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N-[(1R,2R)-2-[[[[(1R,2R)-2-(diMethylaMino)cyclohexyl]aMino]thioxoMethyl]aMino]-1,2-diphenylethyl]-3,5-bis(trifluoroMethyl)-BenzenesulfonaMide is a chiral bifunctional organocatalyst with a complex molecular structure. It is characterized by its unique arrangement of atoms and functional groups, which allows it to selectively catalyze asymmetric reactions in organic synthesis.

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  • 3-[(1R,2R)-2-[3,5-bis(trifluoromethyl)benzenesulfonamido]-1,2-diphenylethyl]-1-[(1R,2R)-2-(dimethylamino)cyclohexyl]thiourea

    Cas No: 1020665-73-9

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  • N-[(1R,2R)-2-[[[[(1R,2R)-2-(diMethylaMino)cyclohexyl]aMino]thioxoMethyl]aMino]-1,2-diphenylethyl]-3,5-bis(trifluoroMethyl)-BenzenesulfonaMide

    Cas No: 1020665-73-9

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  • N-?[(1R,?2R)?-?2-?[[[[(1R,?2R)?-?2-?(Dimethylamino)?cyclohexyl]?amino]?thioxomethyl]?amino]?-?1,?2-?diphenylethyl]?-?3,?5-?bis(trifluoromethyl)?benzenesulfonamide

    Cas No: 1020665-73-9

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  • 1020665-73-9 Structure
  • Basic information

    1. Product Name: N-[(1R,2R)-2-[[[[(1R,2R)-2-(diMethylaMino)cyclohexyl]aMino]thioxoMethyl]aMino]-1,2-diphenylethyl]-3,5-bis(trifluoroMethyl)-BenzenesulfonaMide
    2. Synonyms: N-[(1R,2R)-2-[[[[(1R,2R)-2-(diMethylaMino)cyclohexyl]aMino]thioxoMethyl]aMino]-1,2-diphenylethyl]-3,5-bis(trifluoroMethyl)-BenzenesulfonaMide;N-((1R,2R)-2-(3-((1R,2R)-2-(Dimethylamino)cyclohexyl)thioureido)-1,2-diphenylethyl)-3,5-bis(trifluoromethyl)benzenesulfonamide;N-[(1R,2R)-2-[[[[(1R,2R)-2-(Dimethylamino)cyclohexyl]amino]thioxomethyl]amino]-1,2-diphenylethyl]-3,5-bis(trifluoromethyl)benzenesulfonamide,99%e.e.
    3. CAS NO:1020665-73-9
    4. Molecular Formula: C31H34F6N4O2S2
    5. Molecular Weight: 672.7476792
    6. EINECS: N/A
    7. Product Categories: N/A
    8. Mol File: 1020665-73-9.mol
  • Chemical Properties

    1. Melting Point: 168-170 °C
    2. Boiling Point: 677.5±65.0 °C(Predicted)
    3. Flash Point: N/A
    4. Appearance: /
    5. Density: 1.38±0.1 g/cm3(Predicted)
    6. Refractive Index: N/A
    7. Storage Temp.: under inert gas (nitrogen or Argon) at 2-8°C
    8. Solubility: N/A
    9. PKA: 8.51±0.50(Predicted)
    10. CAS DataBase Reference: N-[(1R,2R)-2-[[[[(1R,2R)-2-(diMethylaMino)cyclohexyl]aMino]thioxoMethyl]aMino]-1,2-diphenylethyl]-3,5-bis(trifluoroMethyl)-BenzenesulfonaMide(CAS DataBase Reference)
    11. NIST Chemistry Reference: N-[(1R,2R)-2-[[[[(1R,2R)-2-(diMethylaMino)cyclohexyl]aMino]thioxoMethyl]aMino]-1,2-diphenylethyl]-3,5-bis(trifluoroMethyl)-BenzenesulfonaMide(1020665-73-9)
    12. EPA Substance Registry System: N-[(1R,2R)-2-[[[[(1R,2R)-2-(diMethylaMino)cyclohexyl]aMino]thioxoMethyl]aMino]-1,2-diphenylethyl]-3,5-bis(trifluoroMethyl)-BenzenesulfonaMide(1020665-73-9)
  • 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: 1020665-73-9(Hazardous Substances Data)

