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2-Benzothiazoleethanol,alpha-(1-methylethyl)-(9CI) is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

107401-57-0

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107401-57-0 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 107401-57-0 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,0,7,4,0 and 1 respectively; the second part has 2 digits, 5 and 7 respectively.
Calculate Digit Verification of CAS Registry Number 107401-57:
(8*1)+(7*0)+(6*7)+(5*4)+(4*0)+(3*1)+(2*5)+(1*7)=90
90 % 10 = 0
So 107401-57-0 is a valid CAS Registry Number.

107401-57-0SDS

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-(benzo[d]thiazol-2-yl)-3-methylbutan-2-ol

1.2 Other means of identification

Product number -
Other names 1-Benzothiazol-2-yl-3-methyl-butan-2-ol

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:107401-57-0 SDS

107401-57-0Downstream Products

107401-57-0Relevant academic research and scientific papers

Samarium Barbier reactions of α-iodomethyloxazoles and thiazoles with aliphatic aldehydes

Williams, David R.,Berliner, Martin A.,Stroup, Bryan W.,Nag, Partha P.,Clark, Michael P.

, p. 4099 - 4102 (2007/10/03)

(Chemical Equation Presented) The reductive coupling of substituted α-iodomethyloxazoles and thiazoles with aliphatic aldehydes under Barbier conditions provides an effective method for the direct incorporation of intact heterocyclic systems.

Samarium diiodide mediated barbier-type reaction of 2-chloromethylbenzoxazole and 2-chloromethylbenzothiazole with carbonyl compounds: A convenient synthesis of 1-(β-hydroxyalkyl)benzoxazoles and 1-(β-hydroxyalkyl)benzothiazoles

Xu, Xiaoliang,Zhang, Yongmin

, p. 3551 - 3559 (2007/10/03)

1-(β-Hydroxyalkyl)benzoxazoles and 1-(β -hydroxyalkyl)benzothiazoles were prepared via reductive addition reactions of 2-chloromethylbenzoxazole and 2-chloromethylbenzothiazole with carbonyl compounds under mild conditions mediated by SmI2.

General Method for an Aldol-Type Reaction of 2-Methylbenzothiazole with Carbonyl Compounds

Chikashita, Hidenori,Ikegami, Seiji,Okumura, Takeshi,Itoh, Kazuyoshi

, p. 375 - 377 (2007/10/02)

A general and versatile method for the preparation of a variety of β-hydroxybenzothiazoles (aldol-type adducts) by the reaction of α-lithio-2-methylbenzothiazole with carbonyl compounds was proposed.As an example of the use of α-lithio-2-methylbenzothiazo

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