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17448-55-4

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17448-55-4 Usage

General Description

[(1S,2R)-2-nitrocyclohexyl]benzene is a chemical compound with the molecular formula C12H13NO2. It consists of a benzene ring attached to a cyclohexane ring, with a nitro group attached to the cyclohexane ring. The stereochemistry of the compound is described by the (1S,2R) configuration, indicating the spatial arrangement of its atoms. [(1S,2R)-2-nitrocyclohexyl]benzene is used in organic synthesis and chemical research, and its properties make it useful in the development of new materials, pharmaceuticals, and agrochemicals. It is important to handle and use this chemical with care, as it may pose health hazards and should be stored and disposed of properly in accordance with safety guidelines.

Check Digit Verification of cas no

The CAS Registry Mumber 17448-55-4 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 1,7,4,4 and 8 respectively; the second part has 2 digits, 5 and 5 respectively.
Calculate Digit Verification of CAS Registry Number 17448-55:
(7*1)+(6*7)+(5*4)+(4*4)+(3*8)+(2*5)+(1*5)=124
124 % 10 = 4
So 17448-55-4 is a valid CAS Registry Number.

17448-55-4SDS

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 cis-1-Phenyl-2-nitrocyclohexan

1.2 Other means of identification

Product number -
Other names Icosylamine

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:17448-55-4 SDS

17448-55-4Relevant articles and documents

Deoxycholic acid-derived biaryl phosphites as versatile and enantioselective ligands in the rhodium-catalyzed conjugate addition of arylboronic acids to nitroalkenes

Jumde, Varsha R.,Iuliano, Anna

, p. 3475 - 3483 (2013/12/04)

A highly enantioselective conjugate addition of arylboronic acids to cyclic as well as acyclic aromatic and aliphatic nitroalkenes is presented. The rhodium complexes obtained from deoxycholic acid-derived binaphthyl and flexible biphenyl phosphites showed good activity as well as very high enantioselectivity (ee up to 99%) in the conjugated addition even in the presence of challenging substrates such as 1-nitrocyclohexene or aliphatic acyclic nitroalkenes. Copyright

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