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2-acetylamino-3-cyclohexyl-2,3-dideuteriopropanoic acid methyl ester is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

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  • 1018969-29-3 Structure
  • Basic information

    1. Product Name: 2-acetylamino-3-cyclohexyl-2,3-dideuteriopropanoic acid methyl ester
    2. Synonyms: 2-acetylamino-3-cyclohexyl-2,3-dideuteriopropanoic acid methyl ester
    3. CAS NO:1018969-29-3
    4. Molecular Formula:
    5. Molecular Weight: 229.288
    6. EINECS: N/A
    7. Product Categories: N/A
    8. Mol File: 1018969-29-3.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: 2-acetylamino-3-cyclohexyl-2,3-dideuteriopropanoic acid methyl ester(CAS DataBase Reference)
    10. NIST Chemistry Reference: 2-acetylamino-3-cyclohexyl-2,3-dideuteriopropanoic acid methyl ester(1018969-29-3)
    11. EPA Substance Registry System: 2-acetylamino-3-cyclohexyl-2,3-dideuteriopropanoic acid methyl ester(1018969-29-3)
  • 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: 1018969-29-3(Hazardous Substances Data)

1018969-29-3 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 1018969-29-3 includes 10 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 7 digits, 1,0,1,8,9,6 and 9 respectively; the second part has 2 digits, 2 and 9 respectively.
Calculate Digit Verification of CAS Registry Number 1018969-29:
(9*1)+(8*0)+(7*1)+(6*8)+(5*9)+(4*6)+(3*9)+(2*2)+(1*9)=173
173 % 10 = 3
So 1018969-29-3 is a valid CAS Registry Number.

1018969-29-3Upstream product

1018969-29-3Downstream Products

1018969-29-3Relevant articles and documents

Synthesis and synthetic applications of α,β-dideuterio-α- amino esters promoted by samarium diiodide

Concellón, José M.,Rodríguez-Solla, Humberto,Concellón, Carmen,Tuya, Paula

, p. 402 - 404 (2008)

A new, easy, and high-yielded route to isotopically labeled amino acid derivatives is reported. This process takes place through a SmI 2-promoted 1,4-reduction of a variety of dehydroamino esters in the presence of D2O. The dideuteri

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