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114568-55-7

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114568-55-7 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 114568-55-7 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,1,4,5,6 and 8 respectively; the second part has 2 digits, 5 and 5 respectively.
Calculate Digit Verification of CAS Registry Number 114568-55:
(8*1)+(7*1)+(6*4)+(5*5)+(4*6)+(3*8)+(2*5)+(1*5)=127
127 % 10 = 7
So 114568-55-7 is a valid CAS Registry Number.

114568-55-7SDS

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 N-hexyl-2-methoxy-4-nitroaniline

1.2 Other means of identification

Product number -
Other names Benzenamine,N-hexyl-2-methoxy-4-nitro

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:114568-55-7 SDS

114568-55-7Relevant articles and documents

COMPOUNDS AS PPAR BETA/DELTA INHIBITORS FOR TREATING PPAR BETA/DELTA-MEDIATED DISEASES

-

Paragraph 0121; 0122, (2015/02/18)

The present invention concerns substances which act as selective ligands of nuclear receptors of the PPAR beta/delta subtype and which can be used for the treatment of PPAR beta/delta-mediated diseases. The substances of this invention act as inhibitors of PPAR beta/delta receptors.

ON THE REGIOSELECTIVITY OF THE NUCLEOPHILIC AROMATIC PHOTOSUBSTITUTION. THE PHOTOREACTION OF 4-NITROVERATROLE WITH n-HEXYLAMINE.

Cantos, Albert,Marquet, Jorge,Moreno-Manas, Marcial

, p. 4191 - 4194 (2007/10/02)

4-Nitroveratrole is photosubstituted with n-hexylamine giving rise to two isomeric anilines, N-hexyl-2-methoxy-5-nitroaniline and N-hexyl-2-methoxy-4-nitroaniline.Mechanistic evidence indicates that the first is produced in an SN2Ar* reaction through singlet and triplet excited states, whereas the second arises from a radical ion pair via electron transfer from the amine to a triplet excited state.

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