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15258-73-8

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15258-73-8 Usage

Description

2,6-Dichlorobenzyl alcohol is an organic compound characterized by its white crystalline powder form. It is known for its reactivity and utility in various organic synthesis processes, making it a valuable component in the chemical industry.

Uses

Used in Organic Synthesis:
2,6-Dichlorobenzyl alcohol is used as a reagent in the chemical industry for its ability to participate in a wide range of organic synthesis reactions. Its chemical properties allow it to be a versatile building block for creating more complex molecules and compounds.
Used in Pharmaceutical Industry:
In the pharmaceutical industry, 2,6-Dichlorobenzyl alcohol is used as an intermediate in the synthesis of various drugs and medicinal compounds. Its unique structure and reactivity make it a valuable component in the development of new pharmaceuticals.
Used in Chemical Research:
2,6-Dichlorobenzyl alcohol is also utilized in chemical research as a model compound for studying reaction mechanisms and exploring new synthetic pathways. Its predictable and well-understood reactivity make it an ideal candidate for such investigations.
Used in Agrochemicals:
In the agrochemical industry, 2,6-Dichlorobenzyl alcohol is employed as a starting material for the synthesis of various agrochemicals, such as pesticides and herbicides. Its properties contribute to the development of effective and targeted products for agricultural use.
Used in Dyes and Pigments:
The chemical properties of 2,6-Dichlorobenzyl alcohol also make it suitable for use in the production of dyes and pigments. Its ability to form a variety of compounds allows for the creation of a wide range of colors and shades in the dye and pigment industry.

Synthesis Reference(s)

Tetrahedron Letters, 29, p. 707, 1988 DOI: 10.1016/S0040-4039(00)80190-2

Check Digit Verification of cas no

The CAS Registry Mumber 15258-73-8 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 1,5,2,5 and 8 respectively; the second part has 2 digits, 7 and 3 respectively.
Calculate Digit Verification of CAS Registry Number 15258-73:
(7*1)+(6*5)+(5*2)+(4*5)+(3*8)+(2*7)+(1*3)=108
108 % 10 = 8
So 15258-73-8 is a valid CAS Registry Number.
InChI:InChI=1/C7H6Cl2O/c8-6-2-1-3-7(9)5(6)4-10/h1-3,10H,4H2

15258-73-8 Well-known Company Product Price

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  • Alfa Aesar

  • (A12196)  2,6-Dichlorobenzyl alcohol, 99%   

  • 15258-73-8

  • 10g

  • 238.0CNY

  • Detail
  • Alfa Aesar

  • (A12196)  2,6-Dichlorobenzyl alcohol, 99%   

  • 15258-73-8

  • 50g

  • 856.0CNY

  • Detail

15258-73-8SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 20, 2017

Revision Date: Aug 20, 2017

1.Identification

1.1 GHS Product identifier

Product name 2,6-Dichlorobenzyl alcohol

1.2 Other means of identification

Product number -
Other names Benzenemethanol, 2,6-dichloro-

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:15258-73-8 SDS

15258-73-8Relevant articles and documents

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Castle,Riebsomer

, p. 142 (1956)

-

Hydrosilylation of aldehydes and ketones catalyzed by hydrido iron complexes bearing imine ligands

Zuo, Zhenyu,Sun, Hongjian,Wang, Lin,Li, Xiaoyan

, p. 11716 - 11722 (2014)

Two new hydrido iron complexes (2 and 4) were synthesized by the reactions of (4-methoxyphenyl)phenylketimine ((4-MeOPh)PhCNH) with Fe(PMe 3)4 or FeMe2(PMe3)4. The molecular structures of complexes 2 and 4 were confirmed by X-ray single crystal diffraction. Using hydrido iron complexes (1-4) as catalysts, the hydrosilylations of aldehydes and ketones were investigated. The four complexes were effective catalysts for this reduction reaction. Complex 1 among them is the best catalyst. This journal is the Partner Organisations 2014.

A tunable synthesis of either benzaldehyde or benzoic acid through blue-violet LED irradiation using TBATB

Mardani, Atefeh,Heshami, Marouf,Shariati, Yadollah,Kazemi, Foad,Abdollahi Kakroudi, Mazaher,Kaboudin, Babak

, (2019/11/29)

In this paper, a highly efficient, metal-free, and homogeneous method for the selective aerobic photooxidation of alcohols and photooxidative-desilylation of tert-butyldimethylsilyl ethers (TBDMS) in the presence of tetrabutylammonium tribromide (TBATB) under irradiation of visible light was reported. The light source: blue (460 nm) and violet (400 nm) LED, can control selective oxidation to aldehyde or carboxylic acid.

Pyridine: N-oxide promoted hydrosilylation of carbonyl compounds catalyzed by [PSiP]-pincer iron hydrides

Chang, Guoliang,Fenske, Dieter,Fuhr, Olaf,Li, Xiaoyan,Sun, Hongjian,Xie, Shangqing,Yang, Wenjing,Zhang, Peng

, p. 9349 - 9354 (2020/09/09)

Five [PSiP]-pincer iron hydrides 1-5, [(2-Ph2PC6H4)2HSiFe(H)(PMe3)2 (1), (2-Ph2PC6H4)2MeSiFe(H)(PMe3)2 (2), (2-Ph2PC6H4)2PhSiFe(H)(PMe3)2 (3), (2-(iPr)2PC6H4)2HSiFe(H)(PMe3) (4), and (2-(iPr)2PC6H4)2MeSiFe(H)(PMe3)2 (5)], were used as catalysts to study the effects of pyridine N-oxide and the electronic properties of [PSiP]-ligands on the catalytic hydrosilylation of carbonyl compounds. It was proved for the first time that this catalytic process could be promoted with pyridine N-oxide as the initiator at 30 °C because the addition of pyridine N-oxide is beneficial for the formation of an unsaturated hydrido iron complex, which is the key intermediate in the catalytic mechanism. Complex 4 as the best catalyst shows excellent catalytic performance. Among the five complexes, complex 3 was new and the molecular structure of complex 3 was determined by single crystal X-ray diffraction. A proposed mechanism was discussed.

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