Welcome to LookChem.com Sign In|Join Free
  • or
Quinoline, 2-ethyl-1,2,3,4-tetrahydro- is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

42835-88-1

Post Buying Request

42835-88-1 Suppliers

Recommended suppliers

  • Product
  • FOB Price
  • Min.Order
  • Supply Ability
  • Supplier
  • Contact Supplier

42835-88-1 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 42835-88-1 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 4,2,8,3 and 5 respectively; the second part has 2 digits, 8 and 8 respectively.
Calculate Digit Verification of CAS Registry Number 42835-88:
(7*4)+(6*2)+(5*8)+(4*3)+(3*5)+(2*8)+(1*8)=131
131 % 10 = 1
So 42835-88-1 is a valid CAS Registry Number.

42835-88-1SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 17, 2017

Revision Date: Aug 17, 2017

1.Identification

1.1 GHS Product identifier

Product name 2-Ethyl-1,2,3,4-tetrahydroquinoline

1.2 Other means of identification

Product number -
Other names 2-ethyl-1,1-diphenylthiocyclobutane

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:42835-88-1 SDS

42835-88-1Downstream Products

42835-88-1Relevant academic research and scientific papers

Synthesis of Tetrahydroquinolines via Borrowing Hydrogen Methodology Using a Manganese PN3Pincer Catalyst

Hofmann, Natalie,Homberg, Leonard,Hultzsch, Kai C.

, p. 7964 - 7970 (2020)

A straightforward and selective synthesis of 1,2,3,4-tetrahydroquinolines starting from 2-aminobenzyl alcohols and simple secondary alcohols is reported. This one-pot cascade reaction is based on the borrowing hydrogen methodology promoted by a manganese(I) PN3 pincer complex. The reaction selectively leads to 1,2,3,4-tetrahydroquinolines thanks to a targeted choice of base. This strategy provides an atom-efficient pathway with water as the only byproduct. In addition, no further reducing agents are required.

Post a RFQ

Enter 15 to 2000 letters.Word count: 0 letters

Attach files(File Format: Jpeg, Jpg, Gif, Png, PDF, PPT, Zip, Rar,Word or Excel Maximum File Size: 3MB)

1 Customer Service

What can I do for you?
Get Best Price

Get Best Price for 42835-88-1