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100553-75-1

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100553-75-1 Usage

Physical state

Colorless to pale yellow liquid

Odor

Fishy or ammonia-like

Uses

a. Complexing agent in analytical chemistry
b. Chelating agent in metal purification
c. Production of agrochemicals
d. Production of pharmaceuticals
e. Production of dyes
f. Manufacture of adhesives
g. Manufacture of sealants
h. Production of rubber chemicals
i. Used in fuel and oil additives

Safety precautions

Corrosive, can cause skin and eye irritation, respiratory issues, and other health hazards

Check Digit Verification of cas no

The CAS Registry Mumber 100553-75-1 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,0,0,5,5 and 3 respectively; the second part has 2 digits, 7 and 5 respectively.
Calculate Digit Verification of CAS Registry Number 100553-75:
(8*1)+(7*0)+(6*0)+(5*5)+(4*5)+(3*3)+(2*7)+(1*5)=81
81 % 10 = 1
So 100553-75-1 is a valid CAS Registry Number.

100553-75-1SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 16, 2017

Revision Date: Aug 16, 2017

1.Identification

1.1 GHS Product identifier

Product name N'-(pyridin-3-ylmethyl)ethane-1,2-diamine

1.2 Other means of identification

Product number -
Other names 1-(3-pyridinylmethyl)-1,2-diaminoethane

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:100553-75-1 SDS

100553-75-1Relevant articles and documents

Design, synthesis, and bioactivity of cyanonitrovinyl neonicotinoids as potential insecticides

Wang, Kewei,Qian, Xuhong,Cui, Jingnan

scheme or table, p. 1117 - 1122 (2012/06/18)

A series of cyanonitrovinyl neonicotinoids were designed and synthesized via five steps in about 35% overall yields. All compounds were structurally characterized by 1H nuclear magnetic resonance (NMR), 13C NMR, infrared (IR), and high-resolution mass spectrometry (HRMS), and single-crystal X-ray diffraction analysis of 2-[1-[(6-chloropyridin-3-yl)methyl] -2-imidazolidinylidene]-2-nitroacetonitrile revealed that the double bond is (E)-configured. The preliminary agriculture bioassay indicated that one compound exhibited moderate insecticidal activity against pea aphid. Springer-Verlag 2010.

Design, synthesis, and evaluation of unsymmetrical difluoro-boron complexes with imidazoline as potential fungicides

Wang, Kewei,Cui, Jingnan,Xie, Lijuan,Qian, Xuhong

experimental part, p. 418 - 424 (2010/08/05)

A series of unsymmetrical difluoroboron (BF2) complexes with pyridine and imidazoline were synthesized by reaction of new chelating ligands (arylmethyl-imidazolidinylidene)-pyridin-2-yl-amine with boron trifluoride diethyl etherate. All the ligands and BF2 complexes were structurally characterized by IR, HRMS, 1H, 13C, 11B, and 19F NMR,indicating the bidentate complexation of imidazoline nitrogen and the pyridine nitrogen to the boron center. Evaluation of agricultural bioactivities showed that some of the BF2 complexes exhibited moderate fungicidal activities, and most of the BF2 complexes exhibited higher activities than the none-BF2 complexed substrates.

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