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4-Pyridinecarboxamide,N-2-propynyl-(9CI) is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

680584-61-6

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680584-61-6 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 680584-61-6 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 6,8,0,5,8 and 4 respectively; the second part has 2 digits, 6 and 1 respectively.
Calculate Digit Verification of CAS Registry Number 680584-61:
(8*6)+(7*8)+(6*0)+(5*5)+(4*8)+(3*4)+(2*6)+(1*1)=186
186 % 10 = 6
So 680584-61-6 is a valid CAS Registry Number.

680584-61-6SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 20, 2017

Revision Date: Aug 20, 2017

1.Identification

1.1 GHS Product identifier

Product name N-prop-2-ynylpyridine-4-carboxamide

1.2 Other means of identification

Product number -
Other names N-(prop-2-yn-1-yl)aniline hydrochloride

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:680584-61-6 SDS

680584-61-6Relevant articles and documents

Synthesis of gibberellic acid derivatives and their effects on plant growth

Tian, Hao,Xu, Yiren,Liu, Shaojin,Jin, Dingsha,Zhang, Jianjun,Duan, Liusheng,Tan, Weiming

supporting information, (2017/06/08)

A series of novel C-3-OH substituted gibberellin derivatives bearing an amide group were designed and synthesized from the natural product gibberellic acid (GA3). Their activities on the plant growth regulation of rice and Arabidopsis were evaluated in vivo. Among these compounds, 10d and 10f exhibited appreciable inhibitory activities on rice (48.6% at 100 μmol/L) and Arabidopsis (41.4% at 100mol/L), respectively. These results provide new insights into the design and synthesis of potential plant growth regulators.

Zn-catalyzed hydrohydrazination of propargylamides with BocNHNH2: A novel entry into the 1,2,4-triazine core

Lukin, Alexey,Vedekhina, Tatiana,Tovpeko, Dmitry,Zhurilo, Nikolay,Krasavin, Mikhail

, p. 57956 - 57959 (2016/07/07)

Hydrohydrazination of a variety of propargylamides with BocNHNH2 under Zn(OTf)2 catalysis, unexpectedly, gave dihydro-1,2,4-triazines with a loss of the protecting group. The initial products can be efficiently aromatized in situ wit

Metal-coordinated water-soluble cavitands act as C - H oxidation catalysts

Djernes, Katherine E.,Moshe, Orly,Mettry, Magi,Richards, Donald D.,Hooley, Richard J.

supporting information; experimental part, p. 788 - 791 (2012/05/04)

Cavitands can be smoothly derivatized by CuAAC chemistry to incorporate ligand species at the upper rim. These species can coordinate metal species in a number of different conformations, leading to self-assembly. The metal-coordination confers water solu

Surprising alteration of antibacterial activity of 5″-modified neomycin against resistant bacteria

Zhang, Jianjun,Chiang, Fang-I.,Wu, Long,Czyryca, Przemyslaw Greg,Li, Ding,Chang, Cheng-Wei Tom

experimental part, p. 7563 - 7573 (2009/12/07)

A facile synthetic protocol for the production of neomycin B derivatives with various modifications at the 5″ position has been developed. The structural activity relationship (SAR) against aminoglycoside resistant bacteria equipped with various aminoglycoside-modifying enzymes (AMEs) was investigated. Enzymatic and molecular modeling studies reveal that the superb substrate promiscuity of AMEs allows the resistant bacteria to cope with diverse structural modifications despite the observation that several derivatives show enhanced antibacterial activity compared to the parent neomycin. Surprisingly, when testing synthetic neomycin derivatives against other human pathogens, two leads exhibit prominent activity against both methicillin-resistant Staphylococcus aureus (MRSA) and vancomycin-resistant enterococci (VRE) that are known to exert a high level of resistance against clinically used aminoglycosides. These findings can be extremely useful in developing new aminoglycoside antibiotics against resistant bacteria. Our result also suggests that new biological and antimicrobial activities can be obtained by chemical modifications of old drugs.

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