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Cyclohexanamine, N-cyclopentylidene- is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

42908-34-9

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42908-34-9 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 42908-34-9 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 4,2,9,0 and 8 respectively; the second part has 2 digits, 3 and 4 respectively.
Calculate Digit Verification of CAS Registry Number 42908-34:
(7*4)+(6*2)+(5*9)+(4*0)+(3*8)+(2*3)+(1*4)=119
119 % 10 = 9
So 42908-34-9 is a valid CAS Registry Number.

42908-34-9SDS

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 N-cyclohexylcyclopentanimine

1.2 Other means of identification

Product number -
Other names N-cyclohexyl-N-cyclopentylidenamine

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:42908-34-9 SDS

42908-34-9Relevant academic research and scientific papers

Synthesis of pyridines and pyrazines using an intramolecular hydroamination-based reaction sequence

Rizk, Toni,Bilodeau, Eric J.-F.,Beauchemin, Andre M.

supporting information; experimental part, p. 8325 - 8327 (2010/01/16)

A management issue! Various pyridines and pyrazines can be efficiently accessed from simple acyclic precursors using an intramolecular hydroamination/isomerization/aromatization sequence (see scheme). ρ-Toluenesulfonic acid (2 mol%) is used to catalyze this novel alkyne annulation, in which the oxime group allows for a subsequent redoxneutral aromatization step to occur.

Intramolecular ene and related reactions, Part 9. Photochemically induced synthesis of allylsilane carbaldehydes

Tietze,Wunsch

, p. 985 - 990 (2007/10/02)

Allylsilane carbaldehydes are valuable substrates for the tandem Koevenagel allylsilane and iminium cyclization. They can easily be prepared by a photochemical α-cleavage of cyclic ketones bearing a trimethylsilylmethyl group in the α-position (Norrish Ty

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