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16322-14-8

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16322-14-8 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 16322-14-8 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 1,6,3,2 and 2 respectively; the second part has 2 digits, 1 and 4 respectively.
Calculate Digit Verification of CAS Registry Number 16322-14:
(7*1)+(6*6)+(5*3)+(4*2)+(3*2)+(2*1)+(1*4)=78
78 % 10 = 8
So 16322-14-8 is a valid CAS Registry Number.
InChI:InChI=1/C12H13NO2/c1-2-15-12(14)13-9-5-7-10-6-3-4-8-11(10)13/h3-8H,2,9H2,1H3

16322-14-8SDS

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 ethyl 2H-quinoline-1-carboxylate

1.2 Other means of identification

Product number -
Other names Quinoline,1-carbethoxy-1,2-dihydro

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:16322-14-8 SDS

16322-14-8Downstream Products

16322-14-8Relevant articles and documents

Enantioselective Synthesis of 4-Aminotetrahydroquinolines via 1,2-Reductive Dearomatization of Quinolines and Copper(I) Hydride-Catalyzed Asymmetric Hydroamination

Xu-Xu, Qing-Feng,Zhang, Xiao,You, Shu-Li

supporting information, p. 5357 - 5362 (2019/09/06)

A 1,2-reductive dearomatization of quinolines and copper(II) acetate monohydrate/(R,R)-Ph-BPE/P(p-tolyl)3-catalyzed enantioselective hydroamination sequence was developed, affording diverse 4-amino-1,2,3,4-tetrahydroquinolines with high levels of enantioselectivity in either a stepwise or one-pot fashion. Pleasingly, internal cis-cyclic alkenes, which are challenging substrates in copper hydride-catalyzed enantioselective hydroamination reactions, were transformed efficiently under mild conditions.

Depressant 1,2-dihydroquinolines and related derivatives.

Muren,Weissman

, p. 49 - 53 (2007/10/07)

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