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CAS

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108896-77-1

N-(3-CHLOROBENZYL)-N-(2-[(3-CHLOROBENZYL)AMINO]ETHYL)AMINE is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

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  • 108896-77-1 Structure

  • Basic information

    1. Product Name: N-(3-CHLOROBENZYL)-N-(2-[(3-CHLOROBENZYL)AMINO]ETHYL)AMINE
    2. Synonyms: N-(3-CHLOROBENZYL)-N-(2-[(3-CHLOROBENZYL)AMINO]ETHYL)AMINE;N1,N2-BIS(3-CHLOROBENZYL)-1,2-ETHANEDIAMINE
    3. CAS NO:108896-77-1
    4. Molecular Formula: C16H18Cl2N2
    5. Molecular Weight: 309.23
    6. EINECS: N/A
    7. Product Categories: N/A
    8. Mol File: 108896-77-1.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-CHLOROBENZYL)-N-(2-[(3-CHLOROBENZYL)AMINO]ETHYL)AMINE(CAS DataBase Reference)
    10. NIST Chemistry Reference: N-(3-CHLOROBENZYL)-N-(2-[(3-CHLOROBENZYL)AMINO]ETHYL)AMINE(108896-77-1)
    11. EPA Substance Registry System: N-(3-CHLOROBENZYL)-N-(2-[(3-CHLOROBENZYL)AMINO]ETHYL)AMINE(108896-77-1)

  • 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: 108896-77-1(Hazardous Substances Data)

108896-77-1 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 108896-77-1 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,0,8,8,9 and 6 respectively; the second part has 2 digits, 7 and 7 respectively.
Calculate Digit Verification of CAS Registry Number 108896-77:
(8*1)+(7*0)+(6*8)+(5*8)+(4*9)+(3*6)+(2*7)+(1*7)=171
171 % 10 = 1
So 108896-77-1 is a valid CAS Registry Number.

108896-77-1Relevant articles and documents

Synthesis and biological evaluation of novel substituted-imidazolidine derivatives

Husain, Asif,Bhutani, Rubina,Kumar, Deepak,Shin, Dong-Soo

, p. 227 - 233 (2013/07/26)

A series of newer substituted-imidazolidine derivatives 3a-k were synthesized and assayed in vivo to investigate their anti-inflammatory, analgesic and antiulcer activity. The results of biological evaluation revealed that the three compounds, 4-[1,3-bis(4-hydroxy-3-methoxybenzyl)-2- imidazolidinyl]phenyldiethylamine (3g), 4-[1,3-bis(3-Ethoxy-4-hydroxybenzyl)-2- imidazolidinyl] phenyldiethylamine (3h) and 4-(1,3-bis(benzo[d][1,3]dioxol-5- ylmethyl)-4-methylimidazolidin-2-yl)-N,N-diethylbenzenamine (3j) were good in their anti-inflammatory and analgesic actions. Additionally these derivatives showed superior GI safety profile as compared to that of the standard drug in terms of low severity index. The results are statistically treated for its significance.

Novel inhibitors for multidrug resistance: 1,3,5-Triazacycloheptanes

Sawanishi,Wakusawa,Murakami,Muramatsu,Suzuki,Takashima,Aizawa,Miyamoto

, p. 5066 - 5070 (2007/10/03)

1,3,5-Triazacycloheptanes were synthesized and examined for reversal of the multidrug resistance dependent on P-glycoprotein. Most of these compounds increased the intracellular uptake of vinblastine in multidrug-resistant mouse leukemia P388/ADR cells wi

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