What is the alpha-(bromomethyl)benzyl alcohol?

alpha-(bromomethyl)benzyl alcohol is , while it's Molecular Formula is C8H9 Br O. Used in Pharmaceutical Synthesis: Alpha-(bromomethyl)benzyl alcohol is used as a key intermediate in the synthesis of pharmaceuticals for its ability to facilitate the creation of complex molecular structures. Its reactivity in forming carbon-carbon and carbon-oxygen bonds is particularly valuable in the development of new drugs. Used in Agrochemical Production: In the agrochemical industry, alpha-(bromomethyl)benzyl alcohol is employed as a building block for the synthesis of various agrochemicals, contributing to the development of effective compounds for crop protection and enhancement of agricultural productivity. Used in Organic Synthesis as a Reagent: Alpha-(bromomethyl)benzyl alcohol serves as a reagent in organic synthesis, where it is instrumental in the formation of essential carbon-carbon and carbon-oxygen bonds, which are fundamental in constructing a wide range of organic molecules. Safety Considerations: Given its classification as a hazardous chemical, alpha-(bromomethyl)benzyl alcohol requires careful handling to prevent skin and eye irritation. Additionally, it poses toxic risks if ingested or inhaled, necessitating proper safety measures during its use in laboratories and industrial settings.

What is the CAS number for alpha-(bromomethyl)benzyl alcohol?

The CAS number of alpha-(bromomethyl)benzyl alcohol is 2425-28-7.

What is alpha-(bromomethyl)benzyl alcohol (2425-28-7) used for?

Alpha-(bromomethyl)benzyl alcohol is a chemical compound with the molecular formula C8H9BrO. It is an organic compound that features a benzyl group with a bromomethyl group and a hydroxyl group at the alpha position. alpha-(bromomethyl)benzyl alcohol is recognized for its role as a building block in the synthesis of various organic compounds, including pharmaceuticals and agrochemicals, and is utilized as a reagent in organic synthesis for forming carbon-carbon and carbon-oxygen bonds.InChI:InChI=1/C8H9BrO/c9-6-8(10)7-4-2-1-3-5-7/h1-5,8,10H,6H2/t8-/m1/s1

What is the alpha-(bromomethyl)benzyl alcohol?

alpha-(bromomethyl)benzyl alcohol is , while it's Molecular Formula is C8H9 Br O. Used in Pharmaceutical Synthesis: Alpha-(bromomethyl)benzyl alcohol is used as a key intermediate in the synthesis of pharmaceuticals for its ability to facilitate the creation of complex molecular structures. Its reactivity in forming carbon-carbon and carbon-oxygen bonds is particularly valuable in the development of new drugs. Used in Agrochemical Production: In the agrochemical industry, alpha-(bromomethyl)benzyl alcohol is employed as a building block for the synthesis of various agrochemicals, contributing to the development of effective compounds for crop protection and enhancement of agricultural productivity. Used in Organic Synthesis as a Reagent: Alpha-(bromomethyl)benzyl alcohol serves as a reagent in organic synthesis, where it is instrumental in the formation of essential carbon-carbon and carbon-oxygen bonds, which are fundamental in constructing a wide range of organic molecules. Safety Considerations: Given its classification as a hazardous chemical, alpha-(bromomethyl)benzyl alcohol requires careful handling to prevent skin and eye irritation. Additionally, it poses toxic risks if ingested or inhaled, necessitating proper safety measures during its use in laboratories and industrial settings.

What is the CAS number for alpha-(bromomethyl)benzyl alcohol?

The CAS number of alpha-(bromomethyl)benzyl alcohol is 2425-28-7.

What is alpha-(bromomethyl)benzyl alcohol (2425-28-7) used for?

Alpha-(bromomethyl)benzyl alcohol is a chemical compound with the molecular formula C8H9BrO. It is an organic compound that features a benzyl group with a bromomethyl group and a hydroxyl group at the alpha position. alpha-(bromomethyl)benzyl alcohol is recognized for its role as a building block in the synthesis of various organic compounds, including pharmaceuticals and agrochemicals, and is utilized as a reagent in organic synthesis for forming carbon-carbon and carbon-oxygen bonds.InChI:InChI=1/C8H9BrO/c9-6-8(10)7-4-2-1-3-5-7/h1-5,8,10H,6H2/t8-/m1/s1

Home > Others

Others

Product classification

Contact us

alpha-(bromomethyl)benzyl alcohol

CAS：2425-28-7
purity：99%

Inquiry

alpha-(bromomethyl)benzyl alcohol 2425-28-7 with purity >99% Low price in stock

Molecular Formula: C8H9 Br O
Molecular Weight: 201.063
Vapor Pressure: 0.00578mmHg at 25°C
Melting Point: 39°C
Refractive Index: 1.5800 (estimate)
Boiling Point: 261.6°Cat760mmHg
PKA: 13.00±0.20(Predicted)
Flash Point: 135.6°C
PSA： 20.23000
Density: 1.503g/cm³
LogP: 2.11490

alpha-(bromomethyl)benzyl alcohol(Cas 2425-28-7) Usage

General Description

Alpha-(bromomethyl)benzyl alcohol is a chemical compound with the molecular formula C8H9BrO. It is an organic compound that contains a benzyl group substituted with a bromomethyl group and a hydroxyl group at the alpha position. alpha-(bromomethyl)benzyl alcohol is commonly used as a building block in the synthesis of pharmaceuticals, agrochemicals, and other organic compounds. It is also used as a reagent in organic synthesis, particularly in the formation of carbon-carbon and carbon-oxygen bonds. Alpha-(bromomethyl)benzyl alcohol is considered to be a hazardous chemical and should be handled with care due to its potential to cause skin and eye irritation and its toxic effects if ingested or inhaled.

