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Methanone, [4-[(1R)-1-aminoethyl]phenyl]phenyl- is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

482620-70-2

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482620-70-2 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 482620-70-2 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 4,8,2,6,2 and 0 respectively; the second part has 2 digits, 7 and 0 respectively.
Calculate Digit Verification of CAS Registry Number 482620-70:
(8*4)+(7*8)+(6*2)+(5*6)+(4*2)+(3*0)+(2*7)+(1*0)=152
152 % 10 = 2
So 482620-70-2 is a valid CAS Registry Number.

482620-70-2SDS

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 [4-[(1R)-1-aminoethyl]phenyl]-phenylmethanone

1.2 Other means of identification

Product number -
Other names -

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:482620-70-2 SDS

482620-70-2Downstream Products

482620-70-2Relevant academic research and scientific papers

Studies on the enantioselective catalysis of photochemically promoted transformations: "Sensitizing receptors" as chiral catalysts

Cauble, David F.,Lynch, Vincent,Krische, Michael J.

, p. 15 - 21 (2003)

A strategy for the enantioselective catalysis of photomediated reactions in solution is described, involving the use of chiral molecular receptors possessing appendant triplet-sensitizing moieties. Energy transfer is selectively directed to bound substrate as a consequence of the distance dependence of triplet-triplet energy transfer. This effect, which is equivalent to a binding-induced rate enhancement, enables substoichiometric chirality transfer from the receptor template to the substrate, as observed in the intramolecular enone-olefin photo [2 + 2]cycloaddition of a quinolone substrate.

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