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1-Cyclohexene-1-carboxaldehyde, 2,6,6-trimethyl-3-oxo- is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

18378-66-0

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18378-66-0 Usage

Cyclic aldehyde

1-Cyclohexene-1-carboxaldehyde, 2,6,6-trimethyl-3-oxois a cyclic aldehyde, meaning it contains a carboxaldehyde functional group attached to a cyclohexene ring.

Cyclohexene ring

The compound contains a cyclohexene ring, which is a six-carbon ring with alternating single and double bonds.

Three methyl groups

The compound has three methyl groups attached to the carbon atoms in the cyclohexene ring, which contribute to its chemical and physical properties.

Used in fragrance and flavor industry

1-Cyclohexene-1-carboxaldehyde, 2,6,6-trimethyl-3-oxois commonly used in the fragrance and flavor industry as a component in perfumes, soaps, and other scented products.

Strong, sweet, floral odor

The compound has a strong, sweet, and floral odor, making it a popular choice for adding a pleasant and long-lasting scent to various products.

Check Digit Verification of cas no

The CAS Registry Mumber 18378-66-0 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 1,8,3,7 and 8 respectively; the second part has 2 digits, 6 and 6 respectively.
Calculate Digit Verification of CAS Registry Number 18378-66:
(7*1)+(6*8)+(5*3)+(4*7)+(3*8)+(2*6)+(1*6)=140
140 % 10 = 0
So 18378-66-0 is a valid CAS Registry Number.

18378-66-0SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 15, 2017

Revision Date: Aug 15, 2017

1.Identification

1.1 GHS Product identifier

Product name 4-oxo-β-cyclocitral

1.2 Other means of identification

Product number -
Other names 3-formyl-2,4,4-trimethyl-2-cyclohexen-1-one

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:18378-66-0 SDS

18378-66-0Relevant academic research and scientific papers

Practical Total Synthesis of (+/-)-Strigol

Brooks, Dee W.,Bevinakatti, H. S.,Kennedy, Eileen,Hathaway, Jim

, p. 628 - 632 (1985)

An improved total synthesis of racemic strigol (1) and 4'-epistrigol (21) from α-ionone in 10 (4.4percent overall yield) or 12 steps (6.8percent overall yield) by recycling isomer 16 is described which is applicable on a multigram scale with a minimum of

γ-Pyronene, a synthon derived from saffron and intermediary precursor of synthesis of forskolin and strigol

Boulin,Arreguy-San Miguel,Delmond

, p. 2753 - 2762 (2007/10/03)

γ-Pyronene, a terpenic synthon available from myrcene, is an excellent raw material for the preparation of numerous intermediates used in the synthesis of perfumes, retinoids and biological derivatives such as forskolin or strigol.

1-Formyl-tri- and tetramethyl-cyclohex-1-en-3-one oximes

-

, (2008/06/13)

1-Formyl-2,6,6-trimethyl-cyclohex-1-ene derivatives of the formula I STR1 where R is --H or --CH3 and A is O or NOH are prepared by nitrosylating the corresponding 1-formyl-2,6,6-trimethyl-cyclohex-1-ene or -cyclohex-2-ene and, where appropriate, hydrolyzing the resulting oxime (where A is NOH) to the corresponding ketone (where A is O). The compounds I, except where R is H and A is O, are novel.

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