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CAS

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7494-85-1

2,2-dimethoxycyclohexyl acetate is a chemical compound with the molecular formula C10H18O4. It is a colorless liquid that is soluble in organic solvents and has a fruity, floral odor. 2,2-dimethoxycyclohexyl acetate is primarily used as a fragrance ingredient in various personal care products, such as perfumes, soaps, and lotions, due to its pleasant scent. It is also employed as a flavoring agent in food and beverages, imparting a fruity taste. The compound is synthesized through the esterification of 2,2-dimethoxycyclohexanol with acetic acid, and it is considered to be relatively stable and non-toxic. However, like many chemicals, it should be handled with care and used in accordance with safety guidelines to minimize potential health risks.

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  • 7494-85-1 Structure

  • Basic information

    1. Product Name: 2,2-dimethoxycyclohexyl acetate
    2. Synonyms:
    3. CAS NO:7494-85-1
    4. Molecular Formula: C10H18O4
    5. Molecular Weight: 202.2475
    6. EINECS: N/A
    7. Product Categories: N/A
    8. Mol File: 7494-85-1.mol

  • Chemical Properties

    1. Melting Point: N/A
    2. Boiling Point: 236.3°C at 760 mmHg
    3. Flash Point: 94.5°C
    4. Appearance: N/A
    5. Density: 1.05g/cm3
    6. Vapor Pressure: 0.0479mmHg at 25°C
    7. Refractive Index: 1.449
    8. Storage Temp.: N/A
    9. Solubility: N/A
    10. CAS DataBase Reference: 2,2-dimethoxycyclohexyl acetate(CAS DataBase Reference)
    11. NIST Chemistry Reference: 2,2-dimethoxycyclohexyl acetate(7494-85-1)
    12. EPA Substance Registry System: 2,2-dimethoxycyclohexyl acetate(7494-85-1)

  • Safety Data

    1. Hazard Codes: N/A
    2. Statements: N/A
    3. Safety Statements: N/A
    4. WGK Germany:
    5. RTECS:
    6. HazardClass: N/A
    7. PackingGroup: N/A
    8. Hazardous Substances Data: 7494-85-1(Hazardous Substances Data)

7494-85-1 Usage

Physical state

Colorless, oily liquid

Odor

Pleasant, fruity

Common uses

Fragrance ingredient in cosmetics and personal care products, solvent in inks, coatings, and adhesives

Industrial applications

Pharmaceuticals, agrochemicals

Notable properties

Low volatility, low odor, excellent solvency

Safety precautions

Can be harmful if ingested or if it comes into contact with the skin or eyes

Check Digit Verification of cas no

The CAS Registry Mumber 7494-85-1 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 7,4,9 and 4 respectively; the second part has 2 digits, 8 and 5 respectively.
Calculate Digit Verification of CAS Registry Number 7494-85:
(6*7)+(5*4)+(4*9)+(3*4)+(2*8)+(1*5)=131
131 % 10 = 1
So 7494-85-1 is a valid CAS Registry Number.

7494-85-1SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 16, 2017

Revision Date: Aug 16, 2017

1.Identification

1.1 GHS Product identifier

Product name (2,2-dimethoxycyclohexyl) acetate

1.2 Other means of identification

Product number -
Other names -

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:7494-85-1 SDS

7494-85-1Relevant articles and documents

Ring-Chain Tautomerism Provides a Route to 7a-Hydroxy-3a-methyl-2,7-dioxoperhydrobenzofuran. Synthesis of the Hydroxy γ-Lactone Substructure of Myrocin and Other Bioactive Natural Products

Langschwager, Wolf,Hoffmann, H. Martin R.

, p. 797 - 802 (2007/10/02)

(2-Oxocyclohexyl)acetic acid 10 was converted into bicyclic alkoxy γ-lactones 12a-d via intermediate chloro lactone 11 and alkanolysis.Similarly, lactones 15a,b and 18 were prepared.In contrast, simple ring-chain tautomerism directly afforded the title heterocycle 28, a crystalline, stable and welldefined compound.The angular methyl group seems essential for the spontaneous lactonization. 5,5-Dialkoxy-4-oxocarboxylic acids 26a, b without an angular methyl group did not cyclize to bicyclic hydroxy γ-lactones. - Key Words: Hydroxy lactone, 5-membered, (lactol) tautomer / 4-Oxocarboxylic acids / Keto-cyclol tautomerism.

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