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N-cyclohexyl-2-benzoselenophenemethaneamine is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

84322-06-5

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  • 84322-06-5 Structure

  • Basic information

    1. Product Name: N-cyclohexyl-2-benzoselenophenemethaneamine
    2. Synonyms: N-cyclohexyl-2-benzoselenophenemethaneamine
    3. CAS NO:84322-06-5
    4. Molecular Formula:
    5. Molecular Weight: 292.283
    6. EINECS: N/A
    7. Product Categories: N/A

  • 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: N-cyclohexyl-2-benzoselenophenemethaneamine(CAS DataBase Reference)
    10. NIST Chemistry Reference: N-cyclohexyl-2-benzoselenophenemethaneamine(84322-06-5)
    11. EPA Substance Registry System: N-cyclohexyl-2-benzoselenophenemethaneamine(84322-06-5)

  • 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: 84322-06-5(Hazardous Substances Data)

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84322-06-5 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 84322-06-5 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 8,4,3,2 and 2 respectively; the second part has 2 digits, 0 and 6 respectively.
Calculate Digit Verification of CAS Registry Number 84322-06:
(7*8)+(6*4)+(5*3)+(4*2)+(3*2)+(2*0)+(1*6)=115
115 % 10 = 5
So 84322-06-5 is a valid CAS Registry Number.

84322-06-5Downstream Products

84322-06-5Relevant academic research and scientific papers

Amide-Amine Replacement in Indole-2-carboxamides Yields Potent Mycobactericidal Agents with Improved Water Solubility

Tan, Yu Jia,Li, Ming,Gunawan, Gregory Adrian,Nyantakyi, Samuel Agyei,Dick, Thomas,Go, Mei-Lin,Lam, Yulin

supporting information, p. 704 - 712 (2020/11/30)

Indolecarboxamides are potent but poorly soluble mycobactericidal agents. Here we found that modifying the incipient scaffold by amide-amine substitution and replacing the indole ring with benzothiophene or benzoselenophene led to striking (10-20-fold) im

SYNTHESIS AND STUDY OF THE LIGHT-STABILIZING ACTIVITY OF SOME DITHIOCARBAMATES THAT INCLUDE A HETEROAROMATIC RING

Gol'dfarb, Ya. L.,Ostapenko, E'. G.,Ivanov, V.B.,Efremkin, A. F.,Litvinov, V. P.

, p. 1148 - 1153 (2007/10/02)

A number of new dithiocarbamates of transition metals that contain thiophene, furan, benzothiophene, and benzoselenophene rings were synthesized.The compounds obtained were investigated as light stabilizers for polymers.It is shown that the effectiv

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