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6262-21-1

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6262-21-1 Usage

General Description

3,4,5,6-Tetrachlorofluorescein is a chemical compound with the molecular formula C20H8Cl4O5. It is a synthetic fluorescent dye used in various applications such as in biological and medical research, as well as in forensics. The compound is known for its bright yellow-green fluorescence and is commonly used as a tracer dye in various imaging techniques. 3,4,5,6-Tetrachlorofluorescein is also used as a pH indicator and in the production of colored plastics. However, it is important to handle this compound with caution as it is toxic and should only be used in a well-ventilated area by trained professionals.

Check Digit Verification of cas no

The CAS Registry Mumber 6262-21-1 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 6,2,6 and 2 respectively; the second part has 2 digits, 2 and 1 respectively.
Calculate Digit Verification of CAS Registry Number 6262-21:
(6*6)+(5*2)+(4*6)+(3*2)+(2*2)+(1*1)=81
81 % 10 = 1
So 6262-21-1 is a valid CAS Registry Number.
InChI:InChI=1/C20H8Cl4O5/c21-16-14(15(20(27)28)17(22)19(24)18(16)23)13-9-3-1-7(25)5-11(9)29-12-6-8(26)2-4-10(12)13/h1-6,25H,(H,27,28)

6262-21-1 Well-known Company Product Price

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  • Alfa Aesar

  • (B25635)  4,5,6,7-Tetrachlorofluorescein   

  • 6262-21-1

  • 1g

  • 382.0CNY

  • Detail
  • Alfa Aesar

  • (B25635)  4,5,6,7-Tetrachlorofluorescein   

  • 6262-21-1

  • 5g

  • 1170.0CNY

  • Detail

6262-21-1SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 12, 2017

Revision Date: Aug 12, 2017

1.Identification

1.1 GHS Product identifier

Product name 3,4,5,6-Tetrachlorofluorescein

1.2 Other means of identification

Product number -
Other names 4,5,6,7-tetrachloro-3',6'-dihydroxyspiro[2-benzofuran-3,9'-xanthene]-1-one

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:6262-21-1 SDS

6262-21-1Downstream Products

6262-21-1Relevant articles and documents

Ti(IV) doping: An effective strategy to boost Lewis acidic performance of ZnO catalyst in fluorescein dye synthesis

Jadhav, Nirajkumar H.,Shinde, Dnyaneshwar R.,Sakate, Sachin S.,Rasal, Nishant K.,Pawar, Ramdas A.

, p. 17 - 22 (2018/11/25)

Zn1-xTixO NPs were efficiently synthesized using a simple solution free mechanochemical method. The synthesized ZnO and Ti(IV)-doped ZnO catalysts are exhibited polycrystallinity, a hexagonal crystal structure, and roughly spherical agglomerates. The surface areas of the Zn1-xTixO catalysts were positively correlated with the doping percentage of Ti(IV), which also enhanced the Lewis acidity of the NPs. The catalysts exhibited excellent activity during the synthesis of fluorescein dyes. This methodology was also extended to sulfone-fluorescein dye synthesis.

PROCESS FOR THE SYNTHESIS OF 4,5,6,7-TETRACHLORO-3',6'-DIHYDROXY-2',4',5'7'-TETRAIODO-3H-SPIRO[ISOBENZOFURAN-1,9'-XANTHEN]-3-ONE (ROSE BENGAL) AND RELATED XANTHENES

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Paragraph 0065, (2015/11/10)

A new process for the manufacture of iodinated xanthenes in high purity includes a cyclization step followed by an iodination step. No extraction, chromatographic or solvent concentration steps are required, and the intermediate as well as final compounds are isolated via filtration or similar means. The process requires a single organic solvent, and the steps are completed at temperatures below 100° C. The exclusion of chloride ions, of chloride free-radicals, hypochlorite ions, or hypochlorous acid as reagents or from reagents that may generate these species in situ in the presence of oxidants, prevents undesirable impurity formation. Several new compounds have been conceived and isolated using these methods. These new compounds are also formed into new medicaments.

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