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4-Hexylcyclohexan-1-one is an organic compound with the molecular formula C12H22O. It is a cyclic ketone, characterized by a six-membered cyclohexane ring with a hexyl chain attached to the fourth carbon and a carbonyl group (C=O) at the first carbon. This chemical is known for its unique aroma and is often used in the fragrance industry to create floral, fruity, and green scent profiles. It can be found in various natural sources, such as fruits and flowers, and is also synthesized for commercial use. Due to its pleasant scent, 4-hexylcyclohexan-1-one is a valuable component in the creation of perfumes, cosmetics, and other fragranced products.

5441-57-6

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5441-57-6 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 5441-57-6 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 5,4,4 and 1 respectively; the second part has 2 digits, 5 and 7 respectively.
Calculate Digit Verification of CAS Registry Number 5441-57:
(6*5)+(5*4)+(4*4)+(3*1)+(2*5)+(1*7)=86
86 % 10 = 6
So 5441-57-6 is a valid CAS Registry Number.
InChI:InChI=1/C12H22O/c1-2-3-4-5-6-11-7-9-12(13)10-8-11/h11H,2-10H2,1H3

5441-57-6SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 19, 2017

Revision Date: Aug 19, 2017

1.Identification

1.1 GHS Product identifier

Product name 4-hexylcyclohexan-1-one

1.2 Other means of identification

Product number -
Other names 4-n-Hexyl-cyclohexanon

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:5441-57-6 SDS

5441-57-6Relevant academic research and scientific papers

SUBSTITUTED BICYCLIC COMPOUNDS

-

Page/Page column 162, (2016/03/13)

Disclosed are compounds of Formulas (I), (II), (III), (IV), and (V) and/or a salt thereof, wherein R1 is OH or OP(O)(OH)2, and X1, X2, X3, R2, R2a, Ra, Rb, and Rc are defined herein. Also disclosed are methods of using such compounds as selective agonists for G protein coupled receptor S1P1, and pharmaceutical compositions comprising such compounds. These compounds are useful in treating, preventing, or slowing the progression of diseases or disorders in a variety of therapeutic areas, such as autoimmune diseases and vascular disease.

Relative Molecular Mass Information from Aliphatic Nitro Compounds: a Chemical Ionization Study

Ballantine, James A.,Barton, Jonathan D.,Carter, James F.,Davies, Jeremy P.,Smith, Keith,et al.

, p. 1 - 5 (2007/10/02)

The mass spectra of a number of aliphatic nitro compounds have been studied using electron ionization (EI) and a variety of chemical ionization (CI) techniques in attempts to obtain relative molecular mass information.The use of positive ion ammonia chemical ionization techniques gave very satisfactory results, providing abundant + ions, not only from both primary and secondary nitro compounds, but also from the much more labile tertiary nitro compounds.However, the use of methane and isobutane positive ion CI or EI conditions resulted in facile fragmentation with little relative molecular mass information being made available.Negative ion CI using methane, isobutane or ammonia as moderating gases all gave abundant - ions with primary and secondary nitro compounds but at much reduced sensitivity.

Aliphatic Liquid Crystals, 2. Some Nematic Derivatives of all-trans-Perhydrophenanthrene

Sucrow, Wolfgang,Minas, Hermann,Stegemeyer, Horst,Geschwinder, Peter,Murawski, Hans-Ruediger,Krueger, Carl

, p. 3332 - 3349 (2007/10/02)

A stereoselective synthesis of the all-trans-7-alkylperhydro-2-phenanthrenols 15a-f in 11 steps and 28 liquid crystalline esters 16 of 15a-f are described, additionally some further derivatives of 7-alkylperhydro-2-phenanthrenol.An X-ray structure analysis of ester 16ec is reported.

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