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943901-45-9

(+)-(R)-dimethyl {1-[(trityloxy)methyl]prop-2-en-1-yl}malonate is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

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  • 943901-45-9 Structure

  • Basic information

    1. Product Name: (+)-(R)-dimethyl {1-[(trityloxy)methyl]prop-2-en-1-yl}malonate
    2. Synonyms: (+)-(R)-dimethyl {1-[(trityloxy)methyl]prop-2-en-1-yl}malonate
    3. CAS NO:943901-45-9
    4. Molecular Formula:
    5. Molecular Weight: 444.527
    6. EINECS: N/A
    7. Product Categories: N/A
    8. Mol File: 943901-45-9.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: (+)-(R)-dimethyl {1-[(trityloxy)methyl]prop-2-en-1-yl}malonate(CAS DataBase Reference)
    10. NIST Chemistry Reference: (+)-(R)-dimethyl {1-[(trityloxy)methyl]prop-2-en-1-yl}malonate(943901-45-9)
    11. EPA Substance Registry System: (+)-(R)-dimethyl {1-[(trityloxy)methyl]prop-2-en-1-yl}malonate(943901-45-9)

  • 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: 943901-45-9(Hazardous Substances Data)

943901-45-9 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 943901-45-9 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 9,4,3,9,0 and 1 respectively; the second part has 2 digits, 4 and 5 respectively.
Calculate Digit Verification of CAS Registry Number 943901-45:
(8*9)+(7*4)+(6*3)+(5*9)+(4*0)+(3*1)+(2*4)+(1*5)=179
179 % 10 = 9
So 943901-45-9 is a valid CAS Registry Number.

943901-45-9Relevant articles and documents

Highly regioselective allylic substitution reactions catalyzed by an air-stable (π-Allyl)iridium complex derived from dinaphthocyclooctatetraene and a phosphoramidite ligand

Ye, Ke-Yin,Zhao, Zhuo-An,Lai, Zeng-Wei,Dai, Li-Xin,You, Shu-Li

, p. 2109 - 2114 (2013/08/23)

An air-stable (π-allyl)iridium complex derived from dinaphthocyclooctatetraene and a phosphoramidite ligand has been synthesized and found to be highly efficient in iridium-catalyzed allylic substitution reactions. This catalyst features excellent regiose

Iridium-catalyzed allylic substitutions with cyclometalated phosphoramidite complexes bearing a dibenzocyclooctatetraene ligand: Preparation of (π-Allyl)Ir complexes and computational and NMR spectroscopic studies

Raskatov, Jevgenij A.,Jaekel, Mascha,Straub, Bernd F.,Rominger, Frank,Helmchen, Guenter

, p. 14314 - 14328 (2013/01/15)

(π-Allyl)Ir complexes derived from dibenzocyclooctatetraene and phosphoramidites by cyclometalation are effective catalysts for allylic substitution reactions of linear monosubstituted allylic carbonates. These catalysts provide exceptionally high degrees

Enantioselective Iridium-catalyzed allylic alkylations - Improvements and applications based on salt-free reaction conditions

Gnamm, Christian,F?rster, Sebastian,Miller, Nicole,Br?dner, Kerstin,Helmchen, Günter

, p. 790 - 794 (2007/12/29)

Simplified procedures for the Ir-catalyzed asymmetric allylic alkylation reaction are described that often allow substitution products to be obtained with ≥99% ee. Applications to syntheses of important chiral building blocks, such as the Taniguchi lacton

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