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36422-63-6

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36422-63-6 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 36422-63-6 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 3,6,4,2 and 2 respectively; the second part has 2 digits, 6 and 3 respectively.
Calculate Digit Verification of CAS Registry Number 36422-63:
(7*3)+(6*6)+(5*4)+(4*2)+(3*2)+(2*6)+(1*3)=106
106 % 10 = 6
So 36422-63-6 is a valid CAS Registry Number.

36422-63-6SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 15, 2017

Revision Date: Aug 15, 2017

1.Identification

1.1 GHS Product identifier

Product name 2,2'-(1,2-ETHENEDIYLDI-4,1-PHENYLENE)BISBENZOXAZOLE

1.2 Other means of identification

Product number -
Other names 4,4'-Bis-<2,4-dihydroxy-phenylazo>-biphenyl

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:36422-63-6 SDS

36422-63-6Downstream Products

36422-63-6Relevant articles and documents

Production process of fluorescent whitening agent OB-1

-

Paragraph 0030; 0037; 0046-0055, (2021/03/11)

The invention relates to a production process of a fluorescent whitening agent OB-1. The production process specifically comprises the following steps: 1, carrying out condensation reaction on p-toluic acid and o-aminophenol to generate 4-methyl phenyl benzoxazole; 2, carrying out distillation treatment after the condensation reaction is finished, and collecting a main fraction 4-methyl intermediate; 3, adding methanol into the main fraction, keeping the temperature at 60 DEG C for 6 hours, cooling to 10 DEG C, centrifugally filtering, drying, and transferring into a vulcanization synthesis kettle; 4, carrying out a vulcanization synthesis reaction on the 4-methyl intermediate to generate OB-1, rinsing with xylene, repeatedly washing with xylene, and drying the xylene by distillation to obtain a dried OB-1 crude product; 5, adding trichlorobenzene, the OB-1 crude product and activated carbon into a refining kettle to refine OB-1; and 6, pulping and washing OB-1 with methanol, carryingout centrifugal separation, and drying a filtering cake to obtain the OB-1 product. The method is environmentally friendly, safe and high in yield.

Synthesis and spectral-luminescence properties of 4,4′-di(2-oxazolyl)-stilbenes and 4,4′-di(2-oxazolyl)tolans

Vernigor,Shalaev,Luk'yanets

, p. 328 - 332 (2007/10/02)

A new method is proposed for the synthesis of 4,4′-di(2-oxazolyl)stilbenes and 4,4′-di(2-oxazolyl) tolans by condensation of oxazolyl-substituted benzyl bromides or benzal dibromides under the influence of strong bases (KOH, potassium tertbutoxide) in dipolar aprotic solvents [dimethylformamide (DMF) and dimethyl sulfoxide (DMSO)]. The synthesized compounds luminesce intensely over the spectral range 386-492 nm.

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