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4'-Bromo-4-(trifluoromethoxy)biphenyl, also known as TBMB, is a chemical compound that features a biphenyl molecule with a bromine atom at the 4' position and a trifluoromethoxy group at the 4-position. 4'-Bromo-4-(trifluoromethoxy)biphenyl is recognized for its strong electron-withdrawing properties and is valued for its unique structural features and synthetic versatility in the field of organic chemistry.

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  • 134150-03-1 Structure
  • Basic information

    1. Product Name: 4'-BROMO-4-(TRIFLUOROMETHOXY)BIPHENYL
    2. Synonyms: 4'-BROMO-4-(TRIFLUOROMETHOXY)BIPHENYL;4-BROMO-4'-TRIFLUOROMETHOXYDIPHENYL;4'-Bromo-4-(trifluoromethoxy)biphenyl 98%;4'-Bromo-4-(trifluoromethoxy)biphenyl98%
    3. CAS NO:134150-03-1
    4. Molecular Formula: C13H8BrF3O
    5. Molecular Weight: 317.1
    6. EINECS: N/A
    7. Product Categories: N/A
    8. Mol File: 134150-03-1.mol
  • Chemical Properties

    1. Melting Point: N/A
    2. Boiling Point: 190.5 °C at 760 mmHg
    3. Flash Point: 62.8 °C
    4. Appearance: /
    5. Density: 1.37 g/cm3
    6. Refractive Index: N/A
    7. Storage Temp.: N/A
    8. Solubility: N/A
    9. CAS DataBase Reference: 4'-BROMO-4-(TRIFLUOROMETHOXY)BIPHENYL(CAS DataBase Reference)
    10. NIST Chemistry Reference: 4'-BROMO-4-(TRIFLUOROMETHOXY)BIPHENYL(134150-03-1)
    11. EPA Substance Registry System: 4'-BROMO-4-(TRIFLUOROMETHOXY)BIPHENYL(134150-03-1)
  • Safety Data

    1. Hazard Codes: Xi
    2. Statements: 20/21/22-36/37/38
    3. Safety Statements: 26-36/37/39
    4. WGK Germany:
    5. RTECS:
    6. HazardClass: N/A
    7. PackingGroup: N/A
    8. Hazardous Substances Data: 134150-03-1(Hazardous Substances Data)

134150-03-1 Usage

Uses

Used in Organic Synthesis:
4'-Bromo-4-(trifluoromethoxy)biphenyl is used as a reagent for the synthesis of various organic compounds, particularly in the production of pharmaceuticals and agrochemicals. Its strong electron-withdrawing properties make it a valuable building block for creating biologically active compounds.
Used in Pharmaceutical Industry:
In the Pharmaceutical Industry, 4'-Bromo-4-(trifluoromethoxy)biphenyl is used as a precursor for the synthesis of drugs. Its unique structure allows for the development of new medicinal compounds with potential therapeutic applications.
Used in Agrochemical Industry:
4'-Bromo-4-(trifluoromethoxy)biphenyl is used as a starting material for the production of agrochemicals, contributing to the development of new pesticides and other agricultural chemicals to improve crop protection and yield.
Used in Metal-Catalyzed Reactions:
As a ligand in metal-catalyzed reactions, 4'-Bromo-4-(trifluoromethoxy)biphenyl is utilized to facilitate various chemical transformations, enhancing the efficiency and selectivity of these processes in organic synthesis.
Overall, 4'-Bromo-4-(trifluoromethoxy)biphenyl's diverse applications across different industries highlight its importance as a versatile and valuable tool in organic chemistry.

Check Digit Verification of cas no

The CAS Registry Mumber 134150-03-1 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,3,4,1,5 and 0 respectively; the second part has 2 digits, 0 and 3 respectively.
Calculate Digit Verification of CAS Registry Number 134150-03:
(8*1)+(7*3)+(6*4)+(5*1)+(4*5)+(3*0)+(2*0)+(1*3)=81
81 % 10 = 1
So 134150-03-1 is a valid CAS Registry Number.

134150-03-1SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 17, 2017

Revision Date: Aug 17, 2017

1.Identification

1.1 GHS Product identifier

Product name 1-bromo-4-[4-(trifluoromethoxy)phenyl]benzene

1.2 Other means of identification

Product number -
Other names PC2475

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:134150-03-1 SDS

134150-03-1Downstream Products

134150-03-1Relevant articles and documents

Photocatalyzed Transition-Metal-Free Oxidative Cross-Coupling Reactions of Tetraorganoborates**

Music, Arif,Baumann, Andreas N.,Boser, Florian,Müller, Nicolas,Matz, Florian,Jagau, Thomas C.,Didier, Dorian

supporting information, p. 4322 - 4326 (2021/02/11)

Readily accessible tetraorganoborate salts undergo selective coupling reactions under blue light irradiation in the presence of catalytic amounts of transition-metal-free acridinium photocatalysts to furnish unsymmetrical biaryls, heterobiaryls and arylated olefins. This represents an interesting conceptual approach to forge C?C bonds between aryl, heteroaryl and alkenyl groups under smooth photochemical conditions. Computational studies were conducted to investigate the mechanism of the transformation.

