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4050-48-0

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4050-48-0 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 4050-48-0 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 4,0,5 and 0 respectively; the second part has 2 digits, 4 and 8 respectively.
Calculate Digit Verification of CAS Registry Number 4050-48:
(6*4)+(5*0)+(4*5)+(3*0)+(2*4)+(1*8)=60
60 % 10 = 0
So 4050-48-0 is a valid CAS Registry Number.

4050-48-0SDS

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-nitrocyclohexanol

1.2 Other means of identification

Product number -
Other names 2-Nitro-cyclohexanol-(1)

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:4050-48-0 SDS

4050-48-0Relevant articles and documents

Synthesis and characterization of a novel nanomagnetic phase-transfer catalyst and its application to regioselective synthesis of β-azido and β-nitro alcohols in water

Ayashi,Fallah-Mehrjardi,Kiasat

, p. 846 - 852 (2017/08/02)

Immobilization of polyethylene glycol-substituted 1-methylimidazolium bromide on the surface of magnetic Fe3O4 nanoparticles through hexane-1,6-diyldicarbamate linker afforded a powerful and reusable heterogeneous phase-transfer cata

Efficient kinetic bioresolution of 2-nitrocyclohexanol

Milner, Sinead E.,Brossat, Maude,Moody, Thomas S.,Elcoate, Curtis J.,Lawrence, Simon E.,Maguire, Anita R.

experimental part, p. 1011 - 1016 (2010/08/22)

The kinetic bioresolution of 2-nitrocyclohexanol 1 was investigated by screening a range of hydrolases both for enantioselective transesterification and for enantioselective hydrolysis of the corresponding acetate. By appropriate choice of biocatalyst and conditions, both enantiomers of cis and trans 2-nitrocyclohexanol 1 can be accessed in enantiopure form.

Micellar media for the efficient ring opening of epoxides with CN-, N3-, NO3-, NO2-, SCN-, Cl- and Br- catalyzed with Ce(OTf)4

Iranpoor, Nasser,Firouzabadi, Habib,Shekarize, Marzieh

, p. 724 - 727 (2007/10/03)

Micellar media are introduced for the efficient ring opening of epoxides with sodium salts of nucleophiles such as CN, N3-, NO3-, NO2, SCN, Br and Cl-, catalyzed with Ce(OTf)4. This method is an efficient procedure for the synthesis of different β-substituted alcohols under mild reaction conditions. The reaction with SCN- is an easy procedure for the high yielding preparation of epoxy sulfides.

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