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2-Pyridinamine,3-(1-methylethenyl)-(9CI) is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

213666-98-9

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213666-98-9 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 213666-98-9 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 2,1,3,6,6 and 6 respectively; the second part has 2 digits, 9 and 8 respectively.
Calculate Digit Verification of CAS Registry Number 213666-98:
(8*2)+(7*1)+(6*3)+(5*6)+(4*6)+(3*6)+(2*9)+(1*8)=139
139 % 10 = 9
So 213666-98-9 is a valid CAS Registry Number.

213666-98-9SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 15, 2017

Revision Date: Aug 15, 2017

1.Identification

1.1 GHS Product identifier

Product name 3-Isopropenyl-2-pyridinamine

1.2 Other means of identification

Product number -
Other names 9,10-Anthracenedione,2-amino-3-iodo

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:213666-98-9 SDS

213666-98-9Downstream Products

213666-98-9Relevant academic research and scientific papers

Novel complex n-heterocycles via intramolecular 1,5-electrocyclizations: l,2,4,4a,5,5a,10-octahydropyrido[4",3":2',3']cyclobuta[1',2':4,5] pyrrolo[2,3-b]pyridines

Walter, Harald,Sundermann, Garsten

, p. 1581 - 1591 (1998)

The synthesis of 2-amino-3-isopropenylpyridine (5) and 2-amino-5-chloro-3-isopropenylpyridine (6) and their toluenesulfonic acid catalyzed reactions in refluxing toluene with some 1-substituted piperidin-4-ones are described. The toluenesulfonic acid cata

Nickel/Photo-Cocatalyzed Asymmetric Acyl-Carbamoylation of Alkenes

Fan, Pei,Lan, Yun,Zhang, Chang,Wang, Chuan

, p. 2180 - 2186 (2020/03/03)

An unprecedented asymmetric acyl-carbamoylation of pendant alkenes tethered on aryl carbamic chlorides with both aliphatic and aromatic aldehydes has been developed via the cooperative catalysis of a chiral nickel-PHOX complex and tetrabutylammonium decatungstate. This reaction represents the first example of merging hydrogen-atom-transfer photochemistry and asymmetric transition metal catalysis in difunctionalization of alkenes. Using this protocol, a variety of oxindoles bearing a challenging quaternary stereogenic center are furnished under mild conditions in highly enantioselective manner.

KRAS G12C INHIBITORS AND METHODS OF USING THE SAME

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Paragraph 0652, (2019/11/19)

Provided herein are KRAS G12C inhibitors, composition of the same, and methods of using the same. These inhibitors are useful for treating a number of disorders, including pancreatic, colorectal, and lung cancers.

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