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113546-05-7

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113546-05-7 Usage

Molecular weight

154.23 g/mol

Physical state

Colorless liquid

Odor

Mild, sweet, and alcohol-like

Functional groups

Thiophene ring, propan-2-ol group

Usage

Flavoring agent, fragrance ingredient, intermediate in organic synthesis

Industries

Food, perfume, pharmaceuticals

Pharmacological properties

Potential therapeutic effects

Interest in fields

Medicinal chemistry, drug development

Check Digit Verification of cas no

The CAS Registry Mumber 113546-05-7 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,1,3,5,4 and 6 respectively; the second part has 2 digits, 0 and 5 respectively.
Calculate Digit Verification of CAS Registry Number 113546-05:
(8*1)+(7*1)+(6*3)+(5*5)+(4*4)+(3*6)+(2*0)+(1*5)=97
97 % 10 = 7
So 113546-05-7 is a valid CAS Registry Number.

113546-05-7SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 19, 2017

Revision Date: Aug 19, 2017

1.Identification

1.1 GHS Product identifier

Product name 2-thiophen-3-ylpropan-2-ol

1.2 Other means of identification

Product number -
Other names 2-(thiophen-3-yl)propan-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:113546-05-7 SDS

113546-05-7Downstream Products

113546-05-7Relevant articles and documents

Zinc(ii)-catalyzed Grignard additions to ketones with RMgBr and RMgI

Hatano, Manabu,Ito, Orie,Suzuki, Shinji,Ishihara, Kazuaki

supporting information; experimental part, p. 2674 - 2676 (2010/07/08)

Highly efficient alkylations and arylations of ketones with Grignard reagents (RMgBr and RMgI) have been developed using catalytic ZnCl2, Me3SiCH2MgCl, and LiCl. Tertiary alcohols were obtained in high yields with high chemoselectivities, while minimizing undesired side products produced by reduction and enolization.

Unsaturated Heterocyclic Amines as Potent Time-Dependent Inhibitors of Dopamine β-Hydroxylase

Bargar, Thomas M.,Broersma, Robert J.,Creemer, Lawrence C.,McCarthy, James R.,Hornsperger, Jean-Marie,et al.

, p. 315 - 317 (2007/10/02)

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