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70826-06-1

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70826-06-1 Usage

Type of compound

chemical compound

Use

often used as a ligand in coordination chemistry

Bidentate

capable of forming coordination complexes with metal ions by donating two electron pairs

Potential applications

studied for its potential applications in catalysis and materials science

Toxicity

can be toxic if proper precautions are not taken

Hazards

may cause irritation to the skin, eyes, and respiratory tract

Check Digit Verification of cas no

The CAS Registry Mumber 70826-06-1 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 7,0,8,2 and 6 respectively; the second part has 2 digits, 0 and 6 respectively.
Calculate Digit Verification of CAS Registry Number 70826-06:
(7*7)+(6*0)+(5*8)+(4*2)+(3*6)+(2*0)+(1*6)=121
121 % 10 = 1
So 70826-06-1 is a valid CAS Registry Number.

70826-06-1SDS

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-N,6-N-bis(pyridin-2-ylmethyl)pyridine-2,6-diamine

1.2 Other means of identification

Product number -
Other names N,N'-di(2-pyridylmethylene)-2,6-diaminopyridine

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:70826-06-1 SDS

70826-06-1Relevant articles and documents

THERMAL REARRANGEMENTS OF 2,6-DI(PYRIDYLMETHYLENEAMINO)PYRIDINES INTO 3,5-DIPYRIDYLMETHYLENE-2,6-DIAMINOPYRIDINES

Kowalski, Piotr,Czuba, Wladyslaw

, p. 1184 - 1190 (2007/10/02)

Novel results obtained during thermal rearrangement studies on N,N'-dipyridylmethylene-2,6-diaminopyridines are reported.Formation of derivatives with pyridylmethylene groups at positions 3 and 5, together with N-pyridylmethylene-2,6-diaminopyridynes in reaction of 2,6-diaminopyridine with 2- or 4-pyridylmethanols has been staded.

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