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14381-98-7

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14381-98-7 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 14381-98-7 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 1,4,3,8 and 1 respectively; the second part has 2 digits, 9 and 8 respectively.
Calculate Digit Verification of CAS Registry Number 14381-98:
(7*1)+(6*4)+(5*3)+(4*8)+(3*1)+(2*9)+(1*8)=107
107 % 10 = 7
So 14381-98-7 is a valid CAS Registry Number.

14381-98-7SDS

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 (2,5-dimethylphenyl)-(2,5-dimethylphenyl)imino-oxidoazanium

1.2 Other means of identification

Product number -
Other names 2.5.2'.5'-Tetramethyl-azoxybenzol

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:14381-98-7 SDS

14381-98-7Relevant articles and documents

Room temperature selective reduction of nitrobenzene to azoxybenzene over magnetically separable urchin-like Ni/Graphene nanocomposites

Pahalagedara, Madhavi N.,Pahalagedara, Lakshitha R.,He, Junkai,Miao, Ran,Gottlieb, Becca,Rathnayake, Dinithi,Suib, Steven L.

, p. 41 - 48 (2016/02/12)

Magnetically recyclable Ni/Graphene (Ni/G) nanocomposites were synthesized via an in situ reduction growth process for selective reduction of nitroarenes into corresponding azoxybenzene at room temperature and at atmospheric pressure. Here, hydrazine hydrate (N2H4H2O) is used as the reducing agent which generates harmless by-products such as N2 and water. The catalyst, when used under controlled reaction conditions, exhibits a 100% conversion and selectivity to the target product without the use of any external additives (turnover number 36.2). Under the optimized conditions, a variety of structurally different nitroarenes were selectively transformed to their corresponding azoxy products in high conversions. Furthermore, a high stability and recyclability of the catalyst were also observed under the investigated conditions (93% conversion, 100% selectivity after the 4th reuse).

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