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21389-90-2

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21389-90-2 Usage

Description

[1,1-Biphenyl]-2-ol,3,5-dimethyl-(9CI) is a chemical compound that belongs to the class of biphenyl compounds, which are aromatic hydrocarbons consisting of two phenyl rings connected by a single bond. This specific chemical is characterized by the presence of a hydroxyl group (-OH) attached to the second carbon of one of the phenyl rings, as well as two methyl groups (-CH3) at the 3rd and 5th positions of the other phenyl ring. It is commonly used in organic synthesis and chemical research as a building block for the preparation of more complex compounds. Additionally, it may have potential applications in the pharmaceutical and agrochemical industries, due to its unique chemical structure and properties. Overall, [1,1-Biphenyl]-2-ol,3,5-dimethyl-(9CI) is a versatile chemical compound with a range of potential uses in various scientific and industrial fields.

Uses

Used in Organic Synthesis:
[1,1-Biphenyl]-2-ol,3,5-dimethyl-(9CI) is used as a building block for the synthesis of more complex organic compounds. Its unique chemical structure allows for the creation of a variety of molecules with different properties and applications.
Used in Chemical Research:
[1,1-Biphenyl]-2-ol,3,5-dimethyl-(9CI) is used as a research tool in the field of chemistry to study the properties and reactions of biphenyl compounds. It can provide insights into the behavior of similar compounds and contribute to the development of new chemical processes and products.
Used in Pharmaceutical Industry:
[1,1-Biphenyl]-2-ol,3,5-dimethyl-(9CI) may be used as a starting material or intermediate in the development of new pharmaceutical compounds. Its unique structure could potentially be exploited to create novel drugs with specific therapeutic properties.
Used in Agrochemical Industry:
Similarly, this compound could be utilized in the development of new agrochemicals, such as pesticides or herbicides, due to its potential biological activity and unique chemical structure. Further research and development would be required to explore these applications fully.

Check Digit Verification of cas no

The CAS Registry Mumber 21389-90-2 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 2,1,3,8 and 9 respectively; the second part has 2 digits, 9 and 0 respectively.
Calculate Digit Verification of CAS Registry Number 21389-90:
(7*2)+(6*1)+(5*3)+(4*8)+(3*9)+(2*9)+(1*0)=112
112 % 10 = 2
So 21389-90-2 is a valid CAS Registry Number.

21389-90-2SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 15, 2017

Revision Date: Aug 15, 2017

1.Identification

1.1 GHS Product identifier

Product name 2,4-dimethyl-6-phenylphenol

1.2 Other means of identification

Product number -
Other names [1,1-biphenyl]-2-ol,3,5-dimethyl

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:21389-90-2 SDS

21389-90-2Downstream Products

21389-90-2Relevant articles and documents

Pentavalent Organobismuth Reagents. Part 2. The Phenylation of Phenols.

Barton, Derek H. R.,Bhatnagar, Neerja Yadav,Blazejewski, Jean-Claude,Charpiot, Brigitte,Finet, Jean-Pierre,et al.

, p. 2657 - 2666 (2007/10/02)

The phenylation of a variety of phenols by pentavalent bismuth reagents under neutral, acid and basic conditions has been investigated.Under basic conditions well defined pentavalent intermediates have been isolated and fully characterised.Their decomposition gives only ortho-C-phenylation (except in the case of a p-nitrophenol derivative).O-Phenylation is seen under neutral or acidic conditions.Another mechanism is proposed to explain this reaction with no pentavalent bismuth intermediate.

A Facile Synthesis of the Unsymmetrically Methyl-Substituted 2-Hydroxybiphenyls by Regioselective Cleavage of Dibenzofuran Derivatives with Lithium Metal

Keumi, Takashi,Murata, Chozo,Sasaki, Yasuto,Kitajima, Hidehiko

, p. 634 - 635 (2007/10/02)

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