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CAS

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479544-01-9

Cyclohexanone, 3,5-diethyl-4,4-dimethoxy-, (3R,5R)- (9CI) is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

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  • 479544-01-9 Structure

  • Basic information

    1. Product Name: Cyclohexanone, 3,5-diethyl-4,4-dimethoxy-, (3R,5R)- (9CI)
    2. Synonyms: Cyclohexanone, 3,5-diethyl-4,4-dimethoxy-, (3R,5R)- (9CI)
    3. CAS NO:479544-01-9
    4. Molecular Formula: C12H22O3
    5. Molecular Weight: 214.30128
    6. EINECS: N/A
    7. Product Categories: ETHYL
    8. Mol File: 479544-01-9.mol

  • Chemical Properties

    1. Melting Point: N/A
    2. Boiling Point: N/A
    3. Flash Point: N/A
    4. Appearance: /
    5. Density: N/A
    6. Refractive Index: N/A
    7. Storage Temp.: N/A
    8. Solubility: N/A
    9. CAS DataBase Reference: Cyclohexanone, 3,5-diethyl-4,4-dimethoxy-, (3R,5R)- (9CI)(CAS DataBase Reference)
    10. NIST Chemistry Reference: Cyclohexanone, 3,5-diethyl-4,4-dimethoxy-, (3R,5R)- (9CI)(479544-01-9)
    11. EPA Substance Registry System: Cyclohexanone, 3,5-diethyl-4,4-dimethoxy-, (3R,5R)- (9CI)(479544-01-9)

  • 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: 479544-01-9(Hazardous Substances Data)

479544-01-9 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 479544-01-9 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 4,7,9,5,4 and 4 respectively; the second part has 2 digits, 0 and 1 respectively.
Calculate Digit Verification of CAS Registry Number 479544-01:
(8*4)+(7*7)+(6*9)+(5*5)+(4*4)+(3*4)+(2*0)+(1*1)=189
189 % 10 = 9
So 479544-01-9 is a valid CAS Registry Number.

479544-01-9SDS

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 (+)-trans-3,5-diethyl-4,4-dimethoxycyclohexanone

1.2 Other means of identification

Product number -
Other names (3R,5R)-3,5-Diethyl-4,4-dimethoxy-cyclohexanone

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:479544-01-9 SDS

479544-01-9Relevant articles and documents

A catalytic enantioselective route to cis- and trans-3,4,4,5-tetrasubstituted cyclohexanones; remarkable chiral catalyst control in sequential catalytic 1,4-additions to cyclohexadienones

Imbos, Rosalinde,Minnaard, Adriaan J,Feringa, Ben L

, p. 2485 - 2489 (2007/10/03)

Asymmetric copper-phosphoramidite catalysed conjugate addition of Et2Zn to easily accessible, nearly enantiomerically pure cyclohexenones 2 and 4 was performed. Depending on the enantiomer of the chiral phosphoramidite used, the cis- or trans-3,4,4,5-tetrasubstituted cyclohexanones 5 and 6 could be formed selectively. Surprisingly, there is no directing effect of the 5-ethyl- or 4-alkoxy-substituents and the stereochemical outcome is only governed by the configuration of the chiral ligand.

A catalytic route to acyclic chiral building blocks: Applications of the catalytic asymmetric conjugate addition of organozinc reagents to cyclic enones

Jagt, Richard B.C.,Imbos, Rosalinde,Naasz, Robert,Minnaard, Adriaan J.,Feringa, Ben L.

, p. 221 - 229 (2007/10/03)

Through the Cu-phosphoramidite-catalyzed asymmetric conjugate addition a number of chiral cyclic enones are available with high ee. Here we report the sequential conjugate addition to these enones as a route towards multisubstituted chiral cyclic ketones.

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