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Cyclohexanamine, N-(1-methylheptylidene)- is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

53626-91-8

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53626-91-8 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 53626-91-8 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 5,3,6,2 and 6 respectively; the second part has 2 digits, 9 and 1 respectively.
Calculate Digit Verification of CAS Registry Number 53626-91:
(7*5)+(6*3)+(5*6)+(4*2)+(3*6)+(2*9)+(1*1)=128
128 % 10 = 8
So 53626-91-8 is a valid CAS Registry Number.

53626-91-8SDS

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 cyclohexyl-(1-methyl-heptylidene)-amine

1.2 Other means of identification

Product number -
Other names N-(1-methylheptylidene)cyclohexylamine

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:53626-91-8 SDS

53626-91-8Relevant academic research and scientific papers

A silica-supported titanium catalyst for heterogeneous hydroamination and multicomponent coupling reactions

Aldrich, Kelly E.,Odom, Aaron L.

, p. 11352 - 11360 (2019/08/07)

Highly dehydrated silica gel, SiO2700, gave a material with a total surface hydroxyl density of 0.31 ± 0.05 mmol g-1, 0.9 ± 0.1 Si-OH sites per nm2. Treatment of this material with Ti(NMe2)4/sub

Double hydroacylation reactions of acyclic and cyclic α,β- unsaturated aldehydes

Cha, Kyung-Mi,Lee, Hyejeong,Park, Jung-Woo,Lee, Yura,Jo, Eun-Ae,Jun, Chul-Ho

supporting information; experimental part, p. 1926 - 1930 (2011/10/17)

Double or quits? double hydroacylation reactions of acyclic and cyclic α,β-unsaturated aldehydes with olefins afford ketone and diketone products, respectively. Enantiomers are formed whose absolute configurations are controlled by the order of alkene addition.

Alkynylmercury Chloride or Acetate as Intermediates in the Mercury(II) Salt-promoted Addition of Aliphatic and Aromatic Amines to Terminal Acetylenes

Barluenga, Jose,Aznar, Fernando,Liz, Ramon,Rodes, Rosa

, p. 1087 - 1091 (2007/10/02)

Arylaminomercuriation of terminal acetylenes has been carried out with aliphatic amines to yield amines and enamines.Phenylethynylmercury chloride is shown to be an intermediate in the mercury(II) salt-promoted addition of aliphatic and aromatic amines to terminal alkynes.

Synthesis of 1,3,5-Trialkylbenzenes from Anils of Methyl Alkyl Ketones

Layer, Robert W.

, p. 4552 - 4555 (2007/10/02)

Besides the previously observed 2,2,4-trialkyl-1,2-dihydroquinolines, a mixture of 1,3,5-trialkylbenzenes and 1-methyl-2,3,5-trialkylbenzenes was obtained in up to 50percent yields when methyl alkyl ketones, aniline, and an acidic catalyst, such as hydrogen chloride, were heated to 180 deg C and the water was removed as formed.The reaction is thought to proceed through an α,β,γ,δ-unsaturated anil intermediate, but the corresponding α,β,γ,δ-unsaturated imines and aliphatic amines did not give trialkylbenzenes.

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