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15192-56-0

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15192-56-0 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 15192-56-0 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 1,5,1,9 and 2 respectively; the second part has 2 digits, 5 and 6 respectively.
Calculate Digit Verification of CAS Registry Number 15192-56:
(7*1)+(6*5)+(5*1)+(4*9)+(3*2)+(2*5)+(1*6)=100
100 % 10 = 0
So 15192-56-0 is a valid CAS Registry Number.

15192-56-0SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 19, 2017

Revision Date: Aug 19, 2017

1.Identification

1.1 GHS Product identifier

Product name 2-[N-(diphenylmethyl)formimidoyl]-pyridine

1.2 Other means of identification

Product number -
Other names (E)-N-(pyridin-2-ylmethylene)benzhydrylamine

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:15192-56-0 SDS

15192-56-0Relevant articles and documents

An unsymmetrical binuclear iminopyridine-iron complex and its catalytic isoprene polymerization

Wang, Liang,Wang, Xiaowu,Hou, Hongbin,Zhu, Guangqian,Han, Zhenyu,Yang, Weiying,Chen, Xiao,Wang, Qinggang

, p. 8846 - 8849 (2020)

A series of chloride-bridged unsymmetrical mixed Fe(ii)-HS/Fe(ii)-LS binuclear structures has been prepared and characterized. Upon activation with MAO, highly efficient catalytic polymerization of isoprene was achieved, delivering an ultra-high molecular

An enantioselective CpRu-catalyzed carroll rearrangement

Constant, Samuel,Tortoioli, Simone,Mueller, Jessica,Lacour, Jerome

, p. 2082 - 2085 (2007)

(Chemical Equation Presented) Simple ligands, catalyst, and conditions: The combination of readily prepared unsymmetrical pyridine-imine ligands and [CpRu(CH3CN)3][PF6] (Cp = C5H 5) affords regio- and

Paclitaxel Biosynthesis: Adenylation and Thiolation Domains of an NRPS TycA PheAT Module Produce Various Arylisoserine CoA Thioesters

Muchiri, Ruth,Walker, Kevin D.

, p. 1415 - 1425 (2017/03/23)

Structure-activity relationship studies show that the phenylisoserinyl moiety of paclitaxel (Taxol) is largely necessary for the effective anticancer activity. Several paclitaxel analogues with a variant isoserinyl side chain have improved pharmaceutical

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