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2,1,3-Benzoxadiazol-4-amine, N-[7-[[2,3-bis[4-(1-ethoxyethoxy)phenyl]pentyl]thio]heptyl]-7-nitro- is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

104947-13-9

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  • 2,1,3-Benzoxadiazol-4-amine, N-[7-[[2,3-bis[4-(1-ethoxyethoxy)phenyl]pentyl]thio]heptyl]-7-nitro-

    Cas No: 104947-13-9

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104947-13-9 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 104947-13-9 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,0,4,9,4 and 7 respectively; the second part has 2 digits, 1 and 3 respectively.
Calculate Digit Verification of CAS Registry Number 104947-13:
(8*1)+(7*0)+(6*4)+(5*9)+(4*4)+(3*7)+(2*1)+(1*3)=119
119 % 10 = 9
So 104947-13-9 is a valid CAS Registry Number.

104947-13-9SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 13, 2017

Revision Date: Aug 13, 2017

1.Identification

1.1 GHS Product identifier

Product name (7-{(2S,3R)-2,3-Bis-[4-(1-ethoxy-ethoxy)-phenyl]-pentylsulfanyl}-heptyl)-(7-nitro-benzo[1,2,5]oxadiazol-4-yl)-amine

1.2 Other means of identification

Product number -
Other names -

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:104947-13-9 SDS

104947-13-9Relevant articles and documents

Preparation, Receptor Binding, and Fluorescence Properties of Hexestrol-Fluorophore Conjugates: Evaluation of Site of Attachment, Fluorophore Structure, and Fluorophore-Ligand Spacing

Fevig, Thomas L.,Lloyd, John E.,Zablocki, Jeffery A.,Katzenellenbogen, John A.

, p. 156 - 165 (2007/10/02)

We have undertaken a staged development of certain estrogen-fluorophore conjugates, in order to prepare a fluorescent estrogen suitable for determination of the estrogen receptor content of individual cells.Since non-steroidal estrogens with bulky substituents are often more readily bound by receptor than their steroidal counterparts, we have investigated fluorophore conjugates with derivatives of the non-steroidal estrogen hexestrol ((3R*,4S*)-3,4-bis(4-hydroxyphenyl)hexane).On the basis of the receptor-binding affinity of model compounds, we prepared a prototypical set of three ring- and side-chain-substituted fluorescent hexestrol derivatives, whose binding and fluorescence properties ultimately led to the preparation of a series of side-chain-substituted nitrobenzoxadiazole derivatives.The compounds prepared have binding affinities for the estrogen receptors that range from ca. 1percent to 5percent that of estradiol, and they have very favorable fluorescence characteristics, similar to those of fluorescein.

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