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(+/-)-2-(6-METHOXY-2-NAPHTHYL)PROPIONIC ACID is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

56547-15-0

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56547-15-0 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 56547-15-0 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 5,6,5,4 and 7 respectively; the second part has 2 digits, 1 and 5 respectively.
Calculate Digit Verification of CAS Registry Number 56547-15:
(7*5)+(6*6)+(5*5)+(4*4)+(3*7)+(2*1)+(1*5)=140
140 % 10 = 0
So 56547-15-0 is a valid CAS Registry Number.

56547-15-0SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 18, 2017

Revision Date: Aug 18, 2017

1.Identification

1.1 GHS Product identifier

Product name (2S)-2-(6-Methoxy-2-naphthyl)propanoic acid

1.2 Other means of identification

Product number -
Other names 6-Methoxy-2-naphthylaminomalonsaeurediaethylester

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:56547-15-0 SDS

56547-15-0Downstream Products

56547-15-0Relevant academic research and scientific papers

The Synthesis of Chiral α-Aryl α-Hydroxy Carboxylic Acids via RuPHOX-Ru Catalyzed Asymmetric Hydrogenation

Guo, Huan,Li, Jing,Liu, Delong,Zhang, Wanbin

, p. 3665 - 3673 (2017/09/11)

A ruthenocenyl phosphino-oxazoline-ruthenium complex (RuPHOX?Ru) catalyzed asymmetric hydrogenation of α-aryl keto acids has been successfully developed, affording the corresponding chiral α-aryl α-hydroxy carboxylic acids in high yields and with up to 97% ee. The reaction could be performed on a gram scale with a relatively low catalyst loading (up to 5000 S/C) and the resulting products can be transformed to several chiral building blocks, biologically active compounds and chiral drugs. (Figure presented.).

Alpha-acyl substituted naphthylacetic acids

-

, (2008/06/13)

Novel naphthylalkanoic acids and their derivatives are described. Therapeutic compositions and method of treatment of inflammation is also disclosed.

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