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CAS

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1403666-74-9

2-(3-bromopropyl)-N,N-dimethyl-4,4-diphenyl-4H-benzo[d][1,3]dioxin-6-amine is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

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  • 1403666-74-9 Structure

  • Basic information

    1. Product Name: 2-(3-bromopropyl)-N,N-dimethyl-4,4-diphenyl-4H-benzo[d][1,3]dioxin-6-amine
    2. Synonyms: 2-(3-bromopropyl)-N,N-dimethyl-4,4-diphenyl-4H-benzo[d][1,3]dioxin-6-amine
    3. CAS NO:1403666-74-9
    4. Molecular Formula:
    5. Molecular Weight: 452.391
    6. EINECS: N/A
    7. Product Categories: N/A
    8. Mol File: 1403666-74-9.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: 2-(3-bromopropyl)-N,N-dimethyl-4,4-diphenyl-4H-benzo[d][1,3]dioxin-6-amine(CAS DataBase Reference)
    10. NIST Chemistry Reference: 2-(3-bromopropyl)-N,N-dimethyl-4,4-diphenyl-4H-benzo[d][1,3]dioxin-6-amine(1403666-74-9)
    11. EPA Substance Registry System: 2-(3-bromopropyl)-N,N-dimethyl-4,4-diphenyl-4H-benzo[d][1,3]dioxin-6-amine(1403666-74-9)

  • 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: 1403666-74-9(Hazardous Substances Data)

1403666-74-9 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 1403666-74-9 includes 10 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 7 digits, 1,4,0,3,6,6 and 6 respectively; the second part has 2 digits, 7 and 4 respectively.
Calculate Digit Verification of CAS Registry Number 1403666-74:
(9*1)+(8*4)+(7*0)+(6*3)+(5*6)+(4*6)+(3*6)+(2*7)+(1*4)=149
149 % 10 = 9
So 1403666-74-9 is a valid CAS Registry Number.

1403666-74-9Relevant articles and documents

A photocleavable linker for the chemoselective functionalization of biomaterials

O'Donovan, Liz,De Bank, Paul A.

, p. 21878 - 21884,7 (2012)

The functionalization of matrices with "caged" functional groups and their subsequent selective uncaging is a promising approach for generating patterns of bioactive molecules to guide cell growth or recreate in vivo microarchitectures. To date, this has been limited to caged carboxylic acids, amines and thiols, functional groups found within biological systems. We present a bifunctional caged carbonyl linker as an alternative approach for the chemoselective functionalization of biomaterials. This linker was readily coupled to collagen, employed as a model biomaterial, and underwent rapid uncaging in aqueous media upon irradiation with ultraviolet light to yield free carbonyl groups. Modified surfaces proved to be non-adhesive to cells until the chemoselective reintroduction of adhesion following incubation of uncaged carbonyls with gelatin hydrazide, with native gelatin failing to elicit a cellular response.

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