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1,1'-(diphenylamine-2,2'-dicarbonyl)-bis[(2S)-α,α-diphenyl-2-pyrrolidinemethanol] is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

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  • 1164109-69-6 Structure
  • Basic information

    1. Product Name: 1,1'-(diphenylamine-2,2'-dicarbonyl)-bis[(2S)-α,α-diphenyl-2-pyrrolidinemethanol]
    2. Synonyms:
    3. CAS NO:1164109-69-6
    4. Molecular Formula:
    5. Molecular Weight: 727.903
    6. EINECS: N/A
    7. Product Categories: N/A
    8. Mol File: 1164109-69-6.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: 1,1'-(diphenylamine-2,2'-dicarbonyl)-bis[(2S)-α,α-diphenyl-2-pyrrolidinemethanol](CAS DataBase Reference)
    10. NIST Chemistry Reference: 1,1'-(diphenylamine-2,2'-dicarbonyl)-bis[(2S)-α,α-diphenyl-2-pyrrolidinemethanol](1164109-69-6)
    11. EPA Substance Registry System: 1,1'-(diphenylamine-2,2'-dicarbonyl)-bis[(2S)-α,α-diphenyl-2-pyrrolidinemethanol](1164109-69-6)
  • 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: 1164109-69-6(Hazardous Substances Data)

1164109-69-6 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 1164109-69-6 includes 10 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 7 digits, 1,1,6,4,1,0 and 9 respectively; the second part has 2 digits, 6 and 9 respectively.
Calculate Digit Verification of CAS Registry Number 1164109-69:
(9*1)+(8*1)+(7*6)+(6*4)+(5*1)+(4*0)+(3*9)+(2*6)+(1*9)=136
136 % 10 = 6
So 1164109-69-6 is a valid CAS Registry Number.

1164109-69-6Downstream Products

1164109-69-6Relevant articles and documents

Diphenylamine-derived bis-hydroxyamide catalyzed asymmetric borane reduction of prochiral ketones

Wang, Jin,Liu, Han,Du, Da-Ming

, p. 605 - 609 (2009)

A series of bis-hydroxyamides were synthesized from diphenylamine-2,2′-dicarboxylic acid and chiral aminoalcohols. Their catalytic activity in asymmetric borane reduction was investigated. After the fine optimization of solvents, temperature, amount of borane complex, and the length of catalyst generating period, good to excellent yields (55-99%) and enantioselectivities (79-97% ee) can be achieved in the reduction of aromatic and alkyl prochiral ketones. A transition state structure was proposed on the basis of absolute configuration and controlled experiment.

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