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111709-87-6

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111709-87-6 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 111709-87-6 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,1,1,7,0 and 9 respectively; the second part has 2 digits, 8 and 7 respectively.
Calculate Digit Verification of CAS Registry Number 111709-87:
(8*1)+(7*1)+(6*1)+(5*7)+(4*0)+(3*9)+(2*8)+(1*7)=106
106 % 10 = 6
So 111709-87-6 is a valid CAS Registry Number.

111709-87-6SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 17, 2017

Revision Date: Aug 17, 2017

1.Identification

1.1 GHS Product identifier

Product name amino-1 vinyl-1 cyclohexane

1.2 Other means of identification

Product number -
Other names 1-Ethenylcyclohexylamin

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:111709-87-6 SDS

111709-87-6Relevant articles and documents

Stable Zero-Valent Nickel Nanoparticles in Glycerol: Synthesis and Applications in Selective Hydrogenations

Reina, Antonio,Favier, Isabelle,Pradel, Christian,Gómez, Montserrat

, p. 3544 - 3552 (2018/08/01)

Small (mean diameter, ca. 1.2 nm) and well-dispersed zero-valent nickel nanoparticles (NiNPs) stabilized by cinchona-based alkaloids and TPPTS (tris(3-sulfophenyl)phosphine trisodium salt), were synthesized from the organometallic precursor [Ni(cod)2] in neat glycerol under hydrogen pressure. NiNPs were fully characterized ((HR)-TEM, EDX, XPS, XRD, IR, magnetization), both at solid state and directly from the corresponding colloidal solutions in glycerol due to its negligible vapour pressure. NiNPs dispersed in glycerol were applied in hydrogenation reactions, in particular in semihydrogenation of alkynes to give (Z)-alkenes under satisfactory conditions (3 bar H2, 1 mol% Ni, 100 °C), showing remarkable activity and selectivity. The catalytic phase was recycled at least ten times without loss of activity, affording in each case metal-free organic products. Other functional groups such as nitro, nitrile and formyl groups were efficiently hydrogenated to the corresponding anilines, benzylamines and benzylalcohols respectively (77–95% yields). (Figure presented.).

Amination of Olefinic Compounds with Bis(2,2,2-trichloroethyl) Azodicarboxylate

Leblanc, Yves,Zamboni, Robert,Bernstein, Michael A.

, p. 1971 - 1972 (2007/10/02)

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