InChI:InChI=1/C8H9BrO/c9-6-8(10)7-4-2-1-3-5-7/h1-5,8,10H,6H2/t8-/m1/s1

2425-28-7 Relevant articles

-

Buckles,Maurer

, p. 1585,1587 (1953)

An 18O-Labeling Study of the β-(Nitroxy)alkyl and β-(Trifluoroacetoxy)alkyl Radical Migrations: Further Examples of a 1,2-Shift Mechanism

Crich, David,Filzen, G. Frederick

, p. 4834 - 4837 (1995)

The results of an 18O labeling study of ...

Metalated Ir–CNP Complexes Containing Imidazolin-2-ylidene and Imidazolidin-2-ylidene Donors – Synthesis, Structure, Luminescence, and Metal–Ligand Cooperative Reactivity

Hernández-Juárez, Martín,Sánchez, Práxedes,López-Serrano, Joaquín,Lara, Patricia,González-Herrero, Pablo,Rendón, Nuria,álvarez, Eleuterio,Paneque, Margarita,Suárez, Andrés

, p. 3944 - 3953 (2020)

The iridium complex 1 based on a metalat...

A vanadium-dependent bromoperoxidase in the marine red alga Kappaphycus alvarezii (Doty) Doty displays clear substrate specificity

Kamenarska, Zornitsa,Taniguchi, Tomokazu,Ohsawa, Noboru,Hiraoka, Masanori,Itoh, Nobuya

, p. 1358 - 1366 (2007)

Bromoperoxidase activity was initially d...

In situ NMR study of asymmetric borane reduction reaction - An abnormal factor in the temperature effect on the bis-oxazaborolidine catalyst and the relationship between the catalyst structure and selectivity

Zhao, Jinkai,Bao, Xinhe,Liu, Xiumei,Wan, Boshun,Han, Xiuwen,Yang, Caiguang,Hang, Jiangfeng,Feng, Yan,Jiang, Biao

, p. 3351 - 3359 (2000)

The relationship between the structure o...

A highly regio- and chemoselective synthesis of vicinal bromohydrins by ring opening of terminal epoxides with dibromoborane-dimethyl sulfide

Roy, Chandra D.,Brown, Herbert C.

, p. 1608 - 1613 (2007)

Dibromoborane-dimethyl sulfide (BHBr2-SM...

New chiral borohydride based reducing agent: Asymmetric reduction of 9-anthryl trifluoromethyl ketone and other carbonyl compounds

Maiti, Dilip K.,Bhattacharya, Pranab K.

, p. 99 - 108 (1998)

(S)-(+)-2-(α-Hydroxybenzyl)benzimidazole...

Asymmetric hydrolysis of (dl)-1-acyloxy-2-halo-1-phenylethanes with lipases

Kutsuki,Sawa,Hasegawa,Watanabe

, p. 2369 - 2373 (1986)

Enantioselective borane reduction of aromatic ketones catalyzed by chiral aluminum alkoxides

Fu, I.-Pin,Uang, Biing-Jiun

, p. 45 - 48 (2001)

The asymmetric borane reduction of proch...

Regio- and stereoselective synthesis of bromoalkenes by homolytic hydrobromination of alkynes with hydrogen bromide

Kumaki, Wataru,Kinoshita, Hidenori,Miura, Katsukiyo

supporting information, (2022/03/07)

Homolytic hydrobromination of terminal a...

Unmasking the Hidden Carbonyl Group Using Gold(I) Catalysts and Alcohol Dehydrogenases: Design of a Thermodynamically-Driven Cascade toward Optically Active Halohydrins

Escot, Lorena,González-Granda, Sergio,Gotor-Fernández, Vicente,Lavandera, Iván

, p. 2552 - 2560 (2022/02/16)

A concurrent cascade combining the use o...

Chiral salen - Ni (II) based spherical porous silica as platform for asymmetric transfer hydrogenation reaction and synthesis of potent drug intermediate montekulast

Shukla, Meenakshi,Barick,Salunke,Chandra, Sudeshna

, (2021/02/05)

Heterogeneous catalyst has an edge over ...

Alkene, Bromide, and ROH – How To Achieve Selectivity? Electrochemical Synthesis of Bromohydrins and Their Ethers

Bityukov, Oleg V.,Nikishin, Gennady I.,Terent'ev, Alexander O.,Vil', Vera A.

supporting information, p. 3070 - 3078 (2021/05/10)

Bromohydrins and their ethers were elect...

2425-28-7 Process route

: 70-11-1
α-bromoacetophenone

: 13367-81-2
10-methylacridinium cation

: 98-85-1,13323-81-4
1-Phenylethanol

: 2425-28-7
2-Bromo-1-phenylethanol

: 98-86-2
acetophenone

Conditions

Conditions	Yield
With perchloric acid; 9,10-dihydro-10-methylacridine; In [D₃]acetonitrile; at 61.9 ℃; for 11h; Title compound not separated from byproducts;	14 % Spectr. 82 % Spectr. 100 % Spectr. 4 % Spectr.

: methyllithium lithium bromide

: 1620586-86-8
tri-n-butylstannylmethylfluoride

: 100-52-7
benzaldehyde

: 96-09-3
styrene oxide

: 98-85-1,13323-81-4
1-Phenylethanol

: 2425-28-7
2-Bromo-1-phenylethanol

: 450-94-2
2-fluoro-1-phenylethanol

: 1528-01-4
methyltributyltin