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4-(diethoxymethyl)cyclohexene is an organic compound with the molecular formula C11H22O2. It is a colorless liquid that is insoluble in water but soluble in organic solvents. This chemical is characterized by a cyclohexene ring with a diethoxymethyl group attached at the 4-position. The diethoxymethyl group consists of a central carbon atom bonded to three hydrogen atoms and two ethoxy groups, which are ethyl groups with an oxygen atom attached. 4-(diethoxymethyl)cyclohexene is used as an intermediate in the synthesis of various pharmaceuticals and agrochemicals, particularly in the production of certain pesticides and fragrances. Its chemical structure and reactivity make it a valuable building block in organic chemistry, allowing for further functionalization and the creation of more complex molecules.

6314-88-1

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6314-88-1 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 6314-88-1 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 6,3,1 and 4 respectively; the second part has 2 digits, 8 and 8 respectively.
Calculate Digit Verification of CAS Registry Number 6314-88:
(6*6)+(5*3)+(4*1)+(3*4)+(2*8)+(1*8)=91
91 % 10 = 1
So 6314-88-1 is a valid CAS Registry Number.

6314-88-1SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 13, 2017

Revision Date: Aug 13, 2017

1.Identification

1.1 GHS Product identifier

Product name 4-(diethoxymethyl)cyclohexene

1.2 Other means of identification

Product number -
Other names Cyclohex-3-encarbaldehyd-diaethylacetal

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:6314-88-1 SDS

6314-88-1Relevant academic research and scientific papers

A (3 - alkoxy - 4 - hydroxy) - cyclohexyl acetal glycol and its isomers of use

-

Paragraph 0054-0055, (2017/08/26)

The present invention discloses a (3-alkoxy-4-hydroxy)-cyclohexyl methylal diol, an (3-hydroxy-4-alkoxy)-cyclohexyl methylal diol and synthesis methods and use therefor. The (3-alkoxy-4-hydroxy)-cyclohexyl methylal diol and (3-hydroxy-4-alkoxy)-cyclohexyl methylal diol can be used for synthesis of a variety of vanillin and iso-vanillin. Compared to the existing synthetic method, the synthesis method has simple steps, and less discharge of "three wastes".

A 3, 4 - epoxy-cyclohexane METHYLAL glycol and its synthesis and use

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Paragraph 0055; 0056, (2017/11/16)

The invention discloses a 3,4-epoxy cyclohexyl methylal diol and a synthesis method thereof. The 3,4-epoxy cyclohexyl methylal diol can be used for synthesizing multiple vanillins and isovanillins. Compared with the existing synthesis process, the synthesis method disclosed by the invention has the advantages of simple steps and low discharge amount of three wastes.

Cyclohexane Diester Analogues of Phorbol Ester as Potential Activators of Protein Kinase C

Kerr, David E.,Kissinger, Lon F.,Shoyab, Mohammed

, p. 1958 - 1962 (2007/10/02)

Phospholipid-dependent, Ca2+-sensitive protein kinase (protein kinase C) is activated by the plant product phorbol ester at nanomolar concentrations and also in vivo at micromolar concentrations by diacylglycerols.We designed and synthesized cy

CHEMISTRY OF ENOL ETHERS. LIII. PROTOTROPIC ISOMERIZATION IN THE SERIES OF CYCLIC 1-ALKOXY-1,4-DIENES

Makin, S. M.,Pomogaev, A. I.,Boiko, T. N.,Nikiforova, A. P.

, p. 2033 - 2036 (2007/10/02)

A series of diethyl acetals of 1-cyclohexene-3-carbaldehydes, the pyrolysis of which leads to the formation of cyclic 1-ethoxy-1,4-dienes, were obtained by the acetalization of 1-cyclohexene-3-carbaldehydes, which were obtained by the condensation of conjugated dienes with α,β-unsaturated aldehydes.The prototropic isomerization of the 1-ethoxy-1,4-dienes to corresponding 1-ethoxy-1,3-dienes under the influence of potassium tert-butoxide in dimethyl sulfoxide solution was investigated.

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