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GRI 378898, also known as 1,2,3,4,5,6-hexafluorobenzene, is an organic compound with the chemical formula C6F6. It is a colorless, volatile liquid that is widely used as a solvent and a chemical intermediate in the synthesis of various pharmaceuticals, agrochemicals, and specialty chemicals. Due to its unique properties, such as high thermal stability, low reactivity, and excellent dielectric constant, GRI 378898 has found applications in the electronics industry as well. It is also used as a building block for the production of other fluorinated compounds, making it an important chemical in the field of fluorochemistry.

2805-76-7

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2805-76-7 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 2805-76-7 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 2,8,0 and 5 respectively; the second part has 2 digits, 7 and 6 respectively.
Calculate Digit Verification of CAS Registry Number 2805-76:
(6*2)+(5*8)+(4*0)+(3*5)+(2*7)+(1*6)=87
87 % 10 = 7
So 2805-76-7 is a valid CAS Registry Number.

2805-76-7Relevant academic research and scientific papers

Enantioselective Strecker and Allylation Reactions with Aldimines Catalyzed by Chiral Oxazaborolidinium Ions

Kang, Ki-Tae,Park, Sang Hyun,Ryu, Do Hyun

supporting information, p. 6679 - 6683 (2019/09/12)

Chiral oxazaborolidinium ion (COBI)-catalyzed enantioselective nucleophilic addition reactions of aldimines using tributyltin cyanide and allyltributylstannane have been developed. Various α-aminonitriles and homoallylic amines were synthesized in high yi

Microwave-assisted synthesis of substituted dibenzo[b,f][1,4]thiazepines, dibenzo[b,f][1,4]oxazepines, benzothiazoles, and benzimidazoles

Lin, Yu-Chin,Li, Ni-Ching,Cherng, Yie-Jia

, p. 808 - 814 (2014/06/10)

A highly efficient synthesis for possessing 7-membered rings with two heteroatoms is described, using efficient microwave-assisted one-pot method to synthesize (substituted) dibenzo[b,f][1,4]thiazepines [1] and dibenzo[b,f][1,4]oxazepines [2] in high yields (up to 99%) by cyclocondensations of o-aminothiophenol or o-aminophenol with o-halobenzaldehydes, o-fluoroacetophenone, and o-fluorobenzophenone. In the absence of base, o-aminothiophenol reacted with o-halobenzaldehydes to afford benzothiazoles.

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