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METHYL 4'-HYDROXY[1,1'-BIPHENYL]-4-CARBOXYLATE, with the molecular formula C15H12O3, is a versatile chemical compound that serves as a key intermediate in the synthesis of pharmaceuticals, agrochemicals, and organic compounds. Its structural properties make it a valuable building block for various chemical synthesis processes, contributing to the development of new compounds with potential therapeutic properties.

40501-41-5

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40501-41-5 Usage

Uses

Used in Pharmaceutical Industry:
METHYL 4'-HYDROXY[1,1'-BIPHENYL]-4-CARBOXYLATE is used as a key intermediate for the synthesis of various drugs, contributing to the development of new compounds with potential therapeutic properties. Its ability to act as a building block in chemical synthesis processes makes it an important raw material in the production of pharmaceuticals.
Used in Agrochemical Industry:
METHYL 4'-HYDROXY[1,1'-BIPHENYL]-4-CARBOXYLATE is used as a raw material in the manufacturing of agrochemicals, where it can be employed in the creation of new compounds with potential applications in agriculture, such as pesticides or herbicides.
Used in Chemical Industry:
METHYL 4'-HYDROXY[1,1'-BIPHENYL]-4-CARBOXYLATE is used as a versatile chemical compound in the production of various industrial chemicals, further expanding its applications and demonstrating its value in diverse chemical synthesis processes.

Check Digit Verification of cas no

The CAS Registry Mumber 40501-41-5 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 4,0,5,0 and 1 respectively; the second part has 2 digits, 4 and 1 respectively.
Calculate Digit Verification of CAS Registry Number 40501-41:
(7*4)+(6*0)+(5*5)+(4*0)+(3*1)+(2*4)+(1*1)=65
65 % 10 = 5
So 40501-41-5 is a valid CAS Registry Number.

40501-41-5SDS

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 methyl 4-(4-hydroxyphenyl)benzoate

1.2 Other means of identification

Product number -
Other names 4'-hydroxy[1,1'-biphenyl]-4-carboxylic acid methyl ester

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:40501-41-5 SDS

40501-41-5Relevant academic research and scientific papers

Mechanisms of the photochemical rearrangement of diphenyl ethers

Haga, Naoki,Takayanagi, Hiroaki

, p. 735 - 745 (2007/10/03)

The mechanism of the photochemical rearrangement of diphenyl ether (1a) was studied. Irradiation of 1a in ethanol gave 2-phenylphenol (2, 42%) and 4-phenylphenol (3, 11%) as rearrangement products, in addition to phenol (4, 30%) and benzene (5, 25%) as diffusion products. Cross-coupling experiments employing [2H10]1a demonstrated that the formation of 2- and 4-phenylphenol was an intramolecular process. Irradiation of 1a in benzene or in toluene gave biphenyls in good yields. The combined yields of rearrangement products (2 and 3) increased with increase of solvent viscosity, with a concomitant decrease in the formation of 4. All the results can be rationalized in terms of excitation of 1a to the singlet state and dissociation to a radical pair intermediate involving phenoxy and phenyl radicals. Intramolecular recombination of these radicals gives rearrangement products, and escape followed by hydrogen abstraction from the solvent gives diffusion products. When position 4 of 1a was occupied by an electron-donating substituent (1b-e), aryloxy-phenyl bond cleavage to give the corresponding rearrangement products prevailed over phenoxy-aryl bond cleavage. The opposite was the case for substrates with an electron-withdrawing substituent at position 4 (1h,i).

Mesomorphic Properties of n-Alkyl-4'-n-Pentanoyloxy-Biphenyl-4-Carboxylates

Surendranath, V.,Fishel, D. L.,Vries, A de,Mahmood, R.,Johnson, D. L.

, p. 1 - 8 (2007/10/02)

Esters in the homologous series n-alkyl-4'-n-pentanoyloxy-biphenyl-4-carboxylates (n4COOBC, n=1-12) have been synthesized.Mesomorphic properties and phase transitions have been determined using polarizing hot-stage microscopy, DSC and x-ray.Phase transitions from SA-SB crystal and hexatic (tentatively) have been observed.The relationship between the incidence of hexatic phase and molecular structure has been discussed.

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