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CAS

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357675-06-0

methyl (R)-3-[(S)-2,2-dimethyl-1,3-dioxolan-4-yl]-3-phenylpropanoate is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

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  • 357675-06-0 Structure

  • Basic information

    1. Product Name: methyl (R)-3-[(S)-2,2-dimethyl-1,3-dioxolan-4-yl]-3-phenylpropanoate
    2. Synonyms: methyl (R)-3-[(S)-2,2-dimethyl-1,3-dioxolan-4-yl]-3-phenylpropanoate
    3. CAS NO:357675-06-0
    4. Molecular Formula:
    5. Molecular Weight: 264.321
    6. EINECS: N/A
    7. Product Categories: N/A
    8. Mol File: 357675-06-0.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 (R)-3-[(S)-2,2-dimethyl-1,3-dioxolan-4-yl]-3-phenylpropanoate(CAS DataBase Reference)
    10. NIST Chemistry Reference: methyl (R)-3-[(S)-2,2-dimethyl-1,3-dioxolan-4-yl]-3-phenylpropanoate(357675-06-0)
    11. EPA Substance Registry System: methyl (R)-3-[(S)-2,2-dimethyl-1,3-dioxolan-4-yl]-3-phenylpropanoate(357675-06-0)

  • 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: 357675-06-0(Hazardous Substances Data)

357675-06-0 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 357675-06-0 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 3,5,7,6,7 and 5 respectively; the second part has 2 digits, 0 and 6 respectively.
Calculate Digit Verification of CAS Registry Number 357675-06:
(8*3)+(7*5)+(6*7)+(5*6)+(4*7)+(3*5)+(2*0)+(1*6)=180
180 % 10 = 0
So 357675-06-0 is a valid CAS Registry Number.

357675-06-0Relevant articles and documents

Stereoselective conjugate addition of aryl- And alkenylboronic acids to acyclic γ,δ-oxygen-substituted α,β-enoates

Segura, Amaya,Csaky, Aurelio G.

, p. 3667 - 3670 (2007)

The substrate-controlled Rh1-catalyzed conjugate addition of aryl- and alkenylboronic acids to α,β-unsaturated esters which bear γ- and δ-oxygen substituents takes place in a highly anti diastereoselective fashion either when using γ-hydroxyl u

1,2-stereochemical induction in the PdII-catalyzed conjugate addition of boronic acids

Roscales, Silvia,Sánchez, Francisco,Csák?, Aurelio G.

, p. 1754 - 1763 (2015/05/27)

Palladium(II) catalysis has been used in the substrate-controlled 1,2-chiral induction of the conjugate addition of boronic acids to enantiopure α,β-unsaturated ketones and esters without competition from the Mirozoki-Heck reaction. Bedford's palladacycle

A study of conjugate addition to a γ,δ-dioxolanyl-α,β-unsaturated ester

Han, Guoxia,Hruby, Victor J.

, p. 4281 - 4283 (2007/10/03)

Diastereoselective phenylcuprate addition to (S)-3-(2,2-dimethyl-1,3-dioxolan-4-yl)-trans-2-propenoate has been achieved in the presence of lithium bromide, copper(I) cyanide, trimethylsilyl chloride and dimethylsulfide cocatalysts.

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