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2-Methoxy-1(2H)-quinolinecarboxylic acid benzyl ester is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

30831-75-5

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30831-75-5 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 30831-75-5 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 3,0,8,3 and 1 respectively; the second part has 2 digits, 7 and 5 respectively.
Calculate Digit Verification of CAS Registry Number 30831-75:
(7*3)+(6*0)+(5*8)+(4*3)+(3*1)+(2*7)+(1*5)=95
95 % 10 = 5
So 30831-75-5 is a valid CAS Registry Number.
InChI:InChI=1/C18H17NO3/c1-21-17-12-11-15-9-5-6-10-16(15)19(17)18(20)22-13-14-7-3-2-4-8-14/h2-12,17H,13H2,1H3

30831-75-5SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 14, 2017

Revision Date: Aug 14, 2017

1.Identification

1.1 GHS Product identifier

Product name benzyl 2-methoxy-2H-quinoline-1-carboxylate

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:30831-75-5 SDS

30831-75-5Downstream Products

30831-75-5Relevant academic research and scientific papers

Direct enantioselective vinylogous Mannich-type reactions of acyclic enals: New experimental insights into the E/Z-dilemma

Vargiu, Michela,Favero, Lucilla,Menichetti, Andrea,Di Bussolo, Valeria,Marchetti, Fabio,Pescitelli, Gennaro,Di Pietro, Sebastiano,Pineschi, Mauro

, p. 522 - 533 (2019)

The direct heterofunctionalization of acyclic α,β-unsaturated aldehydes with N-acylquinolinium ions contemplating the formation of two stereocentres is studied using dienamine catalysis. This work gives some new experimental insights on the remote stereocontrol in dienamine catalysis using unbiased aliphatic systems and large electrophiles, pointing to a (Z)-preference of the reactive configuration of the second double bond.

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