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1984862-45-4

N-[3,5-bis(trifluoroMethyl)phenyl-N'-[(1R,2R)-2-(11bS)3,5-dihydro-4H-dinaphth[2,1-c:1',2'-e]azepin-4-yl]cyclohexyl]-thiourea is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

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  • N-[3,5-bis(trifluoroMethyl)phenyl-N'-[(1R,2R)-2-(11bS)3,5-dihydro-4H-dinaphth[2,1-c:1',2'-e]azepin-4-yl]cyclohexyl]-thiourea

    Cas No: 1984862-45-4

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  • 1984862-45-4 Structure

  • Basic information

    1. Product Name: N-[3,5-bis(trifluoroMethyl)phenyl-N'-[(1R,2R)-2-(11bS)3,5-dihydro-4H-dinaphth[2,1-c:1',2'-e]azepin-4-yl]cyclohexyl]-thiourea
    2. Synonyms: N-[3,5-bis(trifluoroMethyl)phenyl-N'-[(1R,2R)-2-(11bS)3,5-dihydro-4H-dinaphth[2,1-c:1',2'-e]azepin-4-yl]cyclohexyl]-thiourea
    3. CAS NO:1984862-45-4
    4. Molecular Formula: C37H31F6N3S
    5. Molecular Weight: 663.72
    6. EINECS: N/A
    7. Product Categories: N/A
    8. Mol File: 1984862-45-4.mol

  • Chemical Properties

    1. Melting Point: N/A
    2. Boiling Point: N/A
    3. Flash Point: N/A
    4. Appearance: /
    5. Density: N/A
    6. Refractive Index: N/A
    7. Storage Temp.: N/A
    8. Solubility: N/A
    9. CAS DataBase Reference: N-[3,5-bis(trifluoroMethyl)phenyl-N'-[(1R,2R)-2-(11bS)3,5-dihydro-4H-dinaphth[2,1-c:1',2'-e]azepin-4-yl]cyclohexyl]-thiourea(CAS DataBase Reference)
    10. NIST Chemistry Reference: N-[3,5-bis(trifluoroMethyl)phenyl-N'-[(1R,2R)-2-(11bS)3,5-dihydro-4H-dinaphth[2,1-c:1',2'-e]azepin-4-yl]cyclohexyl]-thiourea(1984862-45-4)
    11. EPA Substance Registry System: N-[3,5-bis(trifluoroMethyl)phenyl-N'-[(1R,2R)-2-(11bS)3,5-dihydro-4H-dinaphth[2,1-c:1',2'-e]azepin-4-yl]cyclohexyl]-thiourea(1984862-45-4)

  • 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: 1984862-45-4(Hazardous Substances Data)

1984862-45-4 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 1984862-45-4 includes 10 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 7 digits, 1,9,8,4,8,6 and 2 respectively; the second part has 2 digits, 4 and 5 respectively.
Calculate Digit Verification of CAS Registry Number 1984862-45:
(9*1)+(8*9)+(7*8)+(6*4)+(5*8)+(4*6)+(3*2)+(2*4)+(1*5)=244
244 % 10 = 4
So 1984862-45-4 is a valid CAS Registry Number.

1984862-45-4Downstream Products

1984862-45-4Relevant articles and documents

Organocatalytic enantioselective Michael addition of malononitrile to nitroolefins catalyzed by bifunctional thiourea

Guo, Hai-Ming,Li, Jian-Guo,Qu, Gui-Rong,Zhang, Xiao-Mei,Yuan, Wei-Cheng

experimental part, p. 514 - 518 (2012/01/06)

A novel enantioselective Michael addition of malononitrile to trans-β-nitroolefins in the presence of bifunctional amine thiourea organocatalyst is developed. The Michael reaction catalyzed by amine thioureas containing both central and axial chiral eleme

Organocatalytic highly enantio- and diastereoselective Mannich reaction of β-ketoesters with N-boc-aldimines

Kang, Young Ku,Kim, Dae Young

supporting information; experimental part, p. 5734 - 5737 (2009/12/08)

(Figure Presented) The catalytic enantioselective Mannich reaction promoted by chiral bifunctional organocatalysts is described. The treatment of β-ketoesters with N-Boc-aldimines under mild reaction conditions afforded the corresponding β-amino β-ketoest

Enantio- and diastereoselective mannich-type reactions of α-Cyano ketones with N-Boc aldimines catalyzed by chiral bifunctional urea

Lee, Ju Hee,Kim, Dae Young

supporting information; experimental part, p. 1779 - 1782 (2011/02/26)

The catalytic enantioselective electrophilic Mannich-type reaction promoted by chiral bifunctional organocatalysts is described. The treatment of a-cyano ketones with N-Boc-aldimines under mild reaction conditions afforded the corresponding β-amino-α-cyan

Enantioselective direct amination of α-cyanoketones catalyzed by bifunctional organocatalysts

Kim, Sun Mi,Lee, Ju Hee,Kim, Dae Young

experimental part, p. 2659 - 2662 (2009/05/09)

The catalytic enantioselective electrophilic α-amination promoted by chiral bifunctional organocatalysts is described. Treatment of α-cyanoketones with azodicarboxylates as electrophilic animation reagents under mild reaction conditions afforded the corresponding a-aminated α-cyanoketones with excellent enantiomeric excesses (87-99%).

Catalytic enantioselective electrophilic α-hydrazination of β-ketoesters using bifunctional organocatalysts

Jung, Sun Hee,Kim, Dae Young

, p. 5527 - 5530 (2008/12/22)

The catalytic enantioselective electrophilic α-hydrazination promoted by chiral bifunctional organocatalysts is described. Treatment of β-ketoesters with azodicarboxylates as electrophilic amination reagents under mild reaction conditions afforded the cor

Organocatalytic enantioselective Michael addition of 2,4-pentandione to nitroalkenes promoted by bifunctional thioureas with central and axial chiral elements

Peng, Fang-Zhi,Shao, Zhi-Hui,Fan, Bao-Min,Song, He,Li, Gan-Peng,Zhang, Hong-Bin

, p. 5202 - 5205 (2008/09/21)

(Chemical Equation Presented) Two novel bifunctional amine-thiourea organocatalysts 1 and 2, which both bear central and axial chiral elements, have been developed to promote enantioselective Michael reaction between 1,3-dicarbonyl compounds and nitro ole

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