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3-Cyclohexene-1-carboxaldehyde, 2,2,4-trimethyl- is an organic compound with the molecular formula C10H16O. It is a colorless to pale yellow liquid with a strong, pungent odor. This aldehyde is a cyclic structure with a six-membered carbon ring, featuring a carbonyl group at the 1-position and a double bond between the 3rd and 4th carbon atoms. The molecule also contains three methyl groups attached to the 2nd, 2nd, and 4th carbon atoms, respectively. 3-Cyclohexene-1-carboxaldehyde, 2,2,4-trimethyl- is used as a fragrance ingredient in various applications, such as perfumes, cosmetics, and household products, due to its pleasant, fruity, and floral scent. It is also known as 2,2,4-trimethyl-3-cyclohexene-1-carboxaldehyde or simply as "TMCHC."

1726-47-2

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1726-47-2 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 1726-47-2 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 1,7,2 and 6 respectively; the second part has 2 digits, 4 and 7 respectively.
Calculate Digit Verification of CAS Registry Number 1726-47:
(6*1)+(5*7)+(4*2)+(3*6)+(2*4)+(1*7)=82
82 % 10 = 2
So 1726-47-2 is a valid CAS Registry Number.
InChI:InChI=1/C10H16O/c1-8-4-5-9(7-11)10(2,3)6-8/h6-7,9H,4-5H2,1-3H3

1726-47-2SDS

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 2,2,4-trimethylcyclohex-3-ene-1-carbaldehyde

1.2 Other means of identification

Product number -
Other names 3-Cyclohexene-1-carboxaldehyde,2,2,4-trimethyl

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:1726-47-2 SDS

1726-47-2Relevant academic research and scientific papers

A concise stereoselective synthesis of the C-aromatic taxane skeleton: An application of novel sequential transacetalation oxonium ene cyclization

Sonawane,Maji, Dilip K.,Jana,Pandey

, p. 1773 - 1774 (1998)

A three-step sequence for the construction of the C-aromatic taxane nucleus from easily available A-ring unit 2 and C-aromatic unit 3 is reported; SnCl4 promoted reaction of 4, presumably via the diastereoselective oxonium ene cyclisation react

Reductive opening of cyclopropylogous α-hydroxy aldehydes and ketones by samarium(II) iodide

Nivlet, Alex,Le Guen, Valerie,Dechoux, Luc,Le Gall, Thierry,Mioskowski, Charles

, p. 2115 - 2118 (1998)

The regioselectivity of the recluctive opening of cyclopropylogous α- hydroxy carbonyl compounds using SmI2 in THF or THF-HMPA was studied and shown to depend strongly on the substrate. In some cases, a tandem cyclopropyl opening-deoxygenation reaction afforded the corresponding γ- keto alkenes in one step.

β-Pinene-6-one: A pivotal synthetic intermediate

Hebrault,Uguen

, p. 6699 - 6702 (2007/10/03)

Submitting the title ketone to either acetoxymercuration or basic conditions resulted in the formation of the acid β-5 and α-5, respectively, with an useful selectivity, related rearrangements being observed by using the corresponding alcohol and its epoxy derivative.

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