1020665-73-9 Usage

Uses

Used in Pharmaceutical Industry:
N-[(1R,2R)-2-[[[[(1R,2R)-2-(diMethylaMino)cyclohexyl]aMino]thioxoMethyl]aMino]-1,2-diphenylethyl]-3,5-bis(trifluoroMethyl)-BenzenesulfonaMide is used as a chiral bifunctional organocatalyst for asymmetric synthesis in the pharmaceutical industry. It enables the production of enantiomerically pure compounds, which are essential for the development of new drugs with improved efficacy and reduced side effects.
Used in Chemical Industry:
In the chemical industry, N-[(1R,2R)-2-[[[[(1R,2R)-2-(diMethylaMino)cyclohexyl]aMino]thioxoMethyl]aMino]-1,2-diphenylethyl]-3,5-bis(trifluoroMethyl)-BenzenesulfonaMide is used as a chiral bifunctional organocatalyst for the synthesis of chiral compounds with specific properties. These compounds are valuable in various applications, such as agrochemicals, fragrances, and specialty chemicals.
Used in Research and Development:
N-[(1R,2R)-2-[[[[(1R,2R)-2-(diMethylaMino)cyclohexyl]aMino]thioxoMethyl]aMino]-1,2-diphenylethyl]-3,5-bis(trifluoroMethyl)-BenzenesulfonaMide is also used in research and development for the discovery and optimization of new asymmetric synthetic methods. Its unique properties and reactivity make it a valuable tool for exploring new reaction pathways and developing more efficient and selective catalytic processes.

Check Digit Verification of cas no

The CAS Registry Mumber 1020665-73-9 includes 10 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 7 digits, 1,0,2,0,6,6 and 5 respectively; the second part has 2 digits, 7 and 3 respectively.
Calculate Digit Verification of CAS Registry Number 1020665-73:
(9*1)+(8*0)+(7*2)+(6*0)+(5*6)+(4*6)+(3*5)+(2*7)+(1*3)=109
109 % 10 = 9
So 1020665-73-9 is a valid CAS Registry Number.

1020665-73-9SDS

SAFETY DATA SHEETS

According to Globally Harmonized System of Classification and Labelling of Chemicals (GHS) - Sixth revised edition

Version: 1.0

Creation Date: Aug 20, 2017

Revision Date: Aug 20, 2017

1.Identification

1.1 GHS Product identifier

Product name 1-[(1R,2R)-2-[[3,5-bis(trifluoromethyl)phenyl]sulfonylamino]-1,2-diphenylethyl]-3-[(1R,2R)-2-(dimethylamino)cyclohexyl]thiourea

1.2 Other means of identification

Product number -
Other names N-((1R,2R)-2-(3-((1R,2R)-2-(Dimethylamino)cyclohexyl)thioureido)-1,2-diphenylethyl)-3,5-bis(trifluoromethyl)benzenesulfonamide

1.3 Recommended use of the chemical and restrictions on use

Identified uses For industry use only.
Uses advised against no data available

1.4 Supplier's details

1.5 Emergency phone number

Emergency phone number -
Service hours Monday to Friday, 9am-5pm (Standard time zone: UTC/GMT +8 hours).

More Details:1020665-73-9 SDS

1020665-73-9Downstream Products

1020665-73-9Relevant articles and documents

Chiral amine-thioureas bearing multiple hydrogen bonding donors: Highly efficient organocatalysts for asymmetric Michael addition of acetylacetone to nitroolefins

Wang, Chun-Jiang,Zhang, Zhi-Hai,Dong, Xiu-Qin,Wu, Xiao-Jun

, p. 1431 - 1433 (2008/12/21)

New bifunctional organocatalysts amine-thioureas bearing multiple hydrogen bonding donors were synthesized and applied in catalytic asymmetric Michael addition of acetylacetone to aryl and alkyl nitroolefins. Multiple hydrogen bonding donors play a signif

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