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1,3-benzothiazol-2-yl(phenyl)methanol is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

22841-77-6

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22841-77-6 Usage

Family

Benzothiazole

Usage

Building block in organic synthesis and pharmaceutical research

Structural features

Benzothiazole ring with a phenylmethyl group attached

Versatility

Intermediate for the synthesis of various functionalized compounds

Applications

Pharmaceutical, agrochemical, and materials science development

Potential

Biological activities and interest in medicinal chemistry for new drug development

Check Digit Verification of cas no

The CAS Registry Mumber 22841-77-6 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 2,2,8,4 and 1 respectively; the second part has 2 digits, 7 and 7 respectively.
Calculate Digit Verification of CAS Registry Number 22841-77:
(7*2)+(6*2)+(5*8)+(4*4)+(3*1)+(2*7)+(1*7)=106
106 % 10 = 6
So 22841-77-6 is a valid CAS Registry Number.

22841-77-6SDS

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 1,3-benzothiazol-2-yl(phenyl)methanol

1.2 Other means of identification

Product number -
Other names 2-Benzothiazolylphenylmethanol

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:22841-77-6 SDS

22841-77-6Relevant academic research and scientific papers

One-pot synthesis of 2-acylbenzothiazoles from 2-aminobenzenethiols and arylacetonitriles via cyclization and sequential oxidation

Zhang, Shanshan,Wang, Shiwei,Leng, Yuting,Wu, Yangjie

supporting information, (2021/08/13)

An efficient one-pot method to access 2-acylbenzothiazoles via AlCl3-mediated cyclization reaction and I2-promoted sequential oxidation reaction of 2-aminobenzenethiols with arylacetonitriles was developed. This reaction proceeds smoothly with a wide range of arylacetonitriles containing different functional groups to give the corresponding products in moderate to good yields under mild conditions. Moreover, this reaction was conveniently conducted on a gram scale, and the yield is still up to 68%.

Synthesis of N-Formyl-2-benzoyl Benzothiazolines, 2-Substituted Benzothiazoles, and Symmetrical Disulfides from N-Phenacylbenzothiazolium Bromides

Sahoo, Subas Chandra,Pan, Subhas Chandra

supporting information, p. 6208 - 6212 (2019/08/21)

An unusual aerobic hydrolysis-cascade reaction has been developed with N-phenacylbenzothiazolium bromides by treatment with organic and inorganic base. The corresponding N-formyl-2-benzoyl benzothiazoline and 2-substituted benzothiazole products were obta

A removable functional group strategy for regiodivergent Wittig rearrangement products

Alam, Md Nirshad,Lakshmi,Maity, Pradip

supporting information, p. 8922 - 8926 (2018/12/10)

[1,2] and [2,3] Wittig rearrangements are competing reaction pathways, often leading to uncontrollable product distribution. We employ a single removable functional group to fulfill the dual role of attaining a reversible [2,3] and stabilizing radical int

Rhodium Catalyzed Asymmetric Hydrogenation of 2-Pyridine Ketones

Yang, Hailong,Huo, Ningning,Yang, Ping,Pei, Hao,Lv, Hui,Zhang, Xumu

, p. 4144 - 4147 (2015/09/15)

Catalyzed by [Rh(COD)Binapine]BF4, the asymmetric hydrogenation of 2-pyridine ketones has been achieved with excellent enantioselectivities (enantiomeric excesses up to 99%) under mild conditions. This method is suitable for various kinds of 2-pyridine ketones and their derivatives. A number of enantiomerically pure chiral 2-pyridine-aryl/alkyl alcohols were prepared through hydrogenation, which can be used directly in organic synthesis.

Bu4N+ alkoxide-initiated/autocatalytic addition reactions with organotrimethylsilanes

Das, Manas,O'Shea, Donal F.

, p. 5595 - 5607 (2014/07/08)

The use of Me3SiO-/Bu4N+ as a general activator of organotrimethylsilanes for addition reactions has been established. The broad scope of the method offers trimethylsilanes (including acetate, allyl, propargyl, benzyl, dithiane, heteroaryl, and aryl derivatives) as bench-stable organometallics that can be readily utilized as carbanion equivalents for synthesis. Reactions are achieved at rt without the requirement of specialized precautions that are commonplace for other organometallics.

Structures and reactivities of O-methylated Breslow intermediates

Maji, Biplab,Mayr, Herbert

supporting information, p. 10408 - 10412 (2012/11/07)

As close as you can get: Since Breslow intermediates usually exist in their keto form, their O-protected tautomers may be considered as their closest isolable relatives. A series of these compounds have been synthesized, their structures determined, and the kinetics of their reactions with electrophiles investigated. Copyright

BENZAZOLE DERIVATIVES AS HISTAMINE H4 RECEPTOR LIGANDS

-

Page/Page column 50, (2012/04/17)

The present patent application concerns new Iigands of the H4-receptor of formula (I), their process of preparation and their therapeutic use.

Benzazole derivatives as histamine H4 receptor ligands

-

Page/Page column 21, (2012/05/20)

The present patent application concerns new ligands of the H4-receptor of formula (I), their process of preparation and their therapeutic use.

PIPERAZINYL DERIVATIVES USEFUL AS MODULATORS OF THE NEUROPEPTIDE Y2 RECEPTOR

-

Page/Page column 73, (2009/07/18)

The present invention is directed to piperidinyl and piperazinyl derivatives of formula (II) useful as inhibitors of the NPY Y2 receptor, pharmaceutical compositions comprising said compounds, processes for the preparation of said compounds and the use of said compounds for the treatment and / or prevention of disorders, diseases and conditions mediated by the NPY Y2 receptor.

Stereoselective and competitive [1,2]- and [2,3]-wittig rearrangements of allyl heteroarylalkyl ethers

Capriati, Vito,Florio, Saverio,Ingrosso, Giovanni,Granito, Catia,Troisi, Luigino

, p. 478 - 484 (2007/10/03)

Several allyl heteroarylalkyl ethers have been synthesized and then deprotonated with nBuLi in THF at -78°C to give lithium derivatives. The lithium-bearing terminus was either the α- or the α′-carbon atom, depending on the associated proton acidity. In the absence of an external electrophile, a sigmatropic rearrangement occurs, generating a new C-C bond. Heteroarylalkyl homoallylic alcohols and allyl heteroarylalkylic alcohols were obtained as products of stereoselective [2,3]- or [1,2]-Wittig rearrangements, respectively. Homoallylic alcohols were obtained in high yields and with fairly good enantiomeric enrichments when the reactions were carried out in toluene with (-)-sparteine as the external chiral ligand.

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