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7089-34-1

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7089-34-1 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 7089-34-1 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 7,0,8 and 9 respectively; the second part has 2 digits, 3 and 4 respectively.
Calculate Digit Verification of CAS Registry Number 7089-34:
(6*7)+(5*0)+(4*8)+(3*9)+(2*3)+(1*4)=111
111 % 10 = 1
So 7089-34-1 is a valid CAS Registry Number.

7089-34-1SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 17, 2017

Revision Date: Aug 17, 2017

1.Identification

1.1 GHS Product identifier

Product name (3-dimethylamino-2-phenylprop-2-enylidene)dimethylammonium perchlorate

1.2 Other means of identification

Product number -
Other names 1-Dimethylamino-3-dimethylimonio-2-phenyl-propen-(1)-perchlorat

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:7089-34-1 SDS

7089-34-1Relevant articles and documents

A facile and efficient route to one-pot synthesis of new cyclophanes using vinamidinium salts

Golzar, Nooshin,Mehranpour, Abdolmohammad,Nowrouzi, Najmeh

, p. 13666 - 13673 (2021)

In this study, an efficient method for the synthesis of new cyclophanes (5a-f,6a-g) through the condensation of 1,4-phenylenedimethanamine (3) or 2,3,5,6-tetramethylbenzene-1,4-diamine (4) with 2-substituted vinamidiniums (2a-g) is described. The cyclopha

Synthesis of new metal-free 1,2,4,5,9,10,12,13-octaaza[16]annulene derivatives using the reaction of vinamidinium salts with thiocarbohydrazide

Sabet, Askar,Mehranpour, Abdolmohammad

, p. 833 - 840 (2021/01/12)

A new series of marcocyclic ligands, 1,2,4,5,9,10,12,13-octaaza[16]annulene derivatives were synthesized by using the condensation reaction of the correspondingly [2+2] 2-heteroaryl-substituted vinamidinium salts or phenyl vinamidinium salts and derivativ

S - Cis Diene Conformation: A New Bathochromic Shift Strategy for Near-Infrared Fluorescence Switchable Dye and the Imaging Applications

Chen, Hsiang-Jung,Chew, Chee Ying,Chang, En-Hao,Tu, Yu-Wei,Wei, Li-Yu,Wu, Bo-Han,Chen, Chien-Hung,Yang, Ya-Ting,Huang, Su-Chin,Chen, Jen-Kun,Chen, I-Chia,Tan, Kui-Thong

supporting information, p. 5224 - 5234 (2018/04/23)

In this paper, we present a novel charge-free fluorescence-switchable near-infrared (IR) dye based on merocyanine for target specific imaging. In contrast to the typical bathochromic shift approach by extending π-conjugation, the bathochromic shift of our merocyanine dye to the near-IR region is due to an unusual S-cis diene conformer. This is the first example where a fluorescent dye adopts the stable S-cis conformation. In addition to the novel bathochromic shift mechanism, the dye exhibits fluorescence-switchable properties in response to polarity and viscosity. By incorporating a protein-specific ligand to the dye, the probes (for SNAP-tag and hCAII proteins) exhibited dramatic fluorescence increase (up to 300-fold) upon binding with its target protein. The large fluorescence enhancement, near-IR absorption/emission, and charge-free scaffold enabled no-wash and site-specific imaging of target proteins in living cells and in vivo with minimum background fluorescence. We believe that our unconventional approach for a near-IR dye with the S-cis diene conformation can lead to new strategies for the design of near-IR dyes.

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