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2-BENZYL-2H-PYRAZOLE-3-CARBALDEHYDE is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

102808-00-4

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102808-00-4 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 102808-00-4 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,0,2,8,0 and 8 respectively; the second part has 2 digits, 0 and 0 respectively.
Calculate Digit Verification of CAS Registry Number 102808-00:
(8*1)+(7*0)+(6*2)+(5*8)+(4*0)+(3*8)+(2*0)+(1*0)=84
84 % 10 = 4
So 102808-00-4 is a valid CAS Registry Number.
InChI:InChI=1/C11H10N2O/c14-9-11-6-7-12-13(11)8-10-4-2-1-3-5-10/h1-7,9H,8H2

102808-00-4SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 18, 2017

Revision Date: Aug 18, 2017

1.Identification

1.1 GHS Product identifier

Product name 2-benzylpyrazole-3-carbaldehyde

1.2 Other means of identification

Product number -
Other names 2-BENZYL-2H-PYRAZOLE-3-CARBALDEHYDE

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:102808-00-4 SDS

102808-00-4Upstream product

102808-00-4Relevant academic research and scientific papers

Synthesizing process of nitrogen-heterocyclic high-selectivity aldehyde

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Paragraph 0014; 0022; 0023; 0035; 0039; 0048; 0052, (2017/09/05)

The invention relates to a synthesizing process of nitrogen-heterocyclic high-selectivity aldehyde. The synthesizing process is characterized in that when nitrogen-heterocyclic nitrogen atoms have hydrogen atoms, pyrrole, piperidine and pyrazole are used as the initial raw materials, and the pyrrole, the piperidine and the pyrazole are allowed to have reaction with piperidine-1-formaldehyde under nitrogen atom protection to obtain required nitrogen-atom ortho-position aldehyde; when nitrogen-heterocyclic nitrogen atoms have no hydrogen atoms, pyridine and pyrimidine are used to have reaction with the piperidine-1-formaldehyde to obtain the required nitrogen-atom ortho-position aldehyde. The synthesizing process is simple to operate, few in steps and high in selectivity and is a universal method using nitrogen heterocycle to synthesize the nitrogen ortho-position aldehyde.

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