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121086-17-7

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121086-17-7 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 121086-17-7 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,2,1,0,8 and 6 respectively; the second part has 2 digits, 1 and 7 respectively.
Calculate Digit Verification of CAS Registry Number 121086-17:
(8*1)+(7*2)+(6*1)+(5*0)+(4*8)+(3*6)+(2*1)+(1*7)=87
87 % 10 = 7
So 121086-17-7 is a valid CAS Registry Number.

121086-17-7SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 19, 2017

Revision Date: Aug 19, 2017

1.Identification

1.1 GHS Product identifier

Product name N-cyclohexyl-3-nitroaniline

1.2 Other means of identification

Product number -
Other names Benzenamine,N-cyclohexyl-3-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:121086-17-7 SDS

121086-17-7Downstream Products

121086-17-7Relevant articles and documents

Two Component Recyclable Heterogeneous Catalyst, Process for Preparation Thereof and its Use for Preparation of Amines

-

Page/Page column 6-7, (2012/01/13)

The invention describes the development of highly efficient, recyclable two component system, CuAl-hydrotalcite/rac 1,1′-Binaphthalene-2,2′-diol catalytic system for the N-alkylation of electron deficient aryl chlorides in presence of potassium carbonate as a base at room temperature in 3-6 h, wherein the process is provided for the preparation of various secondary amines via C—N coupling reaction of aliphatic amines(aliphatic open chain, acyclic, benzyl amines and heterocyclic amines) with various aryl chlorides.

CuI nanoparticles for C-N and C-O cross coupling of heterocyclic amines and phenols with chlorobenzenes

Sreedhar,Arundhathi,Reddy, P. Linga,Kantam, M. Lakshmi

supporting information; experimental part, p. 7951 - 7954 (2010/01/16)

(Chemical Equation Presented) Employing CuI nanoparticles as an efficient catalyst for the cross-coupling reactions of various N/O nucleophilic reagents with aryl chlorides could be successfully carried out under mild conditions in the absence of both the ligands and strong bases. A variety of products including N-arylimidazoles and aryl ethers were synthesized in good to excellent yields. 2009 American Chemical Society.

CuBr/rac-BINOL-catalyzed N-arylations of aliphatic amines at room temperature

Jiang, Deshou,Fu, Hua,Jiang, Yuyang,Zhao, Yufen

, p. 672 - 674 (2007/10/03)

We have developed an efficient and readily available catalyst system CuBr/racemic BINOL ( 1,1′-binaphthyl-2,2′-diol) that catalyzes N-arylation of aliphatic amines at room temperature, and this inexpensive catalyst system is of high selectivity and tolerance toward various functional groups in the substrates.

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