GLYCOLATE OXIDASE INHIBITORS FOR THE TREATMENT OF DISEASE

-

Paragraph 00488; 00489; 00931; 00932, (2021/01/22)

Described herein are compounds, methods of making such compounds, pharmaceutical compositions and medicaments containing such compounds, and methods of using such compounds to treat or prevent diseases or disorders associated with a defect in glyoxylate metabolism, for example a disease or disorder associated with the enzyme glycolate oxidase (GO) or alterations in oxalate metabolism. Such diseases or disorders include, for example, disorders of glyoxylate metabolism, including primary hyperoxaluria, that are associated with production of excessive amounts of oxalate.

GLYCOLATE OXIDASE INHIBITORS FOR THE TREATMENT OF DISEASE

-

Paragraph 00530; 00531; 00532; 00973; 009749; 00975, (2019/07/17)

Described herein are compounds, methods of making such compounds, pharmaceutical compositions and medicaments containing such compounds, and methods of using such compounds to treat or prevent diseases or disorders associated with the enzyme glycolate oxidase (GO). Such diseases or disorders include, for example, disorders of glyoxylate metabolism, including primary hyperoxaluria, that are associated with production of excessive amounts of oxalate.

C-Aryl glucoside SGLT2 inhibitors containing a biphenyl motif as potential anti-diabetic agents

Ding, Yuyang,Mao, Liufeng,Xu, Dengfeng,Xie, Hui,Yang, Ling,Xu, Hongjiang,Geng, Wenjun,Gao, Yong,Xia, Chunguang,Zhang, Xiquan,Meng, Qingyi,Wu, Donghai,Zhao, Junling,Hu, Wenhui

supporting information, p. 2744 - 2748 (2015/06/08)

A series of highly active C-aryl glucoside SGLT2 inhibitors containing a biphenyl motif were designed and synthesized for biological evaluation. Among the compounds tested, compound 16l demonstrated high inhibitory activity against SGLT2 (IC50 = 1.9 nM) with an excellent pharmacokinetic profile. Further study indicated that the in vivo efficacy of compound 16l was comparable to that of dapagliflozin, suggesting that further development would be worthwhile.

Liquid crystal compounds, liquid crystal medium and liquid crystal display

-

, (2008/06/13)

The instant invention relates to liquid crystal media comprising a strongly dielectrically positive component A, preferably comprising isothiocyanate compounds, most preferably compounds of formula I, as given in the text, and a further dielectrically positive component B, preferably comprising terminally polar substituted bi- or terphenyl compounds, most preferably comprising compounds of formula II, as given in the text, further to novel isothiocyanato compounds as well as to liquid crystal displays comprising these media, in particular to PDLC display and most particular to holographic PDLC displays. The instant invention further relates to compounds of formula I wherein the parameters are as as specified in the text.

A convenient synthesis of trifluoromethyl ethers by oxidative desulfurization-fluorination of dithiocarbonates

Kanie, Kiyoshi,Tanaka, Yoichiro,Suzuki, Kazundo,Kuroboshi, Manabu,Hiyama, Tamejiro

, p. 471 - 484 (2007/10/03)

Trifluoromethyl ethers R-OCF3 are easily synthesized from the corresponding dithiocarbonates R-OCS2Me (R = aryl or primary alkyl) by a reagent system consisting of 70% HF/pyridine and an N-halo imide. When the reaction is applied to R-OCS2Me wherein R = secondary alkyl, tertiary alkyl, or benzylic group, fluorination leading to the corresponding alkyl fluorides R-F is achieved, whereas a combination of 50% HF/pyridine and N- bromosuccinimide affords the corresponding trifluoromethyl ethers R-OCF3 (R = secondary).

Cyclic hydrocarbon derivative and liquid crystal composition containing the same

-

, (2008/06/13)

A cyclic hydrocarbon derivative represented by formula (I): STR1 wherein each of Y1 and Y2 is independently F, Cl, CN, OCN, SCN, OCF3, OCF2 H, OCF2 CF3, CF3, R, --OR, --COOR or --OCOR, wherein R is alkyl, alkenyl or alkoxyalkyl, provided that at least one of Y1 and Y2 is R, --OR, --COOR or --OCOR; each of Z, Z1, Z2, Z3 and Z4 is independently a single bond, --CH2 CH2 --, --CH=CH--, --C C--, --COO--, --OCO--, --CH2 O--, OCH2 --, --(CH2)4 --, --(CH2)3 --O-- or --O--(CH2)3 --; ring A is group of formula (II): STR2 wherein each of X1, X2, X3, X4, X5, X6, X7, X8, X9, and X10 is independently H or D, provided that at least one of them is D; each of rings K, L, J, M and N is independently trans-1,4-cyclohexylene, 1,4-cyclohexenylene, substituted trans-1,4-cyclohexylene, 1,4-phenylene, substituted 1,4-phenylene, 1,3-dioxane-2,6-diyl, pyrimidine-2,5-diyl, pyridine-2,5-diyl, pyarazine-2,5-diyl or a group of formula (III): STR3 wherein each of X11, X12, X13, X14, X15, X16, X17, X18, X19, and X20 is independently H or D, provided that at least one of them is D; in which the ring of formula (III) may be the same as or different from ring A; and k, l, m, and n each independently is 0 or 1, provided that the sum of k, l, m, and n is 0, 1 or 2. The compound is useful as an electro-optic liquid crystal display material.

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