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1012369-67-3

(R)-tert-butyl 2-cyclohexyl-5-oxopyrrolidine-1-carboxylate is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

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  • 1012369-67-3 Structure

  • Basic information

    1. Product Name: (R)-tert-butyl 2-cyclohexyl-5-oxopyrrolidine-1-carboxylate
    2. Synonyms: (R)-tert-butyl 2-cyclohexyl-5-oxopyrrolidine-1-carboxylate
    3. CAS NO:1012369-67-3
    4. Molecular Formula:
    5. Molecular Weight: 267.368
    6. EINECS: N/A
    7. Product Categories: N/A
    8. Mol File: 1012369-67-3.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: (R)-tert-butyl 2-cyclohexyl-5-oxopyrrolidine-1-carboxylate(CAS DataBase Reference)
    10. NIST Chemistry Reference: (R)-tert-butyl 2-cyclohexyl-5-oxopyrrolidine-1-carboxylate(1012369-67-3)
    11. EPA Substance Registry System: (R)-tert-butyl 2-cyclohexyl-5-oxopyrrolidine-1-carboxylate(1012369-67-3)

  • 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: 1012369-67-3(Hazardous Substances Data)

1012369-67-3 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 1012369-67-3 includes 10 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 7 digits, 1,0,1,2,3,6 and 9 respectively; the second part has 2 digits, 6 and 7 respectively.
Calculate Digit Verification of CAS Registry Number 1012369-67:
(9*1)+(8*0)+(7*1)+(6*2)+(5*3)+(4*6)+(3*9)+(2*6)+(1*7)=113
113 % 10 = 3
So 1012369-67-3 is a valid CAS Registry Number.

1012369-67-3Relevant articles and documents

N-heterocyclic carbene and Bronsted acid cooperative catalysis: Asymmetric synthesis of trans -γ-Lactams

Zhao, Xiaodan,Dirocco, Daniel A.,Rovis, Tomislav

, p. 12466 - 12469 (2011/09/16)

An efficient enantioselective approach to form trans-γ-lactams in up to 99% yield, 93% ee, and >20/1 dr using unactivated imines has been developed. The cyclohexyl-substituted azolium and the weak base sodium o-chlorobenzoate are most suitable for this tr

Highly diastereoselective addition of the lithium enolate of α-diazoacetoacetate to N-sulfinyl imines: Enantioselective synthesis of 2-oxo and 3-oxo pyrrolidines

Dong, Changqing,Mo, Fanyang,Wang, Jianbo

, p. 1971 - 1974 (2008/09/18)

(Chemical Equation Presented) The highly enantioselective synthesis of 2-oxo and 3-oxo pyrrolidines has been achieved by diastereoselective addition of the lithium enolate of α-diazoacetoacetate to chiral N-sulfinyl imines, followed by photoinduced Wolff rearrangement or Rh(II)-catalyzed intramolecular N-H insertion.

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