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5281-84-5

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5281-84-5 Usage

Physical state

Yellow crystalline solid

Structure

Benzonitrile group attached to a substituent containing a chloro-nitrophenyl group and an amino group

Potential applications

Pharmaceutical and materials science

Building block

Due to the presence of chloro and nitro groups

Biological activity

Possible, due to the presence of an amino group

Precursor for new compounds

Potentially used in the development of new pharmaceuticals or agrochemicals

Check Digit Verification of cas no

The CAS Registry Mumber 5281-84-5 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 5,2,8 and 1 respectively; the second part has 2 digits, 8 and 4 respectively.
Calculate Digit Verification of CAS Registry Number 5281-84:
(6*5)+(5*2)+(4*8)+(3*1)+(2*8)+(1*4)=95
95 % 10 = 5
So 5281-84-5 is a valid CAS Registry Number.
InChI:InChI=1/C14H8ClN3O2/c15-13-6-5-12(18(19)20)7-11(13)9-17-14-4-2-1-3-10(14)8-16/h1-7,9H/b17-9+

5281-84-5SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 19, 2017

Revision Date: Aug 19, 2017

1.Identification

1.1 GHS Product identifier

Product name 2-[(2-chloro-5-nitrophenyl)methylideneamino]benzonitrile

1.2 Other means of identification

Product number -
Other names 2-({2-chloro-5-nitrobenzylidene}amino)benzonitrile

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:5281-84-5 SDS

5281-84-5Downstream Products

5281-84-5Relevant articles and documents

Selection of surfactant-modified lipases for interesterification of triglyceride and fatty acid

Mogi, Ken-Ichi,Nakajima, Mitsutoshi

, p. 1505 - 1512 (2007/10/03)

Interesterification of tripalmitin and stearic acid in n-hexane was investigated with surfactant-modified lipases. Various kinds of lipases and surfactants were screened for high interesterification activity of the modified lipases. The modified-lipase activity was influenced by both the lipases and the hydrophile-lipophile balance value and fatty acid group of the surfactants. The modified lipase obtained from Rhizopus japonicus with sorbitan monostearate as surfactant had the highest activity in the n-hexane system. The interesterification activity of the selected modified lipase in molten substrates at 75°C without solvents was the same as that in the n-hexane system at 40°C.

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