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CAS

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81390-19-4

methyl erythro-α,β-diphenylglycerate is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

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  • 81390-19-4 Structure

  • Basic information

    1. Product Name: methyl erythro-α,β-diphenylglycerate
    2. Synonyms:
    3. CAS NO:81390-19-4
    4. Molecular Formula:
    5. Molecular Weight: 272.301
    6. EINECS: N/A
    7. Product Categories: N/A
    8. Mol File: 81390-19-4.mol

  • Chemical Properties

    1. Melting Point: N/A
    2. Boiling Point: N/A
    3. Flash Point: N/A
    4. Appearance: N/A
    5. Density: N/A
    6. Refractive Index: N/A
    7. Storage Temp.: N/A
    8. Solubility: N/A
    9. CAS DataBase Reference: methyl erythro-α,β-diphenylglycerate(CAS DataBase Reference)
    10. NIST Chemistry Reference: methyl erythro-α,β-diphenylglycerate(81390-19-4)
    11. EPA Substance Registry System: methyl erythro-α,β-diphenylglycerate(81390-19-4)

  • 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: 81390-19-4(Hazardous Substances Data)

81390-19-4 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 81390-19-4 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 8,1,3,9 and 0 respectively; the second part has 2 digits, 1 and 9 respectively.
Calculate Digit Verification of CAS Registry Number 81390-19:
(7*8)+(6*1)+(5*3)+(4*9)+(3*0)+(2*1)+(1*9)=124
124 % 10 = 4
So 81390-19-4 is a valid CAS Registry Number.

81390-19-4Relevant articles and documents

Enantioselective equilibration-access to chiral aldol adducts of mandelic acid esters

Scholtis, Stefan,Ide, Andreas,Mahrwald, Rainer

, p. 5353 - 5355 (2007/10/03)

Syn-configured aldol products of mandelic acid esters and aldehydes were synthesized by the catalytic use of amines in the presence of titanium(IV) tert-butoxide. Used along with chiral N-methylephedrine, anti-configured α,β-dihydroxyesters were isolated

Efficient diastereoselective synthesis of α,β-dihydroxyesters from methyl phenylglyoxylate and aldehydes mediated by titanium trichloride/pyridine system

Clerici,Clerici,Malpezzi,Porta

, p. 13385 - 13400 (2007/10/02)

The reductive coupling of methyl phenylglyoxylate 2 with aliphatic and aromatic aldehydes 3, promoted by TiCl3/Py system in anhydrous THF, affords α,β-dihydroxyesters 4 in good yields (60-94%) and high syn-diastereoselectivity (up to 85%). The type of ligand at the metal ion necessary to achieve a high level of diastereocontrol and the possible mechanism involved are discussed.

A Novel Reaction Type Promoted by Aqueous Titanium Trichloride. Synthesis of Unsymmetrical 1,2-Diols

Clerici, Angelo,Porta, Ombretta

, p. 2852 - 2856 (2007/10/02)

Electron-withdrawing substituted carbonyl compounds when allowed to react with 2 equiv of aqueous titanium trichloride in the presence of acetone, acetaldehyde, or benzaldehyde afford unsymmetrical 1,2-diols in high yields under very simple experimental conditions.

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