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(R)-2-(dimethylamino)-2-oxo-1-phenylethyl acetate is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

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  • 34469-08-4 Structure
  • Basic information

    1. Product Name: (R)-2-(dimethylamino)-2-oxo-1-phenylethyl acetate
    2. Synonyms:
    3. CAS NO:34469-08-4
    4. Molecular Formula:
    5. Molecular Weight: 221.256
    6. EINECS: N/A
    7. Product Categories: N/A
    8. Mol File: 34469-08-4.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: (R)-2-(dimethylamino)-2-oxo-1-phenylethyl acetate(CAS DataBase Reference)
    10. NIST Chemistry Reference: (R)-2-(dimethylamino)-2-oxo-1-phenylethyl acetate(34469-08-4)
    11. EPA Substance Registry System: (R)-2-(dimethylamino)-2-oxo-1-phenylethyl acetate(34469-08-4)
  • 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: 34469-08-4(Hazardous Substances Data)

34469-08-4 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 34469-08-4 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 3,4,4,6 and 9 respectively; the second part has 2 digits, 0 and 8 respectively.
Calculate Digit Verification of CAS Registry Number 34469-08:
(7*3)+(6*4)+(5*4)+(4*6)+(3*9)+(2*0)+(1*8)=124
124 % 10 = 4
So 34469-08-4 is a valid CAS Registry Number.

34469-08-4Relevant articles and documents

The Synthesis of Chiral α-Aryl α-Hydroxy Carboxylic Acids via RuPHOX-Ru Catalyzed Asymmetric Hydrogenation

Guo, Huan,Li, Jing,Liu, Delong,Zhang, Wanbin

, p. 3665 - 3673 (2017/09/11)

A ruthenocenyl phosphino-oxazoline-ruthenium complex (RuPHOX?Ru) catalyzed asymmetric hydrogenation of α-aryl keto acids has been successfully developed, affording the corresponding chiral α-aryl α-hydroxy carboxylic acids in high yields and with up to 97% ee. The reaction could be performed on a gram scale with a relatively low catalyst loading (up to 5000 S/C) and the resulting products can be transformed to several chiral building blocks, biologically active compounds and chiral drugs. (Figure presented.).

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