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620164-01-4

Cyclohexanepropanoic acid, -ba--hydroxy--alpha--methyl-, methyl ester, (-alpha-S,-ba-S)- (9CI) is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

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  • 620164-01-4 Structure

  • Basic information

    1. Product Name: Cyclohexanepropanoic acid, -ba--hydroxy--alpha--methyl-, methyl ester, (-alpha-S,-ba-S)- (9CI)
    2. Synonyms: Cyclohexanepropanoicacid,-bta--hydroxy--alpha--methyl-,methylester,(-alpha-S,-bta-S)-(9CI);Cyclohexanepropanoic acid, -ba--hydroxy--alpha--methyl-, methyl ester, (-alpha-S,-ba-S)- (9CI);Cyclohexanepropanoic acid, -b
    3. CAS NO:620164-01-4
    4. Molecular Formula: C11H20O3
    5. Molecular Weight: 200.2747
    6. EINECS: N/A
    7. Product Categories: CYCLOHEXANE
    8. Mol File: 620164-01-4.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: Cyclohexanepropanoic acid, -ba--hydroxy--alpha--methyl-, methyl ester, (-alpha-S,-ba-S)- (9CI)(CAS DataBase Reference)
    10. NIST Chemistry Reference: Cyclohexanepropanoic acid, -ba--hydroxy--alpha--methyl-, methyl ester, (-alpha-S,-ba-S)- (9CI)(620164-01-4)
    11. EPA Substance Registry System: Cyclohexanepropanoic acid, -ba--hydroxy--alpha--methyl-, methyl ester, (-alpha-S,-ba-S)- (9CI)(620164-01-4)

  • 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: 620164-01-4(Hazardous Substances Data)

620164-01-4 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 620164-01-4 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 6,2,0,1,6 and 4 respectively; the second part has 2 digits, 0 and 1 respectively.
Calculate Digit Verification of CAS Registry Number 620164-01:
(8*6)+(7*2)+(6*0)+(5*1)+(4*6)+(3*4)+(2*0)+(1*1)=104
104 % 10 = 4
So 620164-01-4 is a valid CAS Registry Number.

620164-01-4Downstream Products

620164-01-4Relevant articles and documents

Copper-ClickFerrophos-complex-catalyzed enantioselective reductive aldol reaction

Kato, Minoru,Oki, Hiroshi,Ogata, Kenichi,Fukuzawa, Shin-Ichi

experimental part, p. 1299 - 1302 (2009/12/03)

We have prepared several ClickFerrophos families and tested for the Cu(I)-catalyzed asymmetric reductive aldol reaction of ketones and aldehydes with an acrylic ester in the presence of phenylsilane. The Cu(I)-ClickFerrophos complex is efficient for the r

Copper(I)-catalyzed enantio- and diastereoselective tandem reductive aldol reaction

Chuzel, Olivier,Deschamp, Julia,Chausteur, Christophe,Riant, Olivier

, p. 5943 - 5946 (2007/10/03)

(Chemical Equation Presented) An efficient method for the enantioselective tandem reductive aldol reaction of methyl acrylate with aldehydes is reported. By using a copper-(I) precursor and a proper diphosphane ligand, high reactivities can be reached, with TOF up to 40 000 h-1. Taniaphos-based ligands lead to enantioselectivities of up to 97% in the case of the major syn diastereoisomer.

DIRECT, ENANTIOSELECTIVE ALDOL COUPLING OF ALDEHYDES USING CHIRAL ORGANIC CATALYSTS

-

Page/Page column 22-23, (2008/06/13)

Nonmetallic, chiral organic catalysts are used to catalyze an enantioselective aldol coupling reaction between aldehyde substrates. The reaction may be carried out with a single enolizable aldehyde, resulting in dimerization to give a β-hydroxy aldehyde,

Synthesis of Optically Active (E)-1-Alkoxymethoxybut-2-enyl(tributyl)stannanes: Stereochemistry of their Thermal Reactions with Aldehydes

Jephcote, Vincent J.,Pratt, Andrew J.,Thomas, Eric J.

, p. 1529 - 1535 (2007/10/02)

(1R)- and (1S)-1--(E)-but-2-enyl(tributyl)stannanes (8) and (9), whose configurations were assigned by correlation with (2R)- and (2S)-pentan-2-ol (14) and (15), react stereoselectively on heating with benzaldehyde to give (3S,4S)- and (3R,4R)-4-hydroxy-3-methyl-(Z)-1,2-enol ethers (16) and (18), respectively, the configurations of these products being established by correlation with pseudoephedrine.

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