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1,2-Naphthalenediol, 5,6,7,8-tetrahydro- is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

6255-90-9

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6255-90-9 Usage

Primary Use

Pharmaceutical industry

Type

Polyhydroxylated derivative of naphthalene

Antioxidant

Helps neutralize harmful free radicals and prevent cellular damage.

Anti-inflammatory

Reduces inflammation and swelling in the body.

Cancer treatment

May have potential in targeting cancer cells and reducing tumor growth.

Cardiovascular disease

Could help protect against heart and blood vessel damage.

Neurodegenerative disorders

May offer protection against damage to nerve cells and slow disease progression.

Check Digit Verification of cas no

The CAS Registry Mumber 6255-90-9 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 6,2,5 and 5 respectively; the second part has 2 digits, 9 and 0 respectively.
Calculate Digit Verification of CAS Registry Number 6255-90:
(6*6)+(5*2)+(4*5)+(3*5)+(2*9)+(1*0)=99
99 % 10 = 9
So 6255-90-9 is a valid CAS Registry Number.

6255-90-9SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 19, 2017

Revision Date: Aug 19, 2017

1.Identification

1.1 GHS Product identifier

Product name 1,2-dihydroxy-5,6,7,8-tetrahydronaphthalene

1.2 Other means of identification

Product number -
Other names 5,6-Dihydroxy-1,2,3,4-tetrahydronaphthalene

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:6255-90-9 SDS

6255-90-9Downstream Products

6255-90-9Relevant academic research and scientific papers

Cascade reaction of 2,3-naphthalenediol with benzene in the presence of aluminum halides

Zhu, Zhongwei,Salnikov, George E.,Koltunov, Konstantin Yu.

, p. 857 - 859 (2019)

2,3-Naphthalenediol on superelectrophilic activation with aluminium halides smoothly reacts with benzene to give 4-((3-phenyl-1H-inden-1-yl)methyl)benzene-1,2-diol, which in turn undergoes intramolecular cyclization to form 5,10-methano-5-phenyldibenzo[a,d]cycloheptane-2,3-diol. The mechanistic aspects of these unusual transformations are discussed.

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