4-nitrophenyl)- is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

36853-74-4

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36853-74-4 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 36853-74-4 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 3,6,8,5 and 3 respectively; the second part has 2 digits, 7 and 4 respectively.
Calculate Digit Verification of CAS Registry Number 36853-74:
(7*3)+(6*6)+(5*8)+(4*5)+(3*3)+(2*7)+(1*4)=144
144 % 10 = 4
So 36853-74-4 is a valid CAS Registry Number.

36853-74-4SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 16, 2017

Revision Date: Aug 16, 2017

1.Identification

1.1 GHS Product identifier

Product name (4-methoxynaphthalen-1-yl)-(4-nitrophenyl)diazene

1.2 Other means of identification

Product number -
Other names (4-methoxy-[1]naphthyl)-(4-nitro-phenyl)-diazene

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:36853-74-4 SDS

36853-74-4Downstream Products

36853-74-4Relevant academic research and scientific papers

Photochromic Properties of Unsymmetric Mono- and Bis(phenylazo)naphthalenes

Yoshida, Katsuhira,Koujiri, Tetsunao,Horii, Taeko,Kubo, Yuji

, p. 1658 - 1664 (2007/10/02)

To utilize the reversible photochromic system of phenylazonaphthalenes in a design of functional molecule, the photochromic behaviors of various substituted phenylazonaphthalenes have been investigated.Introduction of substituents onto ortho positions with respect to the azo group retarded the rate of thermal cis-to-trans isomerization.The retardation effects were greatly dependent on both the number and position of the ortho substituents.To investigate the retardation effects of ortho substituents, the activation parameters were determined; the results suggest that the steric hindrance among the ortho substituents and the two nitrogen lone pairs of the azo group becomes far more severe in an inversional transition-state than in the ground cis-state, which leads to the remarkable slow cis-to-trans isomerization.On the basis of the kinetic data of various phenylazonaphthalenes, the complicated isomerization behaviors of unsymmetric bis(phenylazo)naphthalenes have been elucidated.

A FACILE IN-SITU DIAZO COUPLING REACTIONS UNDER TWO-PHASE CONDITIONS CATALYZED BY TETRAKISBORATE ION

Iwamoto, Hidetoshi,Sonoda, Takaaki,Kobayashi, Hiroshi

, p. 4703 - 4706 (2007/10/02)

In-situ diazo-coupling and N- and C-nitrosations under CH2Cl2-aq.H2SO4 two-phase systems have proved to be catalyzed by TFPB ion.

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