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5,7-Dichloro-8-nitroquinoline is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

34522-74-2

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34522-74-2 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 34522-74-2 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 3,4,5,2 and 2 respectively; the second part has 2 digits, 7 and 4 respectively.
Calculate Digit Verification of CAS Registry Number 34522-74:
(7*3)+(6*4)+(5*5)+(4*2)+(3*2)+(2*7)+(1*4)=102
102 % 10 = 2
So 34522-74-2 is a valid CAS Registry Number.

34522-74-2SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 18, 2017

Revision Date: Aug 18, 2017

1.Identification

1.1 GHS Product identifier

Product name 5,7-dichloro-8-nitro-quinoline

1.2 Other means of identification

Product number -
Other names 5,7-Dichlor-8-nitro-chinolin

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:34522-74-2 SDS

34522-74-2Relevant academic research and scientific papers

Use of a readily removable auxiliary group for the synthesis of pyrrolidones by the palladium-catalyzed intramolecular amination of unactivated γ C(sp3)-H Bonds

He, Gang,Zhang, Shu-Yu,Nack, William A.,Li, Qiong,Chen, Gong

supporting information, p. 11124 - 11128 (2013/10/22)

Easy on, easy off: Directing groups found to promote the palladium-catalyzed amination of γ C(sp3)-H and C(sp 2)-H bonds of secondary amides included 5-methoxy-8-aminoquinoline, which can be removed under mild conditions (see scheme; CAN=ceric ammonium nitrate). In conjunction with a β-C-H methylation or γ-C-H arylation step, the γ-C(sp3)-H amination provided access to complex pyrrolidones from readily available precursors. Copyright

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