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5,6-Dibromo-indan-2-ol is a chemical compound with the molecular formula C9H7Br2OH. It is a white to off-white solid with a melting point of around 103-105°C. This brominated compound is characterized by the presence of bromine atoms and is used as a building block in the production of other chemical compounds, as well as in various organic synthesis reactions.
Used in Organic Synthesis:
5,6-Dibromo-indan-2-ol is used as a key intermediate in organic synthesis for the production of a variety of chemical compounds. Its unique structure and reactivity make it a valuable component in creating new molecules with specific properties.
Used in Pharmaceutical Industry:
In the pharmaceutical industry, 5,6-Dibromo-indan-2-ol is utilized as a building block for the synthesis of pharmaceutical intermediates. These intermediates are essential in the development of new drugs and medications, contributing to advancements in healthcare and medicine.
It is important to handle 5,6-Dibromo-indan-2-ol with care, as brominated compounds can be toxic and may have environmental implications. Proper safety measures should be taken during its use to minimize any potential risks.

862135-56-6

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862135-56-6 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 862135-56-6 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 8,6,2,1,3 and 5 respectively; the second part has 2 digits, 5 and 6 respectively.
Calculate Digit Verification of CAS Registry Number 862135-56:
(8*8)+(7*6)+(6*2)+(5*1)+(4*3)+(3*5)+(2*5)+(1*6)=166
166 % 10 = 6
So 862135-56-6 is a valid CAS Registry Number.

862135-56-6Downstream Products

862135-56-6Relevant academic research and scientific papers

Concise syntheses of 2-aminoindans via indan-2-ol

G?ksu, Süleyman,Se?en, Hasan

, p. 6801 - 6807 (2005)

2-Amino-5,6-dimethoxyindan hydrochloride was synthesized in seven steps and with an overall yield of 48%. Indan-2-ol was converted to 5,6-dibromo-indan-2- ol in three steps by acetylation, electrophilic bromination and deacetylation. Dimethoxylation of 5,6-dibromoindan-2-ol with NaOCH3 in the presence of CuI gave 5,6-dimethoxy-indan-2-ol, which was converted to 2-amino-5,6-dimethoxyindan hydrochloride by azidation, followed by Pd-C catalyzed hydrogenation. Similarly, 2-amino-5-bromoindan was synthesized in five steps and with an overall yield of 50%. Indan-2-ol was converted to 2-aminoindan by azidation followed by Pd-C catalyzed hydrogenation. The reaction of 2-aminoindan with 2.5 equiv Br2 afforded 2-amino-5,6- dibromoindan.

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