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Benzenemethanol, 2-amino-α-(1-methylethyl)-α-phenyl-, also known as 2-amino-2-phenylbutan-1-ol or α-phenyl-2-amino-2-methyl-1-butanol, is an organic compound with the chemical formula C11H17NO. It is a derivative of benzyl alcohol, featuring an amino group at the 2-position and an isopropyl group at the α-position. Benzenemethanol, 2-amino-a-(1-methylethyl)-a-phenyl- is a chiral molecule, meaning it has a non-superimposable mirror image, and is used as an intermediate in the synthesis of various pharmaceuticals and agrochemicals. Its structure consists of a benzene ring attached to a secondary alcohol with an amino group and an isopropyl group, which contributes to its unique chemical properties and reactivity.

27309-56-4

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27309-56-4 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 27309-56-4 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 2,7,3,0 and 9 respectively; the second part has 2 digits, 5 and 6 respectively.
Calculate Digit Verification of CAS Registry Number 27309-56:
(7*2)+(6*7)+(5*3)+(4*0)+(3*9)+(2*5)+(1*6)=114
114 % 10 = 4
So 27309-56-4 is a valid CAS Registry Number.

27309-56-4SDS

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 (+-)-1-<2-Amino-phenyl>-2-methyl-1-phenyl-propan-1-ol

1.2 Other means of identification

Product number -
Other names (+-)-1-(2-Amino-phenyl)-2-methyl-1-phenyl-propan-1-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:27309-56-4 SDS

27309-56-4Relevant academic research and scientific papers

Thermal induced intramolecular [2 + 2] cycloaddition of allene-ACPs

Chen, Kai,Sun, Run,Xu, Qin,Wei, Yin,Shi, Min

supporting information, p. 3949 - 3953 (2013/07/05)

A facile synthetic method for preparation of bicyclo[4.2.0] nitrogen heterocycles has been developed via a thermal induced intramolecular [2 + 2] cycloaddition reaction of allene-ACPs. The DFT calculations indicate that this intramolecular cycloaddition proceeds in a concerted manner and a strained small ring is essential. The Royal Society of Chemistry 2013.

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