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2-Salicyloylbenzoic acid, also known as 2-salicyloylbenzoate, is an organic compound with the chemical formula C14H10O4. It is a white crystalline solid that is derived from the combination of salicylic acid and benzoic acid. 2-Salicyloylbenzoic acid is characterized by its ability to form complexes with various metal ions, which makes it useful in analytical chemistry for the detection and quantification of metals. It is also employed in the synthesis of pharmaceuticals and other organic compounds due to its reactive functional groups. The compound's structure features a salicyloyl group attached to a benzoic acid moiety, which contributes to its chemical reactivity and potential applications in various fields.

6079-73-8

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6079-73-8 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 6079-73-8 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 6,0,7 and 9 respectively; the second part has 2 digits, 7 and 3 respectively.
Calculate Digit Verification of CAS Registry Number 6079-73:
(6*6)+(5*0)+(4*7)+(3*9)+(2*7)+(1*3)=108
108 % 10 = 8
So 6079-73-8 is a valid CAS Registry Number.

6079-73-8SDS

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 2-hydroxybenzoylbenzoic acid

1.2 Other means of identification

Product number -
Other names 2-Salicyloyl-benzoesaeure

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:6079-73-8 SDS

6079-73-8Relevant academic research and scientific papers

Rational design of far red to near-infrared rhodamine analogues with huge Stokes shifts for single-laser excitation multicolor imaging

Zhang, Xingxing,Ren, Tianbing,Yang, Feiyu,Yuan, Lin

, p. 3890 - 3894 (2021)

Rhodamine dyes have been widely employed in biological imaging and sensing. However, it is always a challenge to design rhodamine derivatives with huge Stokes shift to address the draconian requirements of single-excitation multicolor imaging. In this work, we described a generally strategy to enhance the Stokes shift of rhodamine dyes by completely breaking their electronic symmetry. As a result, the Stokes shift of novel rhodamine dye DQF-RB-Cl is up to 205 nm in PBS, which is the largest in all the reported rhodamine derivatives. In addition, we successfully realized the single excitation trichromatic imaging of mitochondria, lysosomes and cell membranes by combining DQF-RB-Cl with commercial lysosomal targeting probe Lyso-Tracker Green and membrane targeting dye Dil. This is the organic synthetic dyes for SLE-trichromatic imaging in cells for the first time. These results demonstrate the potential of our design as a useful strategy to develop huge Stokes shift fluorophore for bioimaging